Method for detecting microorganisms

Abstract

The present invention pertains to a method for detecting microorganisms such as mycoplasma or mouse minute virus (MMV) in a sample, the method comprising: (i) performing PCR on a sample suspected of comprising mycoplasma DNA with a PCR reaction mixture comprising (1) a first primer (Pl) annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 1 and a second primer (P2) annealing to a nucleic acid sequence of SEQ ID NO: 2, or (2) a third primer (P3) annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 109 and a fourth primer (P4) annealing to a nucleic acid sequence of SEQ ID NO: 110; and (ii) detecting a PCR product, wherein the detection of a PCR product indicates that the sample comprises microroganisms, and the absence of a PCR product indicates that the sample does not comprise microroganisms. The present invention further pertains to a pair of primers for detecting mycoplasma or virus in a sample, and to a kit for detecting mycoplasma or virus in a sample.

Description

[0001] International Patent Application under the PCT Applicant: Sanofi ZSP Ref: 589-385 PCT Method for detecting microorganisms The present invention relates to a method for detecting microorganisms, for examplemycoplasma or mouse minute virus (MMV), in a sample by performing PCR with specific primersand optionally additional probes. The present invention also provides primer pairs and a kit forperforming the method. Background of the invention Cell lines used for the manufacturing of drug substances intended for clinical trial orcommercial use must be tested and cleared from contamination by mircoorganisms, for examplemycoplasma or parvoviruses (see European Pharmacopoeia and ICH Guideline Q5 on viral safety).Besides mandatory testing requested by health authorities, it is in the interest of industries to perform regular testing in order to protect facilities from contamination by testing samples prior to theirintroduction into production facilities, and to detect contamination early on and protect downstreamequipment. Several methods can be used to document the status of cell substrates in terms ofmicroorganism contamination, such as mycoplasma or virus contamination, which mainly includesample cultivation in medium suitable for microorganism growth and colony identification and nucleic acid technologies (NAT) such as quantitative PCR (qPCR) and droplet digital PCR ddPCR for thedetection of bacterial or viral genetic material derived for example from mycoplasma or parvovirus.Because of the diversity of e.g. mycoplasma strains, health agencies expect assays to be able to detect a sub group of germs, based on their frequency and concerns for human health. Mouse minute virus (MMV), alternately known as Minute Virus of Mice, is a member of theparvovirus family and is a non-enveloped virus approximately 20 nm in diameter. MMV contains asingle-stranded DNA that is roughly 5 kb in size, and 2 genes ns1 (Non Structural 1) and vp1 (ViralProtein 1). There are four strains of MMV (i, p, m and c) and seven genomic sequences reported in theNCBI database. MMV is known to have contaminated production processes at multiple companiesthrough extrinsic sources. MMV can infect humans, although it is not considered a significant risk to operators and patient safety. However, the risk to the production process is significant as an MMVcontamination will likely result in the disruption of supply to patients, loss of product, costs ofcleaning facilities and equipment, and the potential disposal of expensive chromatography resin. Cell culture-based methods are difficult to implement due to the necessity to use optimal cell growth medium where all mycoplasma strains mentioned in guidelines, as well as parvoviruses, suchas MMV, might grow. In addition, due to the slow replication of mycoplasma, the completion of theseassays can take up to several weeks during which contamination from external sources might happenand lead to false positive results and long investigations. These assays are therefore outsourced tocontract manufacturing organizations but their long turn-around times are not compatible with shorttimelines required in development and manufacturing, where products should be released with nodelays. NAT represents an interesting alternative solution to cell culture-based techniques. BecausePCR devices are commonly found in all labs, many kits have been developed that guarantee detectionof microorganisms, for example mycoplasma contamination or MMV contamination with limit ofdetection (LOD) matching guidelines’ requirements. Existing solutions, however, rely on complex andsuboptimal designs. For example, because the assays must be able to detect different mycoplasma strains, some kits require the use of several primer sets specific to each strain. The use of SYBR green in kits, that allows for the detection of amplicons, is also a concern in the sense that non-specific DNA amplification might be detected and lead to false positive signals and trigger long investigationcampaigns. This was confirmed recently in Applicant’s own lab where the analysis with theMycoTOOL kit (Roche) of a sample contaminated with bacteria, but no mycoplasma, returnedpositive results. The present invention therefore addresses the need for an easy, fast and cost-effective method for detecting microorganisms, such as mycoplasma or virus contaminations in a sample. The methodallows for highly specific and sensitive detection of microorganisms, such as mycoplasma or virus byusing novel primers targeting mycoplasma regions not targeted before.Summary of the invention The objective underlying the present invention is solved by the provision of a method fordetecting microorganisms in a sample, comprising: (i) performing PCR on a sample suspected of comprising mycoplasma DNA with a PCR reaction mixture comprising (1) a first primer (P1) annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 1 and a second primer (P2) annealing to a nucleic acid sequence of SEQ ID NO: 2; or (2) a third primer (P3) annealing to thereverse complement of a nucleic acid sequence of SEQ ID NO: 109 and a fourth primer (P4) annealingto a nucleic acid sequence of SEQ ID NO: 110; and (ii) detecting a PCR product, wherein thedetection of a PCR product indicates that the sample comprises microorganisms, and wherein theabsence of a PCR product indicates that the sample does not comprise microorganisms. According to one aspect, the present invention provides a method for detecting mycoplasma in a sample, comprising: (i) performing PCR on a sample suspected of comprising mycoplasma DNA with a PCR reaction mixture comprising a first primer (P1) annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 1 and a second primer (P2) annealing to a nucleic acid sequenceof SEQ ID NO: 2; and (ii) detecting a PCR product, wherein the detection of a PCR product indicatesthat the sample comprises mycoplasma, and the absence of a PCR product indicates that the sample does not comprise mycoplasma.According to one embodiment, (i) P1 has a length between 18 and 24 nucleotides, preferablybetween 19 and 21 nucleotides and most preferably 19 nucleotides and / or P2 has a length between 17and 22 nucleotides preferably between 18 and 20 nucleotides, most preferably 20 nucleotides; and / or(ii) P1 has a Tm of between 60°C and 70°C, preferably between 63°C and 69°C, more preferablybetween 66°C and 68°C, and / or P2 has a Tm of between 60°C and 67°C, preferably of between 62 and66°C and most preferably between 64°C and 65°C; and / or (iii) P1 comprises or consists of a nucleicacid sequence of SEQ ID NO: 3 to 49 and / or P2 comprises or consists of a nucleic acid sequence of SEQ ID NO: 50 to 52. According to another embodiment, the reaction mixture further comprises at least a firstnucleic acid probe (Probe 1) annealing or binding to a nucleic acid sequence of SEQ ID NO: 53 or its reverse complement. According to one embodiment, (i) the reaction mixture further comprises at least a secondnucleic acid probe (Probe 2) annealing to SEQ ID NO: 53; and / or (ii) Probe 1 and / or Probe 2 each hasa length between 20 and 42 nucleotides, preferably between 21 and 30 nucleotides and most preferably22 and 24 nucleotides; and / or (iii) Probe 1 and / or Probe 2 each has a Tm of between 55°C and 70°C,preferably between 58°C and 69°C, more preferably between 59°C and 68°C; and / or (iv) Probe 1comprises or consists of a nucleic acid sequence of SEQ ID NO: 54 to 65 and / or Probe 2 comprises orconsists of a nucleic acid sequence of SEQ ID NO: 66; and / or (v) Probe 1 and / or Probe 2 eachcomprises one or more locked nucleic acids (LNA) and / or a minor grove binding (MGB) moiety;and / or (vi) Probe 1 and / or Probe 2 each comprises a detectable label, wherein preferably Probe 1 andProbe 2 comprise the same detectable label. According to one embodiment, (i) the PCR is qPCR, dPCR, ddPCR or cdPCR; and / or (ii) thePCR uses annealing temperature of between 55°C and 65°C, preferably between 58°C and 60°C;and / or (iii) the PCR comprises an activation step and / or a degradation step; and / or (iv) annealing andelongation are performed at the same temperature; and / or (v) the PCR comprises between 40 and 50cycles of denaturation and annealing / elongation, preferably 45 cycles. According to a preferred embodiment, the reaction mixture further comprises an internal positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleic acids of the nucleic acid sequenceof SEQ ID NO: 2, and between these two nucleic acid sequences an intervening nucleic acid sequenceof a length of at least 18 nucleotides, wherein the intervening nucleic acid sequence preferably differs from SEQ ID NO: 53 in that neither Probe 1 nor Probe 2 anneals to the intervening nucleic acidsequence, wherein the reaction mixture preferably further comprises at least a third nucleic acid probe(Probe 3) annealing to the intervening nucleic acid sequence or to its reverse complement. According to a further embodiment, i) Probe 3 has a length between 20 and 42 nucleotides,preferably between 21 and 30 nucleotides and most preferably 22 and 24 nucleotides; and / or (ii) Probe3 has a Tm of between 55°C and 70°C, preferably between 58°C and 69°C, more preferably between 59°C and 68°C; and / or (iii) Probe 3 comprises or consists of a nucleic acid sequence of SEQ ID NO: 69 or its reverse complement; and / or (iv) Probe 3 comprises one or more locked nucleic acids (ENA) and / or a minor grove binding (MGB) moiety; and / or (v) Probe 3 comprises a detectable label different from the label of Probe 1 and Probe 2.

[0002] According to a preferred embodiment, the internal positive control nucleic acid sequence comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 68 or its reverse complement.

[0003] According to yet another embodiment, the reaction mixture further comprises a discriminatory positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2 and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides, wherein the intervening nucleic acid sequence preferably does not differ from SEQ ID NO: 53 so that Probe 1 and Probe 2 are capable of annealing to the intervening nucleic acid sequence, wherein the reaction mixture preferably further comprises at least a fourth nucleic acid probe (Probe 4) annealing to the intervening nucleic acid sequence or to its reverse complement at a sequence that is different from the sequence to which Probe 1 and / or Probe 2 anneals.

[0004] According to an embodiment, i) Probe 4 has a length between 20 and 42 nucleotides, preferably between 21 and 30 nucleotides and most preferably 22 and 24 nucleotides; and / or (ii) Probe 4 has a Tm of between 55°C and 70°C, preferably between 58°C and 69°C, more preferably between 59°C and 68°C; and / or (iii) Probe 4 comprises or consists of a nucleic acid sequence of SEQ ID NO: 71 or its reverse complement; and / or (iv) Probe 4 comprises one or more locked nucleic acids (ENA) and / or a minor grove binding (MGB) moiety; and / or (v) Probe 4 comprises a detectable label different from the label of Probe 1, Probe 2, and Probe 3.

[0005] According to a preferred embodiment, the discriminatory positive control nucleic acid sequence comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 70 or its reverse complement.

[0006] According to yet another embodiment, the sample is a biological sample preferably selected from the group consisting of a cell bank, a cell culture, a culture medium, a cell culture supernatant, a medicinal product, a vaccine preparation, blood, saliva, and sputum.

[0007] According to yet another aspect, the present invention provides a pair of primers for detecting mycoplasma in a sample, comprising a primer Pl annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 1, and a primer P2 annealing to a nucleic acid sequence of SEQ ID NO: 2. According to a yet a further aspect, the present invention provides a kit for detecting mycoplasma in a sample, wherein the kit comprises the pair of primers of the present invention and a first nucleic acid probe (Probe 1) annealing to a nucleic acid sequence of SEQ ID NO: 53 or its reverse complement, and optionally a second nucleic acid probe (Probe 2) annealing to SEQ ID NO: 53 or itsreverse complement. The kit preferably further comprises one or more of (i) a PCR reaction mixture;(ii) an internal positive control nucleic acid sequence comprising at least 18 consecutive nucleic acidsof the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2 and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides, wherein the intervening nucleic acid sequence preferably differs from SEQ ID NO: 53 in that neither Probe 1 nor Probe 2 anneals to the intervening nucleic acid sequence, wherein the kit preferably further comprises at least a third nucleic acid probe(Probe 3) annealing to the intervening nucleic acid sequence or to its reverse complement; (iii) adiscriminatory positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2 and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 60 nucleotides, wherein the intervening nucleic acid sequence preferably does not differ from SEQ ID NO: 53 so that Probe 1 and Probe 2 are capable of annealing to the intervening nucleic acid sequence, wherein the kit preferably further comprises at least a fourth nucleic acid probe (Probe 4) annealing to the intervening nucleic acid sequence or to its reversecomplement that is different from the sequence to which Probe 1 and / or Probe 2 anneals; (iv) meansfor extracting and / or purifying DNA from the sample; (v) instructions for performing PCR with theprimers. According to one embodiment, in the method of the invention, in the pair of primers of the invention, or in the kit of the invention, the mycoplasma is one or more Mycoplasma species selected from the group consisting of Mycoplasma arginini, Mycoplasma buccale, Mycoplasma hominis, Mycoplasma orale, Mycoplasma salivarium, Mycoplasma fermentans, Mycoplasma hyorhinis, Mycoplasma synoviae, Mycoplasma pneumoniae, Acholeplasma laidlawii, Mycoplasma gallisepticumand Spiroplasma citri.According to a further aspect, the present invention provides a method for detecting virus in asample, comprising: (i) performing PCR on a sample suspected of comprising virus DNA with a PCRreaction mixture comprising a third primer (P3) annealing to the reverse complement of a nucleic acidsequence of SEQ ID NO: 109 and a fourth primer (P4) annealing to a nucleic acid sequence of SEQID NO: 110; and (ii) detecting a PCR product, wherein the detection of a PCR product indicates thatthe sample comprises virus, and the absence of a PCR product indicates that the sample does notcomprise virus. According to one embodiment, (i) P3 has a length between 20 and 25 nucleotides, preferably between 21 and 24 nucleotides and most preferably 23 nucleotides, and / or P4 has a length between 15 and 21 nucleotides preferably between 16 and 20 nucleotides, most preferably 23 nucleotides; and / or (ii) P3 has a Tm of between 60°C and 70°C, preferably between 63°C and 69°C, more preferably between 66°C and 68°C, and / or P4 has a Tm of between 60°C and 67°C, preferably of between 62 to66°C and most preferably between 64°C and 65°C; and / or (iii) P3 comprises or consists of a nucleic acid sequence of SEQ ID NO: 104, and / or P4 comprises or consists of a nucleic acid sequence of SEQ ID NO: 105. According to one embodiment, the reaction mixture further comprises at least one nucleic acid probe (Probe 5) annealing to a nucleic acid sequence of SEQ ID NO: 111 or its reverse complement. According to a further embodiment, (i) Probe 5 has a length between 15 and 30 nucleotides,preferably between 18 and 22 nucleotides and most preferably 19 and 21 nucleotides; and / or (ii) Probe5 has a Tm of between 59°C and 71°C, preferably between 60°C and 70°C, more preferably between63°C and 67°C; and / or (iii) Probe 5 comprises or consists of a nucleic acid sequence of SEQ ID NO:106; and / or (iv) Probe 5 comprises one or more locked nucleic acids (LNA) and / or a minor grove binding (MGB) moiety; and / or (v) Probe 5 comprises a detectable label. According to yet another embodiment, (i) the PCR is qPCR, dPCR, ddPCR or cdPCR; and / or (ii) the PCR uses an annealing temperature of between 55°C and 65°C, preferably between 58°C and 60°C; and / or (iii) the PCR comprises an activation step and / or a degradation step; and / or (iv) annealing and elongation are performed at the same temperature; and / or (v) the PCR comprises between 40 and 50 cycles of denaturation and annealing / elongation, preferably 45 cycles. According to a further embodiment, the reaction mixture further comprises an internal positivecontrol sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQID NO: 68 or 112 or 115.According to another embodiment, the internal positive control nucleic acid sequence comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence ofSEQ ID NO: 68 or 112 or 115, or its reverse complement.According to a further embodiment, the reaction mixture further comprises a discriminatorypositive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleicacid sequence of SEQ ID NO: 109 and at least 18 consecutive nucleic acids of the nucleic acidsequence of SEQ ID NO: 110 and between these two nucleic acid sequences an intervening nucleicacid sequence of a length of at least 18 nucleotides. According to an embodiment, the reaction mixture further comprises at least a third nucleic acid probe (Probe 3) and / or a fourth nucleic acid probe (Probe 4) annealing to the intervening nucleicacid sequence or to its reverse complement at a sequence that is different from the sequence to whichProbe 5 anneals. According to a preferred embodiment, Probe 3 has a length between 20 and 42 nucleotides,preferably between 21 and 30 nucleotides and most preferably 22 and 24 nucleotides, and / or has a Tmof between 55°C and 70°C, preferably between 58°C and 69°C, more preferably between 59°C and68°C, and / or comprises or consists of a nucleic acid sequence of SEQ ID NO: 69 or its reversecomplement, and / or comprises one or more locked nucleic acids (LNA) and / or a minor grove binding (MGB) moiety. According to a further preferred embodiment, Probe 4 has a length between 20 and 42 nucleotides, preferably between 21 and 30 nucleotides and most preferably between 22 and 24nucleotides, and / or has a Tm of between 55°C and 70°C, preferably between 58°C and 69°C, morepreferably between 59°C and 68°C, and / or comprises or consists of a nucleic acid sequence of SEQ IDNO: 71 or its reverse complement, and / or comprises one or more locked nucleic acids (LNA) and / or aminor grove binding (MGB) moiety, and / or comprises a detectable label different from the label ofProbe 3 and Probe 5.According to one embodiment, the discriminatory positive control nucleic acidsequence comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 113 or its reverse complement. According to one embodiment, the sample is a biological sample preferably selected from thegroup consisting of a cell bank, a culture medium, a cell culture, a cell culture supernatant, a medicinalproduct, a vaccine preparation, blood, saliva, and sputum. According to a further aspect, the present invention provides a pair of primers for detecting MMV in a sample comprising: a primer P3 annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 109, and a primer P4 annealing to a nucleic acid sequence of SEQ ID NO:110. Primer P3 preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 104.Primer P4 preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 105. According to a further aspect, the present invention provides a kit for detecting MMV in a sample, wherein the kit comprises the pair of primers of the invention and a nucleic acid probe (Probe 5) annealing to a nucleic acid sequence of SEQ ID NO: 111 or its reverse complement, preferably wherein the kit further comprises one or more of: (i) a PCR reaction mixture; (ii) an internal positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acidsequence of SEQ ID NO: 109 and at least 18 consecutive nucleic acids of the nucleic acid sequence ofSEQ ID NO: 110 and between these two nucleic acid sequences an intervening nucleic acid sequenceof a length of at least 18 nucleotides; (iii) a discriminatory positive control nucleic acid sequencecomprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 109 andat least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 110 and betweenthese two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 29nucleotides, wherein the intervening nucleic acid sequence preferably does not differ from SEQ IDNO: 111 so that Probe 5 is capable of annealing to the intervening nucleic acid sequence; (iv) meansfor extracting and / or purifying DNA from the sample; (v) instructions for performing PCR with theprimers. According to one embodiment, in the method according to the invention, in the pair of primersaccording to the invention or in the kit according to the invention, the virus is selected from the groupconsisting of Anelloviridae, Inoviridae, Parvoviridae, preferably Parvovirus, Erythovirus,Dependovirus, Amdovirus and Bocavirus, more preferably Parvovirus, and most preferably Mouse Minute Virus. Further aspects and embodiments of the invention will become apparent from the appending claims and the following detailed description. Description of the drawings The invention is further illustrated by the following figures and examples without being limited thereto. Fig. 1 illustrates the results of the search for 100 bp stretches with 80% homology inmycoplasma 16s rRNA sequences across species, where primers and probes could align and bind, respectively. The figure shows the similarity of RNA of all species tested with +1 denoting 100% similarity. Identified sequence stretches fulfilling the criteria are highlighted: in the upper row between about 500 and 600 bp, in the middle row at around 800 bp, and in the bottom row at around 1100 bp. Fig. 2 shows sequence details of the regions on which forward primers, reverse primers andprobes were designed. Sequences of the corresponding species were aligned by subgroup for clarity.A: all mycoplasma species. B: bacteria and mycoplasma species. C: Mycoplasma hyorhinis,prokaryotic and eukaryotic species. Fig. 3 shows the analysis of Fwd7 / Rev1* PCR products on mycoplasma DNA samples. A:PAGE 15% analysis of PCRs performed on reference DNA from the indicated organisms. B: meltingcurves (left panel) and peaks (right panel) of the PCR products.Fig. 4 shows a schematic positioning of primers and probes on control constructs. A: Positionsof primers and probes on the discriminatory positive control (DPC). B: Positions of primers andprobes on the internal positive control (IPC). Fig. 5 shows a comparison of MMV serotype genomes. Sequences from the MMVp, MMVi,MMVc & MMVm listed in Table 24 were aligned and similarities calculated.Fig. 6 shows the sequence details of the regions on which forward primers, reverse primersand probes were designed. Sequences were aligned by subgroup for clarity. A) all MMV serotypes; B)MMV and parvoviruses of interest; C) MMV and parvoviruses with higher sequence homology intarget region. Fig. 7 schematically shows the positioning of primers and probes on control constructs. A)Positions of primers and probes on the MMV discriminatory positive control (DPC). B) Positions ofprimers and probes on the internal positive control v2 (IPC MMV). C) Positions of primers and probeson the internal positive control v3 (IPC Myco / MMV). Fig. 8 shows the results of the amplification of various gDNA with MMV primer set using afirst PCR mix containing all the reagents for specific MMV detection. A) MMV and DPCamplification on FAM channel; B) DPC amplification only on HEX channel; C) IPC amplification forall samples on Cy5 channel. X-axis shows the fluorescence intensity and y-axis shows the number ofPCR cycles. Fig. 9 shows the results of the amplification of various gDNA with their own primer set usinga second PCR mix containing all the reagents for specific MMV detection. A) Human amplification onFAM channel; B) E. coli amplification on HEX channel; C) CHO amplification on Cy5 channel. X-axis shows the fluorescence intensity and y-axis shows the number of PCR cycles. Fig. 10 shows the visualization of amplification products in 15% PAGE using the twodifferent PCR mixes targeting MMV matrixes and other gDNA matrixes, respectively. A) relevantamplifications from MMV using PCR Mix 1; B) relevant amplifications from gDNA using PCR Mix 2. Fig. 11 is a representation of the calibration curve for two different data units. After datareformatting, a 10 Cq drift is observed meaning about 3Log10 difference in absolute value. List of sequences The sequences referred to herein are disclosed in detail in the accompanying sequence listing.Sequences of the present invention are also listed in the following table 1.Table 1: Examples of nucleic acid sequences of the present invention, all in 5’ → 3’ orientation.SEQName SequenceIDNO1 Region3 fw template GGAATTGACGGGRMYCCGCACAAGYGGTGGAKCATGTKGYTTAATTYGA2 Region3 rev template TGGTGCAYGGTTGTCGTCAGYTCGTGYCGTGAGRTGTT3 FwMyco1 CCGCACAAGCGGTGGAGCATGTGG4 FwMyco2 ACCCGCACAAGCGGTGG5 FwMyco3 ACCCGCACAAGCGGTG6 FwMyco4 CCCGCACAAGCGGTG7 FwMyco5 CCCGCACAAGCGGTGG8 FwMyco6 CCGCACAAGCGGTGGA9 FwMyco7 CACAAGCGGTGGAGCATGT10 FwMyco8 ACAAGCGGTGGAGCATGTG11 FwMyco9 ACAAGCGGTGGAGCATGTGG12 FwMyco10 CAAGCGGTGGAGCATGTG13 FwMyco11 AAGCGGTGGAGCATGTGG14 FwMyco12 CGGTGGAGCATGTGGTTTAATT15 FwMyco13 CACAAGTGGTGGAGCATGTG16 FwMyco14 CACAAGTGGTGGAGCATGTGG17 FwMyco15 CACAAGTGGTGGAGCATGTGGT18 FwMyco16 ACAAGTGGTGGAGCATGTG19 FwMyco17 ACAAGTGGTGGAGCATGTGG20 FwMyco18 ACAAGTGGTGGAGCATGTGGT21 FwMyco19 ACAAGTGGTGGAGCATGTGGTT22 FwMyco20 CAAGTGGTGGAGCATGTGG23 FwMyco21 CAAGTGGTGGAGCATGTGGT24 FwMyco22 CAAGTGGTGGAGCATGTGGTT25 FwMyco23 CAAGTGGTGGAGCATGTGGTTT26 FwMyco24 GCACAAGCGGTGGATCATG27 FwMyco25 GCACAAGCGGTGGATCATGTFwMyco26 CACAAGCGGTGGATCATGTFwMyco27 CACAAGCGGTGGATCATGTTFwMyco28 CACAAGCGGTGGATCATGTTGFwMyco29 ACAAGCGGTGGATCATGTTGFwMyco30 ACAAGCGGTGGATCATGTTGTFwMyco31 ACAAGCGGTGGATCATGTTGTTFwMyco32 CAAGCGGTGGATCATGTTGFwMyco33 CAAGCGGTGGATCATGTTGTFwMyco34 GCACAAGTGGTGGAGCATGTFwMyco35 GCACAAGTGGTGGAGCATGTTFwMyco36 GCACAAGTGGTGGAGCATGTTGFwMyco37 CACAAGTGGTGGAGCATGTFwMyco38 CACAAGTGGTGGAGCATGTTFwMyco39 CACAAGTGGTGGAGCATGTTGFwMyco40 CACAAGTGGTGGAGCATGTTGCFwMyco41 ACAAGTGGTGGAGCATGTTFwMyco42 ACAAGTGGTGGAGCATGTTGFwMyco43 ACAAGTGGTGGAGCATGTTGCFwMyco44 ACAAGTGGTGGAGCATGTTGCTFwMyco45 CAAGTGGTGGAGCATGTTGFwMyco46 CAAGTGGTGGAGCATGTTGCFwMyco47 CAAGTGGTGGAGCATGTTGCTRevMyco1* CTGACGACAACCATGCACCARevMyco2* ACGACAACCATGCACCARevMyco3* TGACGACAACCATGCACCARegion3 pb template AACCTTACCHRSDYTTGACATMYHBBGCRAWRBYDTRGARAYAHRDYNRGAGGYYAWCVBDDDKACAGSMyco1 ZEN GCAAAGCTATAGAGATATAGTGGAGGTTAACASMyco2 ZEN GCAAAGCTATAGAGATATAGTGGAGGTTAACSMyco3 ZEN CAAAGCTATAGAGATATAGTGGAGGTTAACASMyco4 ZEN CAAAGCTATAGAGATATAGTGGAGGTTAACAGAATGACAGSMyco4bis ZEN CAAAGCTATAGAGATATAGTGGAGGTTAACAGAGTGACAGSMyco5 LNA TATAGTGGAGGTTAACAGAATGSMyco5bis LNA TATAGTGGAGGTTAACAGAGTGSMyco5 TATAGTGGAGGTTAACAGAATGSMyco5bis TATAGTGGAGGTTAACAGAGTGSMyco6 TATAGAGATATAGTGGAGGTTAACAGAGTGSMyco7 TATAGAGATATAGTGGAGGTTAACAGASMyco8 TATAGAGATATAGTGGAGGTTAACAGSAcho1 TAAGTTCGGAGGCTAACAGATGTSAcho1 LNA TAAGTTCGGAGGCTAACAGATGTMyco IPC; MMV IPCCGTCATCGGATCTCGAGGACCTGGCTTTAGAGCCTTGGA v3 GCACACCAAATACTCCTGTTGCGGGCACTGCAGAAACC CAGAACACTGGGGAAGCTGGTTCCAAAGCCTGCCAAGA TGGTCAACTGAGCCCAACTTGGTTTCACAAGCGGTGGA GCATGTGACAGAGATCGAGGAGGATTTGAGAGGCGCCC GTCAAAAAGAAGTCCGTCACACGCAGTGATCCCGGCTG CTGCGTCACATTCTGATGATGTTCTTCCCGCTAAGACTT CAGCGAGCCGCTTGGTGCATGGTTGTCGTCAGTTTGAAC TTGGACTAAGGTACGATGGCGCCTCCAGCTAAAAGAGC TAAAAGAGGTAAGGGTTTAAGGGATGGTTGGTTGGTGG GGTATTAATGTTTAATTACCTGTTTTACAGGCCTGAAAT CACTTGGTTTTAGGTTGGGTGCCTCCTGGCTACAAGTAC CTGGGACCACGTStraA CGCAGTGATCCCGGCTGCTGMyco DPC CGTCATCGGATCTCGAGGACCTGGCTTTAGAGCCTTGGAGCACACCAAATACTCCTGTTGCGGGCACTGCAGAAACC CAGAACACTGGGGAAGCTGGTTCCAAAGCCTGCCAAGA TGGTCAACTGAGCCCAACTTGGTTTCACAAGCGGTGGA GCATGTGGTTTAATTTGAAGATACGCGTAGAACCTTACC CACTCTTGACATCTTCTGCAAAGCTATAGAGATATAGTG GAGGTTAACAGAATGATTTAAGTTCGGAGGCTAACAGA TGTATTCCGACTCGCAGAACCGGAACGATTGATGGTGC ATGGTTGTCGTCAGTTTGAACTTGGACTAAGGTACGATG GCGCCTCCAGCTAAAAGAGCTAAAAGAGGTAAGGGTTT AAGGGATGGTTGGTTGGTGGGGTATTAATGTTTAATTAC CTGTTTTACAGGCCTGAAATCACTTGGTTTTAGGTTGGG TGCCTCCTGGCTACAAGTACCTGGGACCACGTSAtPSY CCGACTCGCAGAACCGGAACGAFwMMV CAGAGATCGAGGAGGATTTGAGARevMMV GCGGCTCGCTGAAGTCTProbe MMV CGTGCTTCGGTGCGGAACCGFtraA12 GCGCCCGTCAAAAAGAAGTRtraA11 GCGGGAAGAACATCATCAGAAFwMMV template AAGCTGGTTCCAAAGCCTGCCAAGATGGTCAACTGAGCCCAACTTGGTCAGAGATCGAGGATTTGAGARevMMV template AGACTTCAGCGAGCCGCTGAACTTGGACTAAGMMV probe region AGCGTGCTTCGGTGCGGAACCGTTGAAGAMMV IPC v2 CAGAGATCGAGGAGGATTTGAGAGGCGCCCGTCAAAAAGAAGTCGTTTTTTTCCAAATTCACTCGTCTGAATATGCTT CGCCTGGCTCGCGCAGTGATCCCGGCTGCTGTTCTGATG ATGTTCTTCCCGCTTGAAGAAAGACTTCAGCGAGCCGCMMV DPC CAGAGATCGAGGAGGATTTGAGAGCGTGCTTCGGTGCGGAACCGTTGCCGACTCGCAGAACCGGAACGAAGAAAGA CTTCAGCGAGCCGCMMV DPC full length AAAGGTGCCAACTCCTATAAATTTACTAGGTTCGGCACGCTCACCATTCACGACACCGAAAAGTACGCCTCTCAGCC AGAACTATGCACTAACTCCACTTGCATCGGATCTCGAGG ACCTGGCTTTAGAGCCTTGGAGCACACCAAATACTCCTG TTGCGGGCACTGCAGAAACCCAGAACACTGGGGAAGCT GGTTCCAAAGCCTGCCAAGATGGTCAACTGAGCCCAAC TTGGTCAGAGATCGAGGAGGATTTGAGAGCGTGCTTCG GTGCGGAACCGTTGCCGACTCGCAGAACCGGAACGAAG AAAGACTTCAGCGAGCCGCTGAACTTGGACTAAGGTAC GATGGCGCCTCCAGCTAAAAGAGCTAAAAGAGGTAAGG GTTTAAGGGATGGTTGGTTGGTGGGGTATTAATGTTTAA TTACCTGTTTTACAGGCCTGAAATCACTTGGTTTTAGGT TGGGTGCCTCCTGGCTACAAGTACCTGGGACCAGGGIPCv2 full length AAAGGTGCCAACTCCTATAAATTTACTAGGTTCGGCACGCTCACCATTCACGACACCGAAAAGTACGCCTCTCAGCC AGAACTATGCACTAACTCCACTTGCATCGGATCTCGAGG ACCTGGCTTTAGAGCCTTGGAGCACACCAAATACTCCTG TTGCGGGCACTGCAGAAACCCAGAACACTGGGGAAGCT GGTTCCAAAGCCTGCCAAGATGGTCAACTGAGCCCAAC TTGGTCAGAGATCGAGGAGGATTTGAGAGGCGCCCGTC AAAAAGAAGTCGTTTTTTTCCAAATTCACTCGTCTGAAT ATGCTTCGCCTGGCTCGCGCAGTGATCCCGGCTGCTGTT CTGATGATGTTCTTCCCGCTTGAAGAAAGACTTCAGCGA GCCGCTGAACTTGGACTAAGGTACGATGGCGCCTCCAG CTAAAAGAGCTAAAAGAGGTAAGGGTTTAAGGGATGGT TGGTTGGTGGGGTATTAATGTTTAATTACCTGTTTT116 MMV IPC v3 CACAAGCGGTGGAGCATGTGACAGAGATCGAGGAGGATTTGAGAGGCGCCCGTCAAAAAGAAGTCCGTCACACGCA GTGATCCCGGCTGCTGCGTCACATTCTGATGATGTTCTT CCCGCTAAGACTTCAGCGAGCCGCTTGGTGCATGGTTGT CGTCAG SEQ ID NOs: 72 to 103 shown in the figures are listed in the sequence listing, as are SEQ IDNOs: 117 to 192.Detailed description of the inventionBefore the present invention is described in detail below, it is to be understood that thisinvention is not limited to the particular methodology, protocols and reagents described herein as thesemay vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and it is not intended to limit the scope of the present invention which will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art. Preferably, the terms used herein are defined as described in "A multilingual glossary ofbiotechnological terms: (IUPAC Recommendations)", Leuenberger, H.G.W, Nagel, B. and Klbl, H. eds. (1995), Helvetica Chimica Acta, CH-4010 Basel, Switzerland). Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. In the following passages, different aspects of the invention are defined in more detail. Each aspect so defined may be combined with anyother aspect or aspects unless clearly indicated to the contrary. Any feature indicated as beingoptional, preferred or advantageous may be combined with any other feature or features indicated as being optional, preferred or advantageous. In the following, the elements of the present invention will be described. These elements are listed with specific embodiments; however, it should be understood that they may be combined in any manner and in any number to create additional embodiments. The variously described examples and preferred embodiments should not be construed to limit the present invention to only the explicitly described embodiments. This description should be understood to support and encompass embodiments which combine the explicitly described embodiments with any number of the disclosed and / or preferred elements. Furthermore, any permutations and combinations of all described elements in this application should be considered disclosed by the description of the present application unless the context indicates otherwise. Several documents are cited throughout the text of this specification. Each of the documents cited herein (including all scientific publications, manufacturer's specifications, instructions etc.), whether supra or infra, is hereby incorporated by reference in its entirety. Definitions In the following, some definitions of terms frequently used in this specification are provided. These terms will, in each instance of its use, in the remainder of the specification have the respectively defined meaning and preferred meanings. As used in this specification and the appended claims, the singular forms "a", "an", and "the" include plural referents, unless the content clearly dictates otherwise. The term "nucleic acid" or "polynucleotide" as used in this specification comprises polymericor oligomeric macromolecules, or large biological molecules, essential for all known forms of life. Nucleic acids, which include DNA (deoxyribonucleic acid) and RNA (ribonucleic acid), are made from monomers known as nucleotides. Most naturally occurring DNA molecules consist of two complementary biopolymer strands coiled around each other to form a double helix. The DNA strand is also known as polynucleotides consisting of nucleotides. Each nucleotide is composed of a nitrogen- containing nucleobase as well as a monosaccharide sugar called deoxyribose or ribose and a phosphate group. Naturally occurring nucleobases comprise guanine (G), adenine (A), thymine (T), uracil (U) or cytosine (C). The nucleotides are joined to one another in a chain by covalent bonds between the sugar of one nucleotide and the phosphate of the next, resulting in an alternating sugar-phosphate backbone. If the sugar is deoxyribose, the polymer is DNA. If the sugar is ribose, the polymer is RNA. Typically, a polynucleotide is formed through phosphodiester bonds between the individual nucleotidemonomers. In the context of the present invention the term "nucleic acid" includes but is not limited toribonucleic acid (RNA), deoxyribonucleic acid (DNA), and mixtures thereof such as e.g. RNA-DNA hybrids (within one strand), as well as cDNA, genomic DNA, recombinant DNA, cRNA and mRNA. The nucleic acid can also be an artificial nucleic acid. Artificial nucleic acids include polyamide or peptide nucleic acid (PNA), morpholino and locked nucleic acid (LNA), as well as glycol nucleic acid (GNA) and threose nucleic acid (TNA). Each of these is distinguished from naturally-occurring DNA or RNA by changes to the backbone of the molecule. The nucleic acids can e.g. be synthesized chemically, e.g. in accordance with the phosphotriester method (see, for example, Uhlmann, E. & Peyman, A. (1990) Chemical Reviews, 90, 543-584). The term "nucleic acid" and "nucleic acid molecule" are used synonymously herein and areunderstood as well-accepted in the art, i.e. as single or double-stranded oligo- or polymers ofdeoxyribonucleotide or ribonucleotide bases or both. The term "nucleic acids" as used herein includes not only deoxyribonucleic acids (DNA) and ribonucleic acids (RNA), but also all other linear polymers in which the bases adenine (A), cytosine (C), guanine (G) and thymine (T) or uracil (U) are arranged in a corresponding sequence (nucleic acid sequence). The invention also comprises the corresponding RNA sequences (in which thymine is replaced by uracil), complementary sequences and sequences with modified nucleic acid backbone or 3 'or 5'-terminus. Nucleic acids in the form of DNA are however preferred. The nucleotide base symbols used throughout the present disclosure are in line with thesymbols according to the WIPO ST.26 standard, as outlined in the following table 2.Table 2: standard abbreviations for nucleotidesThe term "primer" has the meaning as it would be understood by the person of ordinary skill inthe field of genetics. It denotes a short single-stranded nucleic acid molecule usually having a length of between 18 and 24 nucleotides and being capable of binding to a target nucleic acid (also referred to as template) by annealing (hybridization with the template through Watson-Crick base pairing). The "percentage of sequence identity" is determined by comparing two optimally alignedsequences over a comparison window, wherein the portion of the sequence in the comparison windowcan comprise additions or deletions (i.e. gaps) as compared to the reference sequence (which does notcomprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical nucleic acid base or amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity. The term "identical" is used herein in the context of two or more nucleic acids to refer to twoor more sequences or subsequences that are the same, i.e. that comprise the same sequence ofnucleotides or amino acids. Sequences are "identical" to each other if they have a specified percentage of nucleotides or amino acid residues that are the same. According to the present invention, at least 90% identical includes at least at least at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% identity over the specified sequence, when compared and aligned for maximum correspondence over a comparison window, or designated region as measured using one of the following sequence comparison algorithms or by manual alignment and visual inspection. These definitions also refer to the complement of a test sequence.Accordingly, the term "at least XY% sequence identity" is used throughout the specification withregard to polynucleotide sequence comparisons. In the context of the present invention, a nucleic acid sequence having at least 90% sequence identity to a given SEQ ID NO or a nucleic acid sequencereverse complementary thereto thus preferably means that said nucleic acid has a sequence having atleast 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% sequence identity to the given SEQ ID NO or a nucleic acid sequence reverse complementary to said SEQ ID NO. The term "sequence comparison" is used herein to refer to the process wherein one sequenceacts as a reference sequence, to which test sequences are compared. When using a sequence comparison algorithm, test and reference sequences are entered into a computer, if necessary, subsequence coordinates are designated, and sequence algorithm program parameters are designated. Default program parameters are commonly used, or alternative parameters can be designated. The sequence comparison algorithm then calculates the percent sequence identities for the test sequences relative to the reference sequence, based on the program parameters. In case where two sequences are compared and the reference sequence is not specified in comparison to which the sequence identitypercentage is to be calculated, the sequence identity is to be calculated with reference to the longer ofthe two sequences to be compared, if not specifically indicated otherwise. If the reference sequence is indicated, the sequence identity is determined on the basis of the full length of the reference sequenceindicated by one of the SEQ ID NOs of the present invention, if not specifically indicated otherwise.Methods of alignment of sequences for comparison are well known in the art. Optimal alignment of sequences for comparison can be conducted, for example, by the local homology algorithm of Smith and Waterman (Adv. Appl. Math. 2:482, 1970), by the homology alignment algorithm of Needleman and Wunsch 1970, by the search for similarity method of Pearson andLipman 1988, by computerized implementations of these algorithms (e.g., GAP, BESTFIT, FASTA,and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Ausubel et al., Current Protocols in Molecular Biology (1995 supplement)). Algorithms suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which aredescribed in Altschul et al. (Nuc. Acids Res. 25:3389-402, 1977), and Altschul et al. (J. Mol. Biol.215:403-10, 1990), respectively. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information (http: / / www.ncbi.nlm.nih.gov / ). This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et al., supra). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always >0) and N (penalty score for mismatching residues; always <0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, an expectation (E) of 10, M=5, N=-4 and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength of 3, and expectation (E) of 10, and the BLOSUM62scoring matrix (see Henikoff and Henikoff, 1989) alignments (B) of 50, expectation (E) of 10, M=5,N=-4, and a comparison of both strands. The BLAST algorithm also performs a statistical analysis of the similarity between two sequences (see, e.g., Karlin and Altschul, Proc. Natl. Acad. Sci. USA 90:5873-87, 1993). One measure of similarity provided by the BLAST algorithm is the smallest sum probability (P(N)), which provides an indication of the probability by which a match between two nucleotide or amino acid sequences would occur by chance. For example, a nucleic acid is considered similar to a reference sequence if the smallest sum probability in a comparison of the test nucleic acid to the reference nucleic acid is less than about 0.2, typically less than about 0.01, and more typically less than about 0.001. The term “anneals to” as used herein refers to pairing of complementary sequences of single-stranded nucleic acids to form a double-stranded polynucleotide preferably under stringentconditions.The term "subject" as used herein, refers to an animal, preferably a mammal, mostpreferably a human. The term "melting temperature" or "Tm" as used herein refers to the temperature at which halfof the DNA strands are in the random coil or single-stranded (ssDNA) state. Tm depends on the lengthof the DNA molecule and its specific nucleotide sequence. In the present invention, the Tm of a givennucleotide sequence is calculated using the software PrimerExpress® 3.0 (Life TechnologiesCorporation) using standard settings, the software Geneious Prime 2023.2 (Dotmatics) using thesettings Monovalent ions 50 mM, Divalent ions 3 mM, Primer 200 nM, dNTP 0.8 mM, or the Primerdesign tools for PCR & qPCR (Integrated DNA Technologies) using the parameter set for qPCR:Monovalent ions 50 mM, Divalent ions 3 mM, Primer 200 nM, dNTP 0.8 mM, further using theSantaLucia 1998 thermodynamics & salt correction (SantaLucia, Proc Natl Acad Sci USA, 1998, Vol.95(4): 1460-1465), or the SantaLucia 1998 thermodynamics and the Owczarzy 2004 salt correction(Owczarzy et al., Biochemistry 2004, Vol.43(12): 3537-3554). Description of embodiments The present invention is in the field of microorganism detection, and provides a method fordetecting microorganisms such as mycoplasma or mouse minute virus, specific primers and probes, as well as kits for detecting microorganisms such as mycoplasma or mouse minute virus. In the experiments leading to the present invention, it was surprisingly found that although three regions of sufficient homology between mycoplasma species for primer and probe design wereidentified (Fig. 1), only one region turned out to be suitable for primer and probe design, which furtherrequired a widening to accommodate the forward primer, a probe, and the reverse primer. It was further surprisingly found that only one genomic region turned out to be suitable for primer and probedesign for detecting mouse minute virus (MMV). The present invention describes the identification ofthese specific regions for primer and probe design, which primers and probes can be used formycoplasma detection or MMV detection, optionally together with other probes for positive controland for internal control. The primers and probes of the invention guarantee a high degree of specificity(no detection of bacterial DNA, no detection of CHO DNA, no detection of Human DNA) andsensitivity as required by established guidelines, e.g. for detecting as little as 10 CFU / mL ofmycoplasma in a sample. Thus, the present invention provides a method for detecting microorganisms in a sample, themethod comprising the steps of (i) performing PCR on a sample suspected of comprisingmicroroganism DNA with a PCR reaction mixture comprising: (1) a first primer (P1) annealing to thereverse complement of a nucleic acid sequence of SEQ ID NO: 1 and a second primer (P2) annealing to a nucleic acid sequence of SEQ ID NO: 2, or (2) a third primer (P3) annealing to the reversecomplement of a nucleic acid sequence of SEQ ID NO: 109 and a fourth primer (P4) annealing to anucleic acid sequence of SEQ ID NO: 110; and (ii) detecting a PCR product. Since the method aims atdetecting microorganisms in the sample, the detection of a PCR product that was produced in the PCRreaction using the two primers of (1) and / or (2) indicates that the sample comprises microorgansims. Likewise, the absence of such a PCR product indicates that the sample does not comprise microorganisms such as mycoplasma and MMV. The sample used in the context of the present invention is preferably a biological sample.According to a preferred embodiment, the sample is selected from the group consisting of but notlimited to a sample from a cell bank, a culture medium (such as but not limited to a cell culture medium), a cell culture, a cell culture supernatant, a medicinal product, a vaccine preparation, and abody fluid such as blood, saliva or sputum. The sample can be used in the method of the presentinvention in essentially untreated form. For example, the sample can be derived or obtained from anarticle, object, item or a subject. The sample may be directly added to the reaction mixture without requiring any preceding purification steps. Methods for obtaining such a sample are well known to theskilled person. Alternatively, the sample can be pretreated before being added to the reaction mixture.Such a pretreatment may include methods for purifying or isolating DNA from the sample, which canthen be used in the method of the invention. The method of the present invention allows for detecting microorganisms, such as bacteria or virus in the sample. According to one aspect, the present invention provides a method for detecting mycoplasma in a sample, comprising: (i) performing PCR on a sample suspected of comprising mycoplasma DNAwith a PCR reaction mixture comprising a first primer (P1) annealing to the reverse complement of anucleic acid sequence of SEQ ID NO: 1 and a second primer (P2) annealing to a nucleic acid sequenceof SEQ ID NO: 2; and (ii) detecting a PCR product, wherein the detection of a PCR product indicatesthat the sample comprises mycoplasma, and the absence of a PCR product indicates that the sample does not comprise mycoplasma. This method allows for detecting bacteria in the sample, in particular mycoplasma selectedfrom the group consisting of Mycoplasma species Mycoplasma arginini, Mycoplasma buccale, Mycoplasma hominis, Mycoplasma orale, Mycoplasma salivarium, Mycoplasma fermentans, Mycoplasma hyorhinis, Mycoplasma synoviae, Mycoplasma pneumoniae, Acholeplasma laidlawii,Mycoplasma gallisepticum and Spiroplasma citri.According to a further aspect, the present invention provides a method for detecting virus in asample, comprising: (i) performing PCR on a sample suspected of comprising virus DNA with a PCRreaction mixture comprising a third primer (P3) annealing to the reverse complement of a nucleic acidsequence of SEQ ID NO: 109 and a fourth primer (P4) annealing to a nucleic acid sequence of SEQID NO: 110; and (ii) detecting a PCR product, wherein the detection of a PCR product indicates thatthe sample comprises virus, and the absence of a PCR product indicates that the sample does notcomprise virus. This method allows for detecting virus in the sample selected from the group consisting of single-stranded DNA virus, such as Anelloviridae, Inoviridae, Parvoviridae. The family of Parvoviridae can be further subdivided into Parvovirinae comprising Parvovirus, Erythovirus, Dependovirus, Amdovirus and Bocavirus. Preferably, the method of the present invention allows for the detection of Parvovirus, in particular of Mouse Minute Virus (MMV). The reaction mixture used for the PCR is not particularly limited to a specific type and may be selected by the person of ordinary skill in the art or by following the instructions of a manufacturer of a component of a PCR reaction mixture. A PCR reaction mixture typically contains in addition to theprimers and the DNA template a DNA polymerase, deoxynucleoside triphosphates (dNTPs), a buffersolution and bivalent cations such as Mg2+or Mn2+. Preferred characteristics of the primers P1 and P2 to be used in the context of the invention aredisclosed in the following.Primer P1 preferably has a length of between 18 and 24 nucleotides, such as 18, 19, 20, 21, 22,23 and 24 nucleotides, preferably between 19 and 23, 19 and 22, 19 and 21, or 19 and 20 nucleotides,and most preferably a length of 19 nucleotides. Primer P1 preferably has a melting temperature (Tm) of between 60°C and 70°C, such as60°C, 61°C, 62°C, 63°C, 64°C, 65°C, 66°C, 67°C, 68°C, 69°C and 70°C, preferably between 63°Cand 69°C, more preferably between 66°C to 68°C, and most preferably of 67°C.Primer P1 preferably comprises or consists of a nucleic acid sequence of SEQ ID NOs: 3 to49. More preferably, primer P1 comprises or consists of a nucleic acid sequence according to SEQ IDNO: 9. Most preferably, P1 consists of the nucleic acid sequence according to SEQ ID NO: 9.Primer P2 preferably has a length of between 17 and 22 nucleotides, such as 17, 18, 19, 20, 21and 22 nucleotides, preferably between 18 and 20 nucleotides, or 19 and 20 nucleotides, and mostpreferably a length of 20 nucleotides. Primer P2 preferably has a Tm of between of between 60°C to 67°C, such as 60°C, 61°C,62°C, 63°C, 64°C, 65°C, 66°C and 67°C, preferably of between 62°C to 66°C, and most preferablybetween 64°C to 65°C. Primer P2 preferably comprises or consists of a nucleic acid sequence of SEQ ID NOs: 50 to52. More preferably, primer P1 comprises or consists of a nucleic acid sequence according to SEQ IDNO: 50. Most preferably, P1 consists of the nucleic acid sequence according to SEQ ID NO: 50.Preferred characteristics of the primers P3 and P4 to be used in the context of the invention are disclosed in the following. Primer P3 preferably has a length of between 20 and 25 nucleotides, such as 20, 21, 22, 23, 24and 25 nucleotides, preferably between 21 and 24, 22 and 23, and most preferably a length of 23nucleotides. Primer P3 preferably has a melting temperature (Tm) of between 60°C and 70°C, such as60°C, 61°C, 62°C, 63°C, 64°C, 65°C, 66°C, 67°C, 68°C, 69°C and 70°C, preferably between 63°Cand 69°C, more preferably between 66°C to 68°C, and most preferably of 67°C. Primer P3 preferably comprises or consists of a nucleic acid sequence of SEQ ID NOs: 104.Most preferably, P3 consists of the nucleic acid sequence according to SEQ ID NO: 104.Primer P4 preferably has a length of between 15 and 21 nucleotides, such as 15, 16, 17, 18,19, 20, and 21 nucleotides, preferably between 16 and 20 nucleotides, or 17 and 19 nucleotides, andmost preferably a length of 17 nucleotides.Primer P4 preferably has a Tm of between of between 60°C to 67°C, such as 60°C, 61°C,62°C, 63°C, 64°C, 65°C, 66°C and 67°C, preferably of between 62°C to 66°C, and most preferablybetween 64°C to 65°C. Primer P4 preferably comprises or consists of a nucleic acid sequence of SEQ ID NOs: 105.Most preferably, P4 consists of the nucleic acid sequence according to SEQ ID NO: 105. The Tm of primers and in particular of primers P1 and P2 or of primers P3 and P4 ispreferably calculated using a software and the settings as described in the section ‘Definitions’ above.The method of the present invention comprises performing PCR on a sample suspected ofcomprising mycoplasma DNA and / or virus DNA such as MMV DNA with a PCR reaction mixturecomprising. The type of PCR is preferably real-time quantitative PCR (qPCR) or digital PCR (dPCR).The dPCR can be for example droplet digital PCR (ddPCR) or chip digital PCR (cdPCR). Aparticularly preferred PCR method according to the present invention is qPCR. The PCR is preferably performed by using an annealing temperature of between 55°C to 65°C for P1 and P2, such as 55°C, 56°C, 57°C, 58°C, 59°C, 60°C, 61°C, 62°C, 63°C, 64°C and 65°C,preferably between 58°C and 60°C. It is preferred that the annealing temperature of P1 and P2 or P3and P4 is about the same, such as within the range of about 2°C to 3°C difference between both primers, more preferably within the range of ± 1°C. For example, if P1 has an annealing temperature of about 59°C, it is preferred that P2 has an annealing temperature of 59°C ± 1°C. Although it is preferred that the annealing temperature of P1 and P2 or P3 and P4 is about the same, and more preferably identical, this is not mandatory. The elongation temperature can be readily selected by the person of ordinary skill in the art and may depend on the specific type of polymerase used in the reaction and the length of the expected PCR product to be generated in the reaction. Typical elongation temperatures are between 60°C and 80°C, typically at around 72°C, but may depend on the type of enzyme used. According to a preferred embodiment of the present invention, the annealing step and the elongation step are performed at the same temperature, and may thus be performed in the same step. For example, the annealing and elongation may take place at a temperature of between about 57°C and65°C, such as at about 58°C, 59°C, 60°C, 61°C, 62°C, 63°C, 64°C or 65°C. According to aparticularly preferred embodiment, the annealing and elongation may take place at a temperature of about 60°C. Such combined annealing and elongation steps are also simply referred to as amplificationstep and may speed up the time required for running the PCR. The duration of the amplification stepdepends on the size of the target to be amplified and the DNA polymerase used. For example, the amplification may require between about 20 and 60 seconds, between about 30 and 50 seconds or around 40 seconds. According to a preferred embodiment of the present invention, the duration of theamplification, i.e. the annealing and the elongation, takes about 30 seconds.A typical number of cycles comprising denaturation, annealing and elongation is between about 20 and 50 cycles, such as 20, 25, 30, 35, 40, 45 and 50 cycles, preferably between about 30 and 45 cycles. According to a particularly preferred embodiment, the PCR is run for about 45 cycles. The PCR may comprise in addition to the standard procedure of multiple cycles ofdenaturation, annealing and elongation, one or more additional steps preferably preceding said cyclesfor degrading contaminant DNA, such as contaminant DNA from remnant PCR products. Such adegradation is preferably performed by adding an enzyme such as uracil-DNA glycosylase (UNGase, e.g. from ArcticZymes Technologies, Norway) to the reaction mixture and applying a degradation step at about 40°C for a time period of between 60 and 180 seconds, preferably for 120 seconds. The temperature and duration of such an additional step may depend on the enzyme and its concentration used in the reaction mixture for degrading contaminant DNA, and may be readily selected by the person of ordinary skill in the art or by following the instructions of the manufacturer of the enzyme(s) used for this purpose. The PCR may, in addition to or as alternative to the degrading step, comprise a step ofactivating the reaction before the actual cycles are started. Such a starting or initiation step maycomprise applying a temperature of between about 88°C and 98°C, preferably of about 90°C, for about45 seconds to 10 minutes, preferably for about 60 seconds, to the reaction mixture comprising thesample and primers. The specific parameters of such an activation step may be readily selected by theperson of ordinary skill in the art or by following the instructions of the manufacturer of the polymerase or of any of the other reaction mixture components used in the PCR. A particularly preferred PCR protocol for the method of the present invention is disclosed in the following: Step Temperature Time Cycle(s)Enzym. degradation 40°C 120s 1Activation 90°C 60s 1Denaturation 90°CAmplification 60°C The detection of the PCR product may be performed by any respective method known in the field. For example, the PCR product generated may be detected during the PCR (also referred to as real time techniques) or after the PCR (also referred to as end point techniques). Real time techniques are performed inside the PCR reaction vessel and during PCR thermocycling using for example DNA binding fluorescent dyes (e.g. non-specific fluorescent dyes that intercalate with any double-stranded DNA), DNA hybridization (e.g. sequence-specific DNA probes consisting of oligonucleotides that are labelled e.g. with a fluorescent dye), or dNTP nucleotides with fluorescent dyes. End point techniques include but are not limited to DNA gel electrophoresis and the use of DNA intercalating dyes. Aparticularly preferred detection method is the use of sequence-specific DNA probes comprising a labeldirectly in the reaction mixture and thus during the PCR.In accordance with such a particularly preferred embodiment of the present invention, thereaction mixture for detecting mycoplasma may further comprise at least a first nucleic acid probe(herein referred to as Probe 1) in the reaction mixture. Probe 1 anneals to a nucleic acid sequence atleast 90% identical to SEQ ID NO: 53, or to the reverse complement of a nucleic acid sequence atleast 90% identical to SEQ ID NO: 53. Accordingly, the reaction mixture for detecting MMV mayfurther comprise at least a one nucleic acid probe (herein referred to as Probe 5) in the reactionmixture. Probe 5 anneals to a nucleic acid sequence at least 90% identical to SEQ ID NO: 111, or tothe reverse complement of a nucleic acid sequence at least 90% identical to SEQ ID NO: 111. According to a further particularly preferred embodiment of the present invention referring tothe detection of mycoplasma, the reaction mixture comprises a second nucleic acid probe (Probe 2),which anneals to a nucleic acid sequence at least 90% identical to SEQ ID NO: 53, or to the reversecomplement of a nucleic acid sequence at least 90% identical to SEQ ID NO: 53. Probe 2 anneals orbinds to a different section on the nucleic acid sequence at least 90% identical to SEQ ID NO: 53 or tothe reverse complement thereof than Probe 1. Preferably, Probe 2 anneals to a section on the nucleicacid sequence at least 90% identical to SEQ ID NO: 53 or to the reverse complement thereof separatedby at least two nucleotides from the section on the nucleic acid sequence at least 90% identical to SEQID NO: 53 or to the reverse complement thereof to which Probe 1 anneals or binds.Probe 1 and / or Probe 2 or Probe 5 may be present in a pre-mix of the reaction mixture or may be added before the PCR is started. Preferred characteristics of Probe 1, Probe 2 and Probe 5 are disclosed in the following.Probe 1 and / or Probe 2 preferably have a length between about 20 and 42 nucleotides, such asabout 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41 and 42nucleotides, more preferably of between about 21 and 30 nucleotides, and most preferably of betweenabout 22 and 24 nucleotides. The most preferred length of Probe 1 and / or Probe 2 is 23 nucleotides.Probe 5 preferably has a length between about 15 and 30 nucleotides, such as about 15, 16, 17, 18, 19,20, 21, 22, 23, 24, 25, 26, 27, 28, 29, and 30 nucleotides, more preferably of between about 18 and 22nucleotides, and most preferably of between about 19 and 21 nucleotides. The most preferred length ofProbe 5 is 20 nucleotides.Probe 1 and / or Probe 2 preferably have a Tm of between about 55°C and 70°C, such as about55°C, 56°C, 57°C, 58°C, 59°C, 60°C, 61°C, 62°C, 63°C, 64°C, 65°C, 66°C, 67°C, 68°C, 69°C and70°C, more preferably of about between 58°C and 69°C, and most preferably of about between 59°Cand 68°C, such as between about 59°C and 67°C, between about 59°C and 66°C, between about 59°Cand 65°C, between about 59°C and 64°C, between about 59°C and 63°C, between about 59°C and 62°C, between about 59°C and 61°C. Probe 5 preferably has a Tm of between about 59°C and 71°C, such as about 59°C, 60°C,61°C, 62°C, 63°C, 64°C, 65°C, 66°C, 67°C, 68°C, 69°C, 70°C, and 71°C, more preferably of aboutbetween 60°C and 70°C, and most preferably of about between 62°C and 68°C, such as between about63°C and 67°C, between about 64°C and 66°C. Probe 1 preferably comprises or consists of a nucleic acid sequence of SEQ ID NOs: 54 to 65.More preferably, Probe 1 comprises or consists of a nucleic acid sequence according to SEQ ID NO:62, most preferably Probe 1 consists of a nucleic acid sequence according to SEQ ID NO: 62. Probe 1may comprise one or more locked nucleic acids (LNA). In addition to or as an alternative to LNAs,Probe 1 may comprise one or more of a minor grove binding (MGB) moiety. According to oneparticularly preferred embodiment, Probe 1 consists of a nucleic acid sequence according to SEQ IDNO: 62 and comprises LNAs, preferably five LNAs as shown in SEQ ID NO: 60 (underlined nucleotides represent LNA modifications). Probe 2 preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 66. Morepreferably, Probe 2 consists of a nucleic acid sequence according to SEQ ID NO: 66. Probe 2 maycomprise one or more LNAs. In addition or as an alternative to LNAs, Probe 2 may comprise one or more of a minor grove binding (MGB) moiety. According to one particularly preferred embodiment,Probe 2 consists of a nucleic acid sequence according to SEQ ID NO: 66 and comprises LNAs,preferably three LNAs as shown in SEQ ID NO: 67 (underlined nucleotides represent LNAmodifications). Probe 5 preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 106. Morepreferably, Probe 5 consists of a nucleic acid sequence according to SEQ ID NO: 106. Probe 5 maycomprise one or more locked nucleic acids (LNA). In addition to or as an alternative to LNAs, Probe 5 may comprise one or more of a minor grove binding (MGB) moiety. If the length of Probe 1 and / or Probe 2 exceeds about 30 nucleotides, internal quenchers can be used instead of the LNA and / or MEG modifications. Internal quenchers can be for example ZEN and / or TAO modifications. Such internal quenchers are particularly useful in long probes comprising afluorescent dye at one end and a quencher at the other end, in order to increase assay efficiency bydecreasing the number of cycles required to meet the signal threshold compared to single-quenchedprobes, and by providing greater overall dye quenching, thus resulting in decreased backgroundfluorescence and improved signal to noise ratio. Probe 1 and / or Probe 2 and / or Probe 5 comprise one or more detectable labels. According to one embodiment, Probe 1 and Probe 2 comprise the same detectable label(s). The detectable label can be any label that allows identification of the probes. A preferred detectable label is a fluorescent dye.Preferred fluorescent dyes include but are not limited to FAM, HEX, NED, TET, VIC, Cy3, Cy5,Texas Red or Tide Fluor™ dyes, more preferably FAM. The fluorescent dye is preferably attached tothe 5’ end of the nucleic acid probe. In such a case, the probe may further comprise a quencher dye attached to its 3’ end. Preferred quencher dyes include but are not limited to DABCYL, TAMRA,BXQ-1, BXQ-2, IABkFQ, IABkRQ or Tide Quencher™ dyes, more preferably IABkFQ. IABkFQ andIABkRQ are Iowa Black® FQ and RQ, respectively, obtainable from Integrated DNA Technologies,Inc., USA. IABkFQ is preferably used in combination with FAM, HEX, NED, TET and VIC, andIABkRQ is preferably used in combination with Cy5 or Texas Red. Probe 1 and / or Probe 2 and / orProbe 5 are preferably hydrolysis probes comprising a fluorescent dye at their 5’ end and a quencherdye at their 3’ end. A particularly preferred combination for Probe 1, Probe 2 and Probe 5 is FAM / IABkFQ. While the hydrolysis probe is intact, the fluorescent dye and quencher dye remain in close proximity to each other, FRET occurs, and fluorescent dye is quenched. When during PCR cycling, the DNA polymerase binds to and extends the primer upstream of the probe, any probe bound to the correct target sequence is hydrolyzed. The fluorescent dye fragment is released, resulting in a fluorescence signal proportional to the amount of amplicon produced, thus allowing detection of the PCR product during the reaction.

[0008] According to a particularly preferred embodiment, Probe 1 consists of SEQ ID NO: 60 and comprises the fluorochrome / quencher pair FAM / lABkFQ. According to a further particularly preferred embodiment, Probe 2 consists of SEQ ID NO: 67 and comprises the fluorochrome / quencher pair FAM / lABkFQ. According to a further particularly preferred embodiment, Probe 5 consists of SEQ ID NO: 106 and comprises the fluorochrome / quencher pair FAM / lABkFQ.

[0009] According to a particularly preferred embodiment of the present invention regarding the detection of mycoplasma, the reaction mixture comprises primer P 1 , primer P2, Probe 1 and Probe 2 as described herein.

[0010] According to a particularly preferred embodiment of the present invention regarding the detection of MMV, the reaction mixture comprises primer P3, primer P4, and Probe 5 as described herein.

[0011] According to one embodiment, in the method of the present invention, tire reaction mixture additionally comprises a positive control nucleic acid sequence, which is also referred to as internal positive control (IPC). The IPC may be present in a pre-mix of the reaction mixture or it may be added to the reaction mixture before the PCR is started.

[0012] In die embodiment for detecting mycoplasma, the positive control nucleic acid sequence or myco-IPC comprises at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1, at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2, and an intervening nucleic acid sequence of a length of at least 18 nucleotides between these two nucleic acid sequences. This intervening sequence of at least 18 nucleotides preferably differs from SEQ ID NO: 53 in such a way that neither Probe 1 (if present) nor Probe 2 (if present) anneals to the intervening nucleic acid sequence. According to a particularly preferred embodiment, a third probe (Probe 3) anneals or binds to said intervening sequence or to its reverse complement. The intervening nucleic acid sequence preferably has a length of about 20 to 150 nucleotides, about 30 to 140 nucleotides, or about 40 to 120 nucleotides, such as 50, 60, 70, 80, 90, 100, 110 or about 120 nucleotides. According to a particularly preferred embodiment, the intervening nucleic acid sequence has a length of about 120 nucleotides. hi the embodiment for detecting mycoplasma, the internal positive control nucleic acid sequence or myco-IPC preferably comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 68, or to the reverse complement of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 68. The myco-IPC is preferably in the form of a double-stranded DNA molecule, more preferably in the form of a gBlock. According to a particularly preferred embodiment, the myco-IPC is a gBlock comprising or consisting of SEQ ID NO: 68 and its reverse complement. For detecting the myco-IPC amplicons, Probe 3 can be used. Thus, according to one embodiment, the reaction mixture further comprises Probe 3, which may be present in a pre-mix of thereaction mixture or added before the PCR is started. Probe 3 preferably has one or more of thespecifics described above in the context of Probes 1 and 2 regarding their length, Tm and label, withthe proviso that the label for Probe 3 is different from the label selected for Probe 1 and Probe 2,allowing to distinguish Probe 3 from Probes 1 and 2. Probe 3 may also comprise one or more of anLNA and / or MGB modification. Probe 3 preferably has a length of between 20 and 42 nucleotides,more preferably of between 21 and 30 nucleotides, and most preferably of between 22 and 24nucleotides. According to one embodiment, Probe 3 has a Tm of between about 55°C and 70°C, preferably between about 58°C and 69°C, more preferably between about 59°C and 68°C, and mostpreferably of about 60°C. Probe 3 preferably comprises or consists of a nucleic acid sequence of SEQID NO: 69 or its reverse complement. More preferably, Probe 3 consists of a nucleic acid sequence ofSEQ ID NO: 69 or its reverse complement. According to a preferred embodiment, Probe 3 comprisesthe fluorochrome / quencher pair Cy5 / IABkRQ. According to a particularly preferred embodiment,Probe 3 consists of a nucleic acid sequence of SEQ ID NO: 69 and comprises thefluorochrome / quencher pair Cy5 / IABkRQ.If the myco-IPC is present during the PCR, Primers 1 and 2 also bind to the IPC and allowamplification thereof. The presence of IPC amplicons can be detected using for example Probe 3.Alternatively, the presence of IPC amplicons can be detected using the real time techniques or endpoint techniques described herein. If IPC amplification product is detected during and / or at the end ofthe PCR, the reaction parameters chosen were sufficient for enabling amplification of potential targets in a sample. If only myco-IPC amplicons are detected and no further PCR products, this means that the sample did not contain any mycoplasma. In the embodiment for detecting MMV, the positive control nucleic acid sequence or mmv-IPC comprises at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 109,at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 110, and anintervening nucleic acid sequence of a length of at least 18 nucleotides between these two nucleic acidsequences. This intervening sequence preferably does not allow binding of Probe 3 (if present) orProbe 5 (if present) to the intervening nucleic acid sequence. According to a particularly preferredembodiment, Probe 4 anneals or binds to said intervening sequence or to its reverse complement. Theintervening nucleic acid sequence preferably has a length of about 20 to 150 nucleotides, about 30 to140 nucleotides, or about 40 to 120 nucleotides, such as 50, 60, 70, 80, 90, 100, 110 or about 120nucleotides. According to a particularly preferred embodiment, the intervening nucleic acid sequence has a length of about 120 nucleotides. In the embodiment for detecting MMV, the internal positive control nucleic acid sequence or mmv-IPC preferably comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 112 or 116 or to the reverse complement of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 112 or 116. According to an alternative embodiment, the mmv-IPC comprises or consists of a nucleic acid sequence at least90% identical to the nucleic acid sequence of 68 or 112 or 115, or to the reverse complement of anucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 68 or 112 or115. The myco-IPC is preferably in the form of a double-stranded DNA molecule, more preferably in the form of a gBlock. According to a particularly preferred embodiment, the myco-IPC is a gBlock comprising or consisting of SEQ ID NO: 68 and its reverse complement. For detecting the mmv-IPC amplicons, Probe 4 can be used. Thus, according to oneembodiment, the reaction mixture further comprises Probe 4, which may be present in a pre-mix of thereaction mixture or added before the PCR is started. Probe 4 as described herein above. Probe 4 mayalso comprise one or more of an LNA and / or MGB modification. Probe 4 preferably has a length ofbetween 20 and 42 nucleotides, more preferably of between 21 and 30 nucleotides, and mostpreferably of between 22 and 24 nucleotides. According to one embodiment, Probe 4 has a Tm ofbetween about 55°C and 70°C, preferably between about 58°C and 69°C, more preferably betweenabout 59°C and 68°C, and most preferably of about 60°C. Probe 4 preferably comprises or consists ofa nucleic acid sequence of SEQ ID NO: 69 or its reverse complement. More preferably, Probe 4consists of a nucleic acid sequence of SEQ ID NO: 69 or its reverse complement. According to apreferred embodiment, Probe 4 comprises the fluorochrome / quencher pair Cy5 / IABkRQ. Accordingto a particularly preferred embodiment, Probe 4 consists of a nucleic acid sequence of SEQ ID NO: 69and comprises the fluorochrome / quencher pair Cy5 / IABkRQ.If the mmv-IPC is present during the PCR, Primers 3 and 4 also bind to the IPC and allowamplification thereof. The presence of IPC amplicons can be detected using for example Probe 4. Alternatively, the presence of IPC amplicons can be detected using the real time techniques or endpoint techniques described herein. If IPC amplification product is detected during and / or at the end ofthe PCR, the reaction parameters chosen were sufficient for enabling amplification of potential targets in a sample. If only mmv-IPC amplicons are detected and no further PCR products, this means that the sample did not contain any mouse minute virus. According to one embodiment, in the method of the present invention, the reaction mixture orthe sample additionally comprises a discriminatory positive control nucleic acid sequence, which isalso referred to as DPC. Alternatively, the DPC can be used in a separate control reaction using the same parameters as the PCR for mycoplasma or MMV detection but comprising the DPC instead of the sample. In the embodiment for detecting mycoplasma, the discriminatory positive control nucleic acidsequence or myco-DPC comprises at least 18 consecutive nucleic acids of the nucleic acid sequence ofSEQ ID NO: 1, at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2,and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of atleast 18 nucleotides. This intervening sequence of at least 18 nucleotides preferably does not differfrom but rather comprises SEQ ID NO: 53 or a part therefrom. The length of the intervening nucleicacid sequence preferably allows annealing or binding of Probe 1 (if present) and preferably Probe 2 (ifpresent). According to a preferred embodiment, the intervening sequence has a length allowingbinding or annealing of a fourth probe (Probe 4). Thus, the intervening sequence of the DPCpreferably has a length of between 18 and about 200 nucleotides, such as between about 25 and 190, between about 30 and 180, between about 35 and 170, between about 40 and 160, between about 50 and 150, between about 60 and 140, between about 70 and 130, between about 80 and 120, or betweenabout 90 and 110 nucleotides. Preferably, the sequence of the intervening nucleic acid sequence or toits reverse complement to which Probe 4 anneals to or binds to is different from the sequence of theintervening nucleic acid sequence to which Probe 1 and / or Probe 2 anneals or binds to.In the embodiment for detecting mycoplasma, the discriminatory positive control nucleic acid sequence or myco-DPC preferably comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 70, or to the reverse complement of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 70. The myco-DPC is preferably in the form of a double-stranded DNA molecule, more preferably in the form of a gBlock. According to a particularly preferred embodiment, the myco-DPC is a gBlock comprising or consisting of SEQ ID NO: 70 and its reverse complement. In the embodiment for detecting mycoplasma, for detecting the myco-DPC, a further Probe 4 can be used. Probe 4 preferably binds or anneals to the myco-DPC in a region distinct from the region to which Probe 1 (if present) and Probe 2 (if present) bind or anneal to. Probe 4 preferably has one or more of the specifics described above in the context of Probes 1 and 2 regarding their length, Tm and label, with the proviso that the label for Probe 4 is different from the label selected for Probe 1, Probe 2 and Probe 3, allowing to distinguish Probe 4 from the other probes. Probe 4 may also comprise one or more of an LNA and / or MGB modification. According to one embodiment, Probe 4 has a length of between 20 and 42 nucleotides, preferably of between 21 and 30 nucleotides, and most preferably of between 22 and 24 nucleotides. According to a preferred embodiment, Probe 4 has a Tm of between about 55°C and 70°C, preferably of between about 58°C and 69°C, more preferably of between about 59°C and 68°C, and most preferably of about 60°C. Probe 4 preferably comprises or consists of anucleic acid sequence of SEQ ID NO: 71 or its reverse complement. More preferably, Probe 4 consistsof a nucleic acid sequence of SEQ ID NO: 71 or its reverse complement. According to a preferredembodiment, Probe 4 comprises the fluorochrome / quencher pair HEX / IABkFQ. According to aparticularly preferred embodiment, Probe 4 consists of a nucleic acid sequence of SEQ ID NO: 71 andcomprises the fluorochrome / quencher pair HEX / IABkFQ. According to one embodiment, the reactionmixture further comprises the myco-DPC and Probe 4, both of which may be present in a pre-mix of the reaction mixture or added before the PCR is started. Alternatively, if the myco-DPC is used in a separate control reaction, the separate control reaction uses the same parameters as the PCR for mycoplasma detection but comprises the myco-DPC instead of the sample, and Probe 4. A particularly preferred combination of primers and probes to be used in the method of theinvention for detecting mycoplasma comprises primer P1 consisting of the nucleic acid sequence ofSEQ ID NO: 9, primer P2 consisting of the nucleic acid sequence of SEQ ID NO: 50, a first probe (Probe 1) consisting of the nucleic acid sequence of SEQ ID NO: 60, and a second probe (Probe 2) consisting of the nucleic acid sequence of SEQ ID NO: 67. In this particularly preferred combination of primers and probes for detecting mycoplasma in a sample, Probe 1 preferably comprises thefluorochrome / quencher pair FAM / IABkFQ, and Probe 2 preferably comprises thefluorochrome / quencher pair FAM / IABkFQ. In the embodiment for detecting MMV, the discriminatory positive control nucleic acid sequence or mmv-DPC comprises at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 109, at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 110, and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides. The intervening nucleic acid sequence preferably allows annealing or bindingof Probe 5 (if present) and preferably Probe 3 (if present). Thus, the intervening sequence of the mmv-DPC preferably has a length of between 18 and about 200 nucleotides, such as between about 25 and 190, between about 30 and 180, between about 35 and 170, between about 40 and 160, between about 50 and 150, between about 60 and 140, between about 70 and 130, between about 80 and 120, orbetween about 90 and 110 nucleotides. According to a preferred embodiment, the intervening nucleicacid sequence of the mmv-DPC has a length of at least 29 nucleotides. According to a particularlypreferred embodiment, the intervening nucleic acid sequence of the mmv-DPC does not differ fromSEQ ID NO: 111 so that Probe 5 is capable of annealing to said intervening nucleic acid sequence.In the embodiment for detecting MMV, the discriminatory positive control nucleic acid sequence or mmv-DPC preferably comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 113, or to the reverse complement of a nucleicacid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 113. According toone embodiment, the mmv-DPC comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 114, or to the reverse complement of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 114. The mmv-DPC is preferably in the form of a double-stranded DNA molecule, more preferably in the form of a gBlock. According to a particularly preferred embodiment, the mmv-DPC is a gBlock comprising orconsisting of SEQ ID NO: 114 and its reverse complement.In the embodiment for detecting MMV, Probe 5 preferably binds or anneals to the mmv-DPCin a region distinct from the region to which Probe 3 binds or anneals to. Probe 5 preferably has one ormore of the specifics described herein above e.g. regarding its length, Tm and label, with the provisothat the label for Probe 5 is different from the label selected for Probe 3 and / or Probe 4, allowing todistinguish Probe 5 from the other probes. The concentrations of the individual components in the reaction mixture can be readily selected by the skilled person. According to a particularly preferred embodiment, preferably in combination with the particularly preferred combination of primers and probes described herein above, the PCR reaction mixture comprises primers such as P1 and P2 or P3 and P4 in a concentration of about 400 nM; and Probe 1 and Probe 2 or Probe 5 in a concentration of about 200 nM. In embodiments comprising the internal positive control (IPC), the PCR reaction mixture preferably further comprises the control such as Probe 3 and optionally Probe 4 in a concentration of about 200 nM. The IPC is preferably present in an amount of about 200 copies in the PCR reaction mixture. It is to be noted that the indicated concentrations refer to the respective concentrations in the final PCR reaction mixture used in the actual reaction. The skilled person readily understands that master mixesor pre-mixes of the reaction mixture or parts thereof can be prepared, in which the concentrationsdeviate from the above cited final concentrations. Such master mixes or pre-mixes are commonlydiluted with H2O and / or buffer solutions, giving rise to the final reaction mixture. According to a preferred embodiment, the reaction mixture further comprises an enzyme for degrading unwanted DNA such as remnant and / or contaminating DNA. A preferred enzyme for degradation is UNGase. Thus, according to a particularly preferred embodiment, the reaction mixturein addition to the particularly preferred combination of primers, probes and IPC described hereinabove comprises UNGase, preferably in a final concentration of 1U per 100 μL of reaction mixture.A most preferred combination of primers, probes and other components for the polymerasechain reaction is set forth in the following table 3.Table 3.1: preferred concentrations in reaction mixture for mycoplasma detectionComponent [C]finalqPCR Master Mix 1x UNGase 1 u / 100µLPrimer 1 400 / 800 nMPrimer 2 400 / 800 nMProbe 1 200 nMProbe 2 200 nMoptionally Probe 3 200 nMoptionally Probe 4 200 nMoptionally myco-IPC gBlock 200 cpTable 3.2: preferred concentrations in reaction mixture for MMV detectionComponent [C]finalqPCR Master Mix 1xComponent [C]finalUNGase 1 u / 100µLPrimer 1 400 / 800 nMPrimer 2 400 / 800 nMProbe 5 200 nMoptionally Probe 3 200 nMoptionally mmv-IPC gBlock 200 cpThe primer concentration for mycoplasma detection or for MMV detection may be either400 nm for both primers or alternatively 800 nm for both primers. According to a particularly preferred embodiment of the present invention relating to thedetection of mycoplasma, the concentration of primers and probes is as set forth in the above table 3.1,with Primer 1 being Fw Myco7, Primer 2 being Rev Myco1*, Probe 1 being Myco5 bis, Probe 2 being Acho1, Probe 3 (if present) being SAtPSY, Probe 4 (if present) being StraA, and IPC gBlock (if present) comprising SEQ ID NO: 68. Thus, according to a particularly preferred embodiment, thepresent invention comprises the combination set forth in the following table 4.1.Table 4.1: Preferred components and their preferred concentrations for mycoplasma detectionComponent [C]finalqPCR Master Mix (e.g. Luna Universal Probe) 1xUNGase 1 u / 100µLPrimer 1 (Fw Myco7) 400 nMPrimer 2 (Rev Myco1*) 400 nMProbe 1 (Myco5 bis) 200 nMProbe 2 (Acho1) 200 nMoptionally Probe 3 (SAtPSY) 200 nMoptionally Probe 4 (StraA) 200 nMoptionally IPC gBlock (SEQ ID NO: 68) 200 cpAccording to a particularly preferred embodiment of the present invention relating to the detection of MMV, the concentration of primers and probes is as set forth in the above table 3.2, with Primer 3 being Fw MMV, Primer 4 being Rev MMV, Probe 5 being Probe MMV, Probe 3 (if present) being SAtPSY, Probe 4 (if present) being StraA, and IPC gBlock (if present) comprising SEQ ID NO: 68. Thus, according to a particularly preferred embodiment, the present invention comprises the combination set forth in the following table 4.2.Table 4.2: Preferred components and their preferred concentrations for MMV detectionComponent [C]finalqPCR Master Mix (e.g. Luna Universal Probe) 1xUNGase 1 u / 100µLPrimer 3 (Fw MMV) 800 nMPrimer 4 (Rev MMV) 800 nMProbe 5 (Myco5 bis) 200 nMoptionally Probe 3 (SAtPSY) 200 nMoptionally Probe 4 (StraA) 200 nMoptionally IPC gBlock (SEQ ID NO: 68) 200 cpIn accordance with a particularly preferred embodiment for detecting MMV, the reaction mixture comprises the following: Primer 3 having SEQ ID NO: 104, Primer 4 having SEQ ID NO:105, Probe 5 having SEQ ID NO: 106 and comprising the fluorochrome / quencher pair FAM / IABkFQ, and mmv-IPC having SEQ ID NO: 68. This reaction mixture preferably further comprises Probe 4 having SEQ ID NO: 71 and comprising the fluorochrome / quencher pair HEX / IABkFQ. This reaction mixture optionally further comprises mmv-DPC comprising SEQ ID NO: 113 and preferablyProbe 3 having SEQ ID NO: 69 and comprising the fluorochrome / quencher pair Cy5 / IABkRQ.It will be appreciated that IPC and DPC can be present in the same reaction mixture as the PCR reaction mixture comprising Primers 1 and 2 or 3 and 4. Alternatively, IPC and DPC can be present combined in a separate reaction mixture or separated in separate reaction mixtures. The present invention further provides a pair of primers comprising a primer P1 annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 1, and a primer P2 annealing to anucleic acid sequence of SEQ ID NO: 2. These primers can be used for detecting mycoplasma in asample, and in particular in respective PCR assays for detecting mycoplasma as described herein. According to one embodiment, primer P1 and primer P2 have one or more of the characteristicsdescribed for P1 and P2 above. P1 preferably comprises or consists of a nucleic acid sequence of anyone of SEQ ID NOs: 3 to 49. More preferably, primer P1 comprises or consists of a nucleic acidsequence according to SEQ ID NO: 9. Most preferably, P1 consists of the nucleic acid sequenceaccording to SEQ ID NO: 9. Primer P2 preferably comprises or consists of a nucleic acid sequence ofany one of SEQ ID NOs: 50 to 52. More preferably, primer P2 comprises or consists of a nucleic acidsequence according to SEQ ID NO: 50. Most preferably, P2 consists of the nucleic acid sequenceaccording to SEQ ID NO: 50. Aparticularly preferred primer pair according to the present invention comprises primer P1consisting of SEQ ID NO: 9, and primer P2 consisting of SEQ ID NO: 50.The present invention also provides a pair of primers comprising a primer P3 annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 109, and a primer P4 annealing to a nucleic acid sequence of SEQ ID NO: 110. These primers can be used for detecting MMV in a sample, and in particular in respective PCR assays for detecting virus and in particular MMV as described herein. According to one embodiment, primer P3 and primer P4 have one or more of the characteristics described for P3 and P4 above. P3 preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 104. More preferably, P3 consists of the nucleic acid sequence according to SEQ ID NO: 104. Primer P4 preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 105. More preferably, primer P4 consists of the nucleic acid sequence according to SEQ ID NO: 105.

[0013] The present invention further provides a kit for detecting mycoplasma in a sample. The kit comprises the pair of primers of the present invention as described herein above, and a first nucleic acid probe (Probe 1) annealing to or binding to a nucleic acid sequence of SEQ ID NO: 53 or to its reverse complement. According to one embodiment, the kit further comprises a second nucleic acid probe (Probe 2) annealing to or binding to SEQ ID NO: 53 or to its reverse complement. Probe 1 and / or Probe 2 preferably have one or more of the characteristics of Probe 1 and Probe 2, respectively, as described herein above. Probe 1 preferably comprises or consists of a nucleic acid sequence of SEQ ID NOs: 54 to 65. More preferably, Probe 1 comprises or consists of a nucleic acid sequence according to SEQ ID NO: 62, most preferably Probe 1 consists of anucleic acid sequence according to SEQ ID NO: 62. Probe 1 may comprise one or more locked nucleic acids (ENA). In addition or as an alternative to LNAs, Probe 1 may comprise one or more of a minor grove binding (MGB) moiety. According to one particularly preferred embodiment, Probe 1 consists of a nucleic acid sequence according to SEQ ID NO: 62 and comprises LNAs, preferably five LNAs as shown in SEQ ID NO: 60 (underlined nucleotides represent ENA modifications). Probe 2, if present, preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 66. More preferably, Probe 2 consists of a nucleic acid sequence according to SEQ ID NO: 66. Probe 2 may comprise one or more LNAs. In addition or as an alternative to LNAs, Probe 2 may comprise one or more of a minor grove binding (MGB) moiety. According to one particularly preferred embodiment, Probe 2 consists of a nucleic acid sequence according to SEQ ID NO: 66 and comprises LNAs, preferably three LNAs as shown in SEQ ID NO: 67 (underlined nucleotides represent LNA modifications).

[0014] According to a particularly preferred embodiment, the kit comprises primer Pl, primer P2, Probe 1 and Probe 2 as described herein, more preferably primer Pl consisting of the nucleic acid sequence of SEQ ID NO: 9, primer P2 consisting of the nucleic acid sequence of SEQ ID NO: 50, Probe 1 consisting of the nucleic acid sequence of SEQ ID NO: 60, and Probe 2 consisting of the nucleic acid sequence of SEQ ID NO: 67. In this particularly preferred combination of primers and probes of the kit, Probe 1 preferably comprises the fluorochrome / quencher pair FAM / lABkFQ, and Probe 2 preferably comprises the fluorochrome / quencher pair FAM / lABkFQ.

[0015] The kit may further comprise one or more of a PCR reaction mixture as described herein above, an internal positive control nucleic acid sequence (IPC) as described herein above, a discriminatory positive control nucleic acid sequence (DPC) as described herein above, means forextracting and / or purifying DNA from the sample as described herein above, and instructions forperforming PCR with the primers. If an IPC and / or a DPC is part of the kit of the invention, the kit preferably further comprises a Probe 3 and Probe 4, respectively, as described herein, for aligning to or binding to the IPC and DPC, respectively. Using the present invention, that is the method of the invention, the set of primers of the present invention, or the kit of the present invention, it is possible to detect mycoplasma in a sample. The mycoplasma that can be detected is preferably one or more of the Mycoplasma species Mycoplasma arginini, Mycoplasma buccale, Mycoplasma hominis, Mycoplasma orale, Mycoplasma salivarium, Mycoplasma fermentans, Mycoplasma hyorhinis, Mycoplasma synoviae, Mycoplasmapneumoniae, Acholeplasma laidlawii, Mycoplasma gallisepticum and Spiroplasma citri.The present invention further provides a kit for detecting MMV in a sample. The kit comprisesthe pair of primers of the invention as described herein above, and a nucleic acid probe (Probe 5)annealing to a nucleic acid sequence of SEQ ID NO: 111 or its reverse complement.Probe 5 preferably has one or more of the characteristics of Probe 5 as described herein above. Probe 5 preferably comprises or consists of a nucleic acid sequence of SEQ ID NO: 106. Probe 5 may comprise one or more locked nucleic acids (LNA). In addition or as an alternative to LNAs, Probe 5 may comprise one or more of a minor grove binding (MGB) moiety. According to one particularlypreferred embodiment, Probe 5 consists of a nucleic acid sequence according to SEQ ID NO: 106 andcomprises LNAs. In addition or as an alternative to LNAs, Probe 5 may comprise one or more of aminor grove binding (MGB) moiety. According to a particularly preferred embodiment, the kit comprises primer P3, primer P4, and Probe 5 as described herein, more preferably primer P3 consisting of the nucleic acid sequence of SEQID NO: 104, primer P4 consisting of the nucleic acid sequence of SEQ ID NO: 105, and Probe 5consisting of the nucleic acid sequence of SEQ ID NO: 106, In this particularly preferred Ccombination of primers and probes of the kit, Probe 5 preferably comprises the fluorochrome / quencher pair FAM / IABkFQ. According to one embodiment, the kit further comprises one or more of a PCR reaction mixture as described herein above, an internal positive control nucleic acid sequence as described herein above, a discriminatory positive control nucleic acid sequence as described herein above,means for extracting and / or purifying DNA from the sample as described herein above, andinstructions for performing PCR with the primers. If an IPC and / or a DPC (such as mmv-IPC and / ormmv-DPC as described herein above) is part of the kit of the invention, the kit preferably furthercomprises Probe 5, Probe 3 and / or Probe 4 as described herein.According to one embodiment, in the method according to the invention, in the pair of primersaccording to the invention or in the kit according to the invention, the virus is selected from the groupconsisting of Anelloviridae, Inoviridae, Parvoviridae, preferably Parvovirus, Erythovirus, Dependovirus, Amdovirus and Bocavirus, more preferably Parvovirus, and most preferably Mouse Minute Virus. Also disclosed herein is a combination of the set of primers or the kit for detecting mycoplasma and of the set of primers or the kit for detecting virus. In other words, the presentinvention also provides a method, primers and a kit for the detection of mycoplasma and virus in asample. According to one embodiment, the detection of mycoplasma and virus is performedsimultaneously, preferably in the same reaction vessel such as a PCR tube. According to an alternative embodiment, the detection of mycoplasma and virus is performed subsequently, preferably in different reaction vessels such as a PCR tubes. Examples Materials and Methods All sequences referred to herein were retrieved from SILVA and NCBI websites (www.arb- silva.de and www.ncbi.nlm.nih.gov). Sequence analysis was performed with Vector NTI, Snap Gene and Geneious softwares. For primer thermodynamics calculation (Tm, primer dimer formation andhairpin Tm), PrimerExpress® 3.0 (Life Technologies Corporation), Geneious (Geneious Prime 2023.2;Dotmatics) and the IDT (Integrated DNA Technologies, Inc., USA) online software were used. Settings were as follows• PrimerExpress: standard settings• Geneious: Monovalent ions 50 mM; Divalent ions 3 mM; Primer 200 nM; dNTP 0.8 mM• IDT: Parameter set, qPCR; Monovalent ions 50 mM; Divalent ions 3 mM; Primer 200 nM;dNTP 0.8 mM.Similar parameters were used for probe thermodynamics calculation.Example 1: Identification of regions for primer designOrganisms used for the identification of regions for primer design are listed in following Table5. These include the Mycoplasma species and other germs which presence should be investigated in various cell substrates taken from the production workflow (Master Cell Bank, Working Cell Bank, Unprocessed Bulk, End Of Production Cells) as indicated in various guidelines. Table 5: Organisms used in the identification of regions for primer designOrganism Strain ATCC NCTC GenbankTotal length Accession No. (base pairs)Acholeplasma laidlawii* PG-8A ATCC 23206 NCTC10116 NZ_LS483439.1 1514Mycoplasma arginini* G230 ATCC 23838 NCTC10129 NZ_LR215044.1 1525Mycoplasma buccale CH20247 ATCC 23636 NTCC10136 AF_125586.1 1463Mycoplasma fermentans* PG18 ATCC 19989 NCTC10117 LR_214962.1 1502Mycoplasma gallisepticum* PG31 ATCC 19610 NCTC10115 NZ_LS991952.1 1520Mycoplasma hominis ATCC 23114 NCTC10111 NC_013511.1 1522Mycoplasma hyorhinis* BTS7 ATCC 17981 NZ_KB911485.1 1536Mycoplasma hyorhinis* ATCC 17981 NCTC10130 NZ_LS991950.1 1528Mycoplasma hyorhinis* DBS1050 ATCC 29052 NCTC10130 NC_022807.1 1528Mycoplasma orale* ATCC 23714 NCTC10112 NZ_LR214940.1 1522Mycoplasma pneumoniae* ATCC 15531 NCTC10119 NZ_LR214945.1 1520Mycoplasma salivarium ATCC 23064 NCTC10113 NZ_LR214938.1 1531Mycoplasma synoviae* ATCC 25204 NCTC10124 NZ_LS991953.1 1506Spiroplasma citri* R8-A2 ATCC 27556 NCTC10164 NZ_CP013197.1 1532Bacillus cereus ATCC 14579 NR_074540.1 1512Bacillus subtilis IAM 1211 ATCC 6051 NR_112116.2 1550Clostridium* perfringens ATCC 13124 NR_121697.2 1513Clostridium* sporogenes ATCC 15579 ABKW02000002 1500Escherichia coli A99 MK506978.1 1370Lactobacillus* acidophilus ATCC 4796 ACHN01000039.1 1552Lactobacillus* plantarum NRRL B-14768 NR_042394.1 1474Micrococcus luteus ATCC 4698 NR_114673.1 1325Staphylococcus aureus ATCC 12600 NR_118997.2 1552Staphylococcus saprophyticus ATCC 15305 NR_074999.2 1553Streptococcus* bovis ATCC 33317 AB002482.1 1457Streptococcus* pneumoniae ATCC 33400 MW407059.1 1515Homo sapiens EU545435.1 1558Cricetulus griseus CCL-14 DQ334846.1 1032Cricetulus griseus AY011148.1 808* Required by PhEu 2.6.7 In order to identify genomic regions to be targeted by PCR and to ensure specific mycoplasmadetection while excluding signals with other organisms, 16s and 23s ribosomal RNA sequences fromthe organisms listed in Table 5 were retrieved from SILVA and NCBI websites (www.arb-silva.de andwww.ncbi.nlm.nih.gov) and compared. Sequences from 23s rRNA were excluded for being too uniqueand thus not suitable for identifying essentially all mycoplasma species with only a limited number ofprimers and probes. On the other hand, 16s RNA displays some specificity but retains enoughhomology across mycoplasma species. It was therefore decided to focus on the 16s rRNA sequences toidentify regions that are common to all mycoplasma species which primer and probe sets shouldrecognize, and which are further significantly different from all other species. Using such sequencestretches ensures specific mycoplasma detection without cross reactions with DNA from other species.A first analysis focused on mycoplasma 16s rRNA sequences aimed at identifying 100 bpstretches with 80% homology across species, where primers and probes of 20 and 23 nucleotides,respectively, could be designed for mycoplasma detection by PCR. Domains with high homology to E.coli 16s rRNA were disregarded, since E. coli is the organism closest to Mycoplasm sp., therebyensuring no cross-reactions with E. coli and the other organisms listed in Table 5. As shown in Figure2, three sequence stretches were identified that met the criteria mentioned above.In a second analysis, sequences were analyzed within the identified three regions.Surprisingly, no primers and probes could be designed in the first two regions highlighted in Figure 1,i.e. in the region between 500 and 600 bp, and in the region at around 800 bp, although all threeregions showed homology between mycoplasma species. Instead, primers and probes were designed inthe sequence stretch on the 16s rRNA of the third region at around 1100 bp, which further required awidening of the region to accommodate all three of the forward primer, the probe, and the reverseprimer. Details of this region are presented in Figure 2. Example 2: Primer design Several primers were designed in the regions identified and fitness for PCR was determined.Regarding the forward primers, no sequence strictly identical across species could be identified, andprimers that could accommodate mismatches with target DNA had to be selected. As shown in Table 6below, several primers were selected, with one to three mismatches depending on the mycoplasmatarget sequence. A selection filter based on the elimination of primers with unfavorable primer dimerformation and primers with temperature resistant hairpin structures (Tm > 50°C) led to the selection ofa limited number of primers for subsequent experiments.Table 6: Characteristics of forward primersType Primer SEQ name Sequence IDBp GC% Dimer Tm1 Tm2 TmHPNO FwMyco1 CCGCACAAGCGGTGGAGCATGTGG 3 24 67 ok 74,6 72,7 71FwMyco2 ACCCGCACAAGCGGTGG 4 17 71 ok 62,7 67,4 71FwMyco3 ACCCGCACAAGCGGTG 5 16 69 ok 58,7 65,0 71FwMyco4 CCCGCACAAGCGGTG 6 15 73 ok 57,6 62,9 71FwMyco5 CCCGCACAAGCGGTGG 7 16 75 ok 61,9 65,5 718FwMyco6 CCGCACAAGCGGTGGA 8 16 69 ok 59,9 64,6 71CGGTFwMyco7 CACAAGCGGTGGAGCATGT 9 19 58 ok 59,3 65,0 43FwMyco8 ACAAGCGGTGGAGCATGTG 10 19 58 ok 59,3 65,0 43FwMyco9 ACAAGCGGTGGAGCATGTGG 11 20 60 KO 62,9 67,1 43FwMyco10 CAAGCGGTGGAGCATGTG 12 18 61 ok 58,3 63,2 41FwMyco11 AAGCGGTGGAGCATGTGG 13 18 61 ok 59,2 64,7 41FwMyco12 CGGTGGAGCATGTGGTTTAATT 14 22 46 KO 59,7 63,5 13FwMyco13 CACAAGTGGTGGAGCATGTG 15 20 55 ok 57,1 63,3 44FwMyco14 CACAAGTGGTGGAGCATGTGG 16 21 57 ok 61,0 65,3 41FwMyco15 CACAAGTGGTGGAGCATGTGGT 17 22 55 ok 61,8 66,9 41FwMyco16 ACAAGTGGTGGAGCATGTG 18 19 53 ok 53,8 62,4 331FwMyco17 ACAAGTGGTGGAGCATGTGG 19 20 55 ok 58,0 64,7 33TGGTFwMyco18 ACAAGTGGTGGAGCATGTGGT 20 21 52 ok 58,9 66,3 33FwMyco19 ACAAGTGGTGGAGCATGTGGTT 21 22 50 ok 60,3 66,7 33FwMyco20 CAAGTGGTGGAGCATGTGG 22 19 58 ok 57,0 62,9 14FwMyco21 CAAGTGGTGGAGCATGTGGT 23 20 55 ok 58,0 64,7 14FwMyco22 CAAGTGGTGGAGCATGTGGTT 24 21 52 ok 59,5 65,0 14FwMyco23 CAAGTGGTGGAGCATGTGGTTT 25 22 50 ok 60,8 65,4 141FwMyco24 GCACAAGCGGTGGATCATG 26 19 58 ok- 59,6 63,4 50CTTTFwMyco25 GCACAAGCGGTGGATCATGT 27 20 55 ok 60,5 65,2 50FwMyco26 CACAAGCGGTGGATCATGT 28 19 53 ok 56,4 62,5 44FwMyco27 CACAAGCGGTGGATCATGTT 29 20 50 ok 58,0 63,0 44FwMyco28 CACAAGCGGTGGATCATGTTG 30 21 52 ok 60,9 63,7 44FwMyco29 ACAAGCGGTGGATCATGTTG 31 20 50 ok 58,0 63,0 33FwMyco30 ACAAGCGGTGGATCATGTTGT 32 21 48 ok 58,9 64,7 33FwMyco31 ACAAGCGGTGGATCATGTTGTT 33 22 46 ok 60,2 65,1 33FwMyco32 CAAGCGGTGGATCATGTTG 34 19 53 ok 57,0 61,1 14FwMyco33 CAAGCGGTGGATCATGTTGT 35 20 50 ok 58,0 63,0 14FwMyco34 GCACAAGTGGTGGAGCATGT 36 20 55 ok 58,2 65,2 50FwMyco35 GCACAAGTGGTGGAGCATGTT 37 21 52 ok 59,6 65,5 50FwMyco36 GCACAAGTGGTGGAGCATGTTG 38 22 55 ok 62,4 66,1 50FwMyco37 CACAAGTGGTGGAGCATGT 39 19 53 ok 53,8 62,4 44FwMyco38 CACAAGTGGTGGAGCATGTT 40 20 50 ok 55,6 62,9 44FwMyco39 CACAAGTGGTGGAGCATGTTG 41 21 52 ok 58,6 63,7 443FwMyco40 CACAAGTGGTGGAGCATGTTGC 42 22 55 ok 62,4 66,1 43TGTCFwMyco41 ACAAGTGGTGGAGCATGTT 43 19 47 ok 52,3 62,0 33FwMyco42 ACAAGTGGTGGAGCATGTTG 44 20 50 ok 55,6 62,9 33FwMyco43 ACAAGTGGTGGAGCATGTTGC 45 21 52 ok 59,6 65,5 37FwMyco44 ACAAGTGGTGGAGCATGTTGCT 46 22 50 ok 60,6 66,9 43FwMyco45 CAAGTGGTGGAGCATGTTG 47 19 53 ok 54,5 61,1 14FwMyco46 CAAGTGGTGGAGCATGTTGC 48 20 55 ok 58,7 63,8 42FwMyco47 CAAGTGGTGGAGCATGTTGCT 49 21 52 ok 59,8 65,3 57Tm1 calculated using PrimerExpres3.0 Tm2, GC% and TmHP calculated with IDT web site program with qPCR parameters selected on batch analysis. TmHPis melting temperature of Hairpin. Tm was calculated assuming no mismatch with targets. Parameters highlighted in grey led to primer counterselection. Primers in bold were selected for further assays.A similar approach led to the identification of reverse primers with sequences andcharacteristics presented in Table 7 below. Primer RevMyco1* was chosen for showing the best Tmcriteria. Table 7: Characteristics of reverse primers The forward and reverse primers identified to fulfil all criteria are presented in Table 8 below.For clarity, Tm was calculated assuming no mismatch with targets.Table 8: Forward and reverse primers used in the experimental assessment.Primer name Sequence SEQ ID NO bp GC% Dimer Tm1 Tm2 TmHPFwMyco7 CACAAGCGGTGGAGCATGT 9 19 58 ok 59,3 65,0 43FwMyco11 AAGCGGTGGAGCATGTGG 13 18 61 ok 59,2 64,7 41FwMyco14 CACAAGTGGTGGAGCATGTGG 16 21 57 ok 61,0 65,3 41FwMyco17 ACAAGTGGTGGAGCATGTGG 19 20 55 ok 58,0 64,7 33FwMyco27 CACAAGCGGTGGATCATGTT 29 20 50 ok 58,0 63,0 44FwMyco30 ACAAGCGGTGGATCATGTTGT 32 21 48 ok 58,9 64,7 33FwMyco39 CACAAGTGGTGGAGCATGTTG 41 21 52 ok 58,6 63,7 44FwMyco43 ACAAGTGGTGGAGCATGTTGC 45 21 52 ok 59,6 65,5 37FwMyco46 CAAGTGGTGGAGCATGTTGC 48 20 55 ok 58,7 63,8 42RevMyco1* CTGACGACAACCATGCACCA 50 20 55 ok 60,1 64,8 29 Tm1 from PrimerExpres3.0. Tm2, GC% and TmHP from IDT web site with qPCR parameters selected on batch analysis.Example 3: Primer assessment by dye incorporation-based PCR on various organismsPrimers were first tested in SYBR green-based PCR in order to select the best sets, prior todesigning, selecting and optimizing probes to be used in more specific TaqMan PCR.DNA samples from different organisms were acquired as described in Table 9 below. Forsome DNA samples, lyophilized genomic DNA was acquired at the concentration indicated by the manufacturer (10 ng per tube). Alternatively, lyophilized qPCR standards provided as 108 copies / tubewere used. For E coli, Homo sapiens and CHO samples, lyophilized genomic DNA was purchased andresuspend at 7x1010, 7x109and 1.6x106genome copies / µL. In all cases, DNA solutions were diluted to reach a concentration of 3x103gene copies / µL and used for primer characterization. Table 9: Organisms and DNA sources used for primer assessment Organism Strain ATCC NCTC Cat. No. SupplierPG-8A ATCC 23206 NCTC10116 52-0116 Minerva BiolabsG230 ATCC 23838 NCTC10129 52-0129 Minerva BiolabsPG18 ATCC 19989 NCTC10117 52-0117 Minerva BiolabsPG31 ATCC 19610 NCTC10115 52-0115 Minerva BiolabsPG21 ATCC 23114 NCTC10111 51-0111 Minerva BiolabsDBS1050 ATCC 29052 NCTC10130 52-0130 Minerva BiolabsCH19299 ATCC 23714 NCTC10112 52-0112 Minerva BiolabsFH ATCC 15531 NCTC10119 52-0119 Minerva BiolabsPG20 ATCC 23064 NCTC10113 51-0113 Minerva BiolabsWVU1835 ATCC 25204 NCTC10124 51-0124 Minerva BiolabsR8-A2 ATCC 27556 NCTC10164 52-0164 Minerva Biolabs ATCC 14579 51-0031 Minerva BiolabsBacillus subtilis ATCC 6051 51-0010 Minerva BiolabsClostridium* perfringens ATCC 13124 2108-004756 Minerva BiolabsEscherichia coli ATCC 11303 NCTC14380 J14380 Thermo FisherLactobacillus* acidophilus ATCC 4796 51-1723 Minerva BiolabsMicrococcus luteus ATCC 4698 51-0030 Minerva BiolabsStaphylococcus aureus ATCC 12600 51-0231 Minerva BiolabsStaphylococcus saprophyticus ATCC 15305 2120-20229 Minerva BiolabsStreptococcus* bovis ATCC 33317 2122-20480 Minerva BiolabsStreptococcus* pneumoniae ATCC 33400 51-0566 Minerva BiolabsHomo sapiens 11691112001 RocheCricetulus griseus 9A9wt NA NA NA Sanofi* Required by PhEu 2.6.7 All forward primers were used in PCR reactions with the unique reverse primer RevMyco1* as shown in Table 8. For each reaction, 20,000 copies of genomic DNA were used. The PCR Cqvalues obtained are presented in Table 10 below.Table 10: Cq values of primer combinations used in qPCR experiments on the indicated organisms’ reference DNA samples. Couple Name hyorhinis arginini fermentans orale pneumoniae salivarium gallisepticum synoviae hominis laidlawii citri Forward primers 27, 30, 39 and 46 produced the highest Cq values across all the speciesinvestigated. The best set was therefore chosen among forward primers 7, 11, 14 and 17. qPCR performed with Forward Primer 7 (Fwd7) displayed Cq values significantly below 20 for allorganisms except for Mycoplasma hominis. The analysis of the PCR reactions by PAGE together with the melting curves further confirms the presence of a single amplicon per reaction of the expected sizeand Tm (Fig. 3).Example 4: Hydrolysis probe design The target sequence for the probes was chosen in the region shown in Figure 2. The task wasto encompass a homologous sequence among mycoplasma species with significant mismatch to otherorganisms. Given the nature of the DNA sequences, it was not possible to design a 23-nucleotide probe with a Tm of about 70°C. It was therefore attempted to design longer probes of up to 40 nucleotides but such probes invariably encompassed non-homologous sequences in the 5’ region. In order to overcome these limitations, two strategies were followed: 1) generating long probes withinternal quenchers (ZEN probes), and 2) using short probes (about 23 nucleotides) and increasing Tmby the use of chemical modifications such as Locked Nucleic Acids (LNA) or minor grove binding(MGB) moieties to tighten the probe / target interaction. Plain long probes, probes with hightemperature-resistant hairpin structures (Tm > about 45°C), and unfavourable primer dimer formationwere excluded. Table 11 below lists the designed probes.Table 11: Hydrolysis probes designed for the experimental assessment Probe name Sequence SEQ Bp GC% Dimer Tm1 Tm2 TmHPID NOSMyco1 ZEN GCAAAGCTATAGAGATATAGTGGAGGTT 54 32 38 KO 60,7 65,8 50AACA SMyco2 ZEN GCAAAGCTATAGAGATATAGTGGAGGTT 55 31 39 KO 58,9 64,6 50AAC SMyco3 ZEN CAAAGCTATAGAGATATAGTGGAGGTTA 56 31 36 KO 58,2 64,1 50ACA SMyco4 ZEN CAAAGCTATAGAGATATAGTGGAGGTTA 57 40 38 ok 66,0 68,3 34ACAGAATGACAG SMyco4bis CAAAGCTATAGAGATATAGTGGAGGTTA58 40 40 ok 66,2 68,9 27ZEN ACAGAGTGACAG SMyco5 LNA TATAGTGGAGGTTAACAGAATG 59 22 36 ok 47,9 68,7 46SMyco5bisTATAGTGGAGGTTAACAGAGTG 60 22 41 ok 47,8 68,6 22LNA SMyco5 MGB TATAGTGGAGGTTAACAGAATG 61 22 36 ok 70,0 57,4 46SMyco5bisTATAGTGGAGGTTAACAGAGTG 62 22 41 ok 68,0 58,8 22MGB SMyco6 MGB TATAGAGATATAGTGGAGGTTAACAGAG 63 37 ok 72,0 63,1 41TG SMyco7 MGB TATAGAGATATAGTGGAGGTTAACAGA 64 33 ok 70,0 60,6 41SMyco8 MGB TATAGAGATATAGTGGAGGTTAACAG 65 35 ok 69,0 59,3 41SAcho1 LNA TAAGTTCGGAGGCTAACAGATGT 67 44 ok 56,0 68,6 39Tm1 from PrimerExpres3.0, adapted for MGB probe Tm calculation. Tm2, GC%, TmHP from IDT web site with qPCR parameters selected on batch analysis, adapted for LNA probe Tm calculation. Underlined bases were LNA modified. Bold sequences were selected for evaluation. Example 5: Probe assessment by hydrolysis probe-based PCR on various organisms Probes selected from Table 11 were tested with the unique Fwd7 / Rev1* primer set (Table 10)in order to select the best primer / probe combination. As shown in Tables 12 and 13 below, besidesAcholeplasma laidlawii, all other mycoplasma species were detected by LNA and MGB probes, although the Smyco5 MGB probes failed to detect Mycoplasma gallisepticum DNA. No or onlylimited background signal (Cq >37) was generated on DNA samples from other species.Table 12: Evaluation of LNA and MGB probes on Mycoplasma DNA samples Probe name hyorhi argini fermenta nis ni ns orale pneumon salivariu gallisepticu synovia homini laidlaw iae m m e s ii citri Table 13: Evaluation of LNA and MGB probes on DNA samples of other organisms Probe name pneumoni bovi subtili cereu perfringe acidophil saprophytic aureu Luteucoli sapienCHO ae s s s ns us us s s s Smyco5 LNA N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D.Smyco5bisN.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D.LNA Smyco5 MGB N.D. N.D. N.D. N.D. 40,17 N.D. N.D. N.D. N.D. 37,7 N.D. N.D.The SAcho1LNA probe which is more specific to Acholeplasma laidlawii by design was alsoassessed in a similar assay. As shown in Tables 14 and 15 below, this probe successfully detected theamplification of Acholeplasm lindlawii DNA, and did not detect any other DNA sample, with nobackground detection on DNA from other species. Furthermore, when used in a single mix, the Smyco5bis LNA and SAcho1LNA probes detected the DNA of all mycoplasma species with no background detection on DNA from other species. Table 14: Evaluation of LNA probes on Mycoplasma DNA samplesProbe name hyorhi argini fermenta oral pneumon salivariu Gallisepticu synovia homini laidlaw nis ni ns e iae m m e s ii citri Table 15: Evaluation of LNA probes on DNA samples of other organisms Probe name pneumoni bovi subtili cereu perfringe acidophil saprophytic aureu Luteucoli sapienCHO ae s s s ns us us s s s Smyco5bisN.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D.LNA SAcho1 LNA N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D.Smyco5bisN.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D. N.D.LNA + A particularly preferred combination of primers and probes for mycoplasma detection is shown in Table 16 below.Table 16: Preferred primer / probe combination SEQ Name SequenceIDBp GC% Dimer Tm1 Tm2 TmHPNO FwMyco7 CACAAGCGGTGGAGCATGT 9 19 58 Ok 59,3 65,0 43RevMyco1* CTGACGACAACCATGCACCA 50 20 55 Ok 60,1 64,8 46SMyco5bis LNA TATAGTGGAGGTTAACAGAGTG 60 22 41 Ok 47,8 68,6 22SAcho1 LNA TAAGTTCGGAGGCTAACAGATGT 67 23 44 Ok 56,0 68,6 39Tm1 from PrimerExpres3.0, adapted for MGB probe Tm calculation. Tm2, GC%, TmHP from IDT web site with qPCR parameters selected on batch analysis, adapted for LNA probe Tm calculation. Underlined bases were LNA modified. Example 6: Control probes Two gBlocks (double stranded DNA fragments) were synthesized with structures described in Figure 4 and Table 17. The IPC (internal positive control) is added to all samples and contains thesequences that allow the annealing of the Mycoplasma PCR primers, and the annealing of a unique probe (TraA). This construct generates positive signals in the StraA channel in all samples and serves as positive PCR control. The DPC (discriminatory positive control) construct is used instead of sample DNA in aseparate reaction and contains the sequences that allows the annealing of the Mycoplasma PCR primers, the annealing of the Mycoplasma specific probes and the annealing of another unique probe (AtPSY). This construct generates positive signal in the Mycoplasma probes channel and confirms the presence of mycoplasma specific probes in the PCR mix. In addition, fluorescence in the AtPSY probe chanel should be detected in this sample only. Samples positive in the AtPSY probe channel demonstrate sample contamination with this construct. All control constructs are purchased from IDT as double strand gBlocks. Table 17: IPC and DPC sequences Construct nameSequence SEQSize (bp) ID NO CGTCATCGGATCTCGAGGACCTGGCTTTAGAGCCTTGGAGCACACC AAATACTCCTGTTGCGGGCACTGCAGAAACCCAGAACACTGGGGA AGCTGGTTCCAAAGCCTGCCAAGATGGTCAACTGAGCCCAACTTGG TTTCACAAGCGGTGGAGCATGTGGTTTAATTTGAAGATACGCGTA GAACCTTACCCACTCTTGACATCTTCTGCAAAGCTATAGAGATAMyco DPC - gBlockTAGTGGAGGTTAACAGAATGATTTAAGTTCGGAGGCTAACAGA TGTATTCCGACTCGCAGAACCGGAACGATTGATGGTGCATGGTTG70 494TCGTCAGTTTGAACTTGGACTAAGGTACGATGGCGCCTCCAGCTAA AAGAGCTAAAAGAGGTAAGGGTTTAAGGGATGGTTGGTTGGTGGG GTATTAATGTTTAATTACCTGTTTTACAGGCCTGAAATCACTTGGTT TTAGGTTGGGTGCCTCCTGGCTACAAGTACCTGGGACCACGT CGTCATCGGATCTCGAGGACCTGGCTTTAGAGCCTTGGAGCACACC AAATACTCCTGTTGCGGGCACTGCAGAAACCCAGAACACTGGGGA AGCTGGTTCCAAAGCCTGCCAAGATGGTCAACTGAGCCCAACTTGG TTTCACAAGCGGTGGAGCATGTGACAGAGATCGAGGAGGATTTGAG AGGCGCCCGTCAAAAAGAAGTCCGTCACACGCAGTGATCCCGGCTMyco IPC - gBlockGCTGCGTCACATTCTGATGATGTTCTTCCCGCTAAGACTTCAGCGA68 473GCCGCTTGGTGCATGGTTGTCGTCAGTTTGAACTTGGACTAAGGTA CGATGGCGCCTCCAGCTAAAAGAGCTAAAAGAGGTAAGGGTTTAA GGGATGGTTGGTTGGTGGGGTATTAATGTTTAATTACCTGTTTTACA GGCCTGAAATCACTTGGTTTTAGGTTGGGTGCCTCCTGGCTACAAG TACCTGGGACCACGT Bold sequences correspond to Mycoplasma / Acholeplasma reference sequences. Underlined and italicized sequences correspond to Mycoplasma / Acholeplasma-specific probes and primers, respectively. Gray highlighted sequences correspond to sequences of AtPSY (DPC) and TraA (IPC). Example 7: Probe modifications and PCR reaction parameters All primers and probes are purchased from IDT. Probes were linked to fluorochromes and quenchers as shown in Table 18. Table 18: Probe sequences and chemical modification Name Sequence SEQ ID NO Fluorochrome / quencherFwMyco7 CACAAGCGGTGGAGCATGT 9 N.A.RevMyco1* CTGACGACAACCATGCACCA 50 N.A.SMyco5bis LNA TATAGTGGAGGTTAACAGAGTG 60 FAM / IABkFQSAcho1 LNA TAAGTTCGGAGGCTAACAGATGT 67 FAM / IABkFQSAtPSY CCGACTCGCAGAACCGGAACGA 71 HEX / IABkFQStraA CGCAGTGATCCCGGCTGCTG 69 The PCR premix was prepared and PCR reactions were performed as described in Table 19.5µL of unknown DNA sample or DPC were added. Code UNGase is purchased from ArcticZymes. Table 19: PCR reaction mixture Premix [C]initial [C]final Amount (µL)for 1 reaction Luna Universal Probe qPCR Master Mix (2x) 2x 1x 10.0Code UNGase 1 u / µL 1 u / 100µL 0.2Water / Qsp 15µL 3.48Fw Myco7 100 µM 400 nM 0.08Rev Myco1* 100 µM 400 nM 0.08S Myco5 bis 100 µM 200 nM 0.04S Acho1 100 µM 200 nM 0.04SAtPSY 100 µM 200 nM 0.04StraA 100 µM 200 nM 0.04gBlock IPC 200 cp / µL 200 cp 1Final volume 15.0The cycling conditions used are described in Table 20 below.Table 20: Cycling conditions for PCRStep Temperature Time CycleUNG 40°C 120s 1Activation 90°C 60s 1Denaturation 90°C 15sAmplification 60°C 30s45 Example 8: Determining detection and quantification limits As described above, probes and primers were developed with purified genomic DNA used at known concentrations in PCR reactions (15,000 to 20,000 genome copies per reaction). However, guidelines ask for assays capable of detecting a defined number of colony forming unit (CFU) / mL. Lyophylized mycoplasma samples of known CFU contents were therefore purchased from vendors asshown in Table 21 below, and tested together with various amounts of reference DNA (see Table 6) inorder to link CFU to genome copies and to determine the limit of quantification (LOQ) and the limit ofdetection (LOD) of the method of the present invention, expressed in CFU / mL.Table 21: Mycoplamsa colony reference standards for confirming LOD Organism Strain ATCC NCTC Cat. No. SupplierPG-8A ATCC 23206 NCTC10116 102-8003 Minerva BiolabsG230 ATCC 23838 NCTC10129 102-1003 Minerva BiolabsPG18 ATCC 19989 NCTC10117 102-6003 Minerva BiolabsPG31 ATCC 19610 NCTC10115 102-3003 Minerva BiolabsDBS1050 ATCC 29052 NCTC10130 102-7003 Minerva BiolabsCH19299 ATCC 23714 NCTC10112 102-2003 Minerva BiolabsFH ATCC 15531 NCTC10119 102-4003 Minerva BiolabsPG20 ATCC 23064 NCTC10113 102-1103 Minerva BiolabsWVU1835 ATCC 25204 NCTC10124 102-5003 Minerva BiolabsR8-A2 ATCC 27556 NCTC10164 102-9003 Minerva Biolabs In a first step, the LOQ of the method was determined on each reference DNA samples listedin Table 9. Briefly, reference DNA of known concentrations were diluted and PCR was performed asdescribed herein to correlate Cq to DNA copies. The results obtained for each mycoplasma DNAsample are shown in Table 22 below. All samples were positive in the IPC channel at the expected Cqvalue (data not shown). The LOQ for all mycoplasma was set to the second to last reference DNAdilution for which the qPCR software was able to calculate a Cq. All LOQs were therefore set to 100mycoplasma genome copies per reaction, except for M. synoviae for with the LOQ was set to 1,000mycoplasma genome copies per reaction. Table 22: Calibration curves performed on mycoplasma reference DNA 10000 27,44 26,30 26,67 28,85 24,26 27,16 27,71 26,52 26,1810000 27,67 26,32 26,69 29,96 24,63 27,03 27,80 26,33 25,781000 31,49 29,30 30,18 33,60 27,90 30,42 31,33 29,88 29,391000 31,49 29,31 30,14 33,02 27,63 30,61 31,10 29,61 29,28 In a second step, the method was applied on the colony reference standards listed in Table 21 and all Cq values were determined. The equations calculated from the calibration curves (Table 22) were then used to determine the equivalence between CFU and genome copies. The number of CFU corresponding to the LOQ of the method determined on reference DNA standards was then calculated as the LOQ expressed in CFU / mL, taking into account a maximum sample volume 5µL. As is shownin Table 23 below, LOQ and LOD were <100 and <10 CFU / mL, respectively. The LOD < 10CFU / mL matches the requirements set forth in Chapter 2.6.7 of the European Pharmacopoeia. Example 9: Identification of genome regions to be targeted by PCR Organisms investigated are listed in Table 24 below. These include the 4 MMV serotypes (p, i, m & c) and parvoviruses from close species which presence should be investigated in various cell substrates taken from the production workflow: Upstream & Down Stream Processing (for viral clearance), Master Cell Bank, Working Cell Bank, Unprocessed Bulk, End Of Production Cells for viral safety, as indicated in various guidelines. Table 24 - Sequences of organisms addressed in this study. In order to identify the best genomic region to be targeted by PCR and ensure specific MMV detection, full genome of parvovirus listed in Table 24 were retrieved from NCBI website ( www.ncbi.nlm.nih.gov) and compared. Afirst pass analysis focused on MMV genomes aimed at identifying 300 bp stretches with80% homology across genomes where primers and hydrolysis probes of 20 and 23 nucleotides, respectively, could be designed. As shown in Figure 5, only one stretch was identified that met the criteria mentioned above. A highly conserved region of around 315 bp identified at position 2002-2316 (NC_001510.1). Coding sequences for NS1, NS2, VP1, VP2, VP3 and VP4 proteins are present in this strategic position and it is just before a “VP intron” where various primers for a putative future RT-qPCR could be designed. In a second filtering approach, sequences were analyzed within this 315 bp domains whereprimers and probes could be designed for all serotypes, with Tm of 60°C and 70°C, respectively. Sequences that would generate primer dimers and hairpin structures >50°C and amplicon >100 bpwhere disregarded. Once selected, zones of interest were again checked against sequences of parvoviruses listed in Table 24. Details of this region are presented in Figure 6.Example 10: Primer design Primer sets and probes were designed and tested as listed in Table 25 below.

[0016] Sequences used for both, the MMV assay and for the mycoplasma assay are shown in Table27 below. Table 27: List sequences for the MMV assay and common with Mycoplasma Assay TTCTGATGATGTTCTTCCCGCTTGAAGAAAGACTTCAGCGA sequences of interest for internal control. ATCTCGAGGACCTGGCTTTAGAGCCTTGGAGCACACCAAAT GCGGGCACTGCAGAAACCCAGAACACTGGGGAAGCTGGTTC CCAAGATGGTCAACTGAGCCCAACTTGGTTTCACAAGCGGT SEQ ID NO: 68. Used as an GACAGAGATCGAGGAGGATTTGAGAGGCGCCCGTCAAAAAG internal control to discriminate ACACGCAGTGATCCCGGCTGCTGCGTCACATTCTGATGATG false negative signals. CTAAGACTTCAGCGAGCCGCTTGGTGCATGGTTGTCGTCAG 473Contains Mycoplasma and MMVGGACTAAGGTACGATGGCGCCTCCAGCTAAAAGAGCTAAAA primers, and Episome F’ TraA GTTTAAGGGATGGTTGGTTGGTGGGGTATTAATGTTTAATT primers and probe (StraA) ACAGGCCTGAAATCACTTGGTTTTAGGTTGGGTGCCTCCTG sequences ACCTGGGACCACGT TGGAGCATGTGACAGAGATCGAGGAGGATTTGAGAGGCGCC SEQ ID NO: 116. Sequences CGTCAAAAAGAAGTCCGTCACACGCAGTGATCCCGGCTGCTGCGTCACAT MMV) containing primers and probe TCTGATGATGTTCTTCCCGCTAAGACTTCAGCGAGCCGCTTGGTGCATGG 160 sequences of interest for internal TTGTCGTCAG control Bolt sequences are primersHighlighted sequences are probesUnderlined sequences are MMV specificDouble underlined sequences are Mycoplasma specificItalicized sequences are common to MMV and Mycoplasma assay.Figure 7 shows the different positions of the primers and probes on control constructs.Example 11: MMV detection method qualification To demonstrate the specificity of the method, various gDNA extracts were used as matrix foramplification in parallel of MMV vDNA (see Table 28 below). A specific triplex assay was developedto allow for the detection of these gDNA in samples tested for MMV method specificity. MMV andgDNA quantification was performed at the same time and in the same plate using two PCR mixes(Mix 1 targeting MMV and Mix 2 targeting human, E. coli and CHO gDNA concomitantly). To becomparable, 1,500 to 2,000 copies of each target were added to the matrix, taking in account the typeof genome of each species (dsDNA ssDNA, haploid or diploid). Amplification results are shown inFigures 8 and 9. Amplification curves in Fig. 8 are as expected: MMV Mix1 amplifies neither human,nor E. coli or CHO gDNA. It amplifies only the desired target at a specific channel. For IPC (Cy5 channel), not all amplifications reach the same plateau. This is due to heterogeneous Probe and Primerconsumption attributable to the design of the method. This is unproblematic because all Cq are similarand within SD < 0,5 as expected. Similarly, amplification curves in Figure 9 are as expected: gDNAMix 2 amplifies neither MMV nor DPC nor IPC. It amplifies only gDNAs and amplification is seen in the specific channel. In conclusion, the method is specific for MMV. Table 28: Material used as DNA matrix for method evaluation Organism Reference Provider Batch ConcentrationMouse Minute Virus ATCC VR-1346 ATCC 3382456 1.6 x 103 TCID50 / µLHomo sapiens 11691112001 ROCHE N.A. 200 ng / µLEscherichia coli 14380 ThermoFisher 4229216 2 µg / µLCricetulus griseus CHO rWCB Sanofi N.A. 4.47 x 103 cells / µL Subsequently, relevant amplification products were analyzed by 15% PAGE to assess thequality of the amplification. Results are shown in Figure 10. Visualization of amplification productsshows clear results for both MMV and gDNA mixes. Number of bands and sizes observed complywith the expected results. For PCR Mix 1, the IPC band (about 150 bp) is present in all wells (01 to07), not in negative control well 08 (MMV mix with no DNA nor IPC). Well 02 contains in additionto IPC band the viral band at about 70 bp, and well 03 contains the discriminatory band at about 90bp.Wells 05, 06 and 07 which are gDNA do not generate other significative bands. The primer dimerband is observed on all wells (01 to 08). For PCR Mix 2, several primer dimer bands are observable as no primer optimization was performed. This assay was designed to check for presence of gDNAs in the assay. There is no significative bands on wells 09 to 12 which are reagents involved in MMVassay. Expected bands at different sizes are observed in well 13 (human) at about 59 bp, in well 14 (E.coli) at about 62 bp, and in well 15 (CHO) at about 81 bp. The 15% PAGE analysis confirms thatqPCR amplification products are specific for MMV. The limit of detection of a qPCR method is by definition one copy per reaction of the targetedDNA. For determining detection limits of the present method, a 10-fold serial dilution of DPC and IPCwas performed down to about 0,08 copy / reaction. The last 7 points (called G4 to G10) were analyzedin hexaplicates. For each dilution point, at least 3 replicates must give a signal to be considered.Results are summarized in Tables 29 and 30 below.Table 29: Mean Cq values for DPC serial dilutions FAM HEXName Copy Cq SD RSD Cq SD RSD RemNTC 0 NA NA NA NA NA NAG10 0,08 ND ND ND ND ND ND < LODG9* 0,8 38,5 1,0* 2,7% 38,2 1,0* 2,6% = LODG8 8,0 36,5 0,3 0,9% 36,3 0,3 0,9% = LOQG7 79,5 33,0 0,1 0,4% 32,8 0,1 0,4%G6 795 29,7 0,1 0,2% 29,5 0,1 0,3%G5 7950 26,2 0,0 0,0% 26,1 0,0 0,1%G4 79500 22,9 0,0 0,1% 22,7 0,0 0,1%* 3 of 6 replicates were detected ND: No detection Table 30: Mean Cq values for IPC serial dilutions Cy5 Name Copy / Cq SD RSD Remreaction NTC 0 NA NA NAName Copy / Cq SD RSD Remreaction G10 0,06 ND ND ND < LODG9** 0,6 39,2 1,0** 2,6% = LODG8 5,8 36,8 0,6*** 1,7% = LOQG7 57,5 33,6 0,1 0,3%G6 575,0 30,1 0,1 0,2%G5 5750,0 26,7 0,0 0,0%G4 57500,0 23,3 0,0 0,1%** 4 of 6 replicates were detected, 2 of 6 are out of range *** Accepted SD for calibration ND: No detection In summary, the detection limit for both samples is fixed at one copy per reaction.For establishing the limit of quantification, data from the sample preparation as described inExample 11 above was used. A calibration curve was made for points with a SD < 0.5 (G4 to G8).Intercepts for all targets are in the same range (mean 39.43) with an SD of 0,08 (<0.5). While keepingthe last point G8 for Cy5 target that has a SD >0.5, all the parameters comply with acceptance criteriafor all the targets: Slope -3.32 (±0,3) and r² > 0.98. As shown in Fig. 11, all curves were perfectly superposed with a slight SD increase at lower concentration. This observation is mostly observed for the Cy5 reporter asexpected. Table 31 below shows the variability of the lower point at eight copies. Taken together, thelimit of quantification was estimated at ten copies per reaction.Table 31: Variability of lower point: 8 copies SampleName FAM HEXG8_1 36,00 35,86G8_2 36,55 36,40G8_3 36,16 36,00G8_4 36,77 36,60G8_5 36,74 36,59G8_6 36,70 36,49SD 0,33 0,32Robustness of the method was evaluated by performing a 10-fold viral sample dilution.Followed by DNA extraction added with about 4x105 cells or TE (10; 0,1) pH8,0. Extracts werequantified by droplet digital PCR to link TCID50 / mL value to copy / µL unit. Each extracted DNAsample was then cycled in triplicate. To comply, no significative difference should be observablebetween Cq values of MMV extracted with cells or TE (10;0,1) pH8,0. Plus, ΔCq should be < 1.Results are summarized in Tables 32 to 35 below.Table 32: Extraction serial dilution MMV + Cells MMV + TEName TCID50 / mL Log (Q) Mean Cq SD Mean Cq SD ΔCqF 0,8 0,2 29,16 0,08 28,78 0,11 0,38E 8 1,2 25,79 0,38 25,80 0,05 0,01D 80 2,2 22,61 0,06 22,19 0,03 0,42C 800 3,2 19,29 0,27 18,56 0,06 0,74B 8000 4,2 15,65 0,07 15,43 0,03 0,23A 80000 5,2 12,32 0,45 11,94 0,03 0,38At each dilution point, extraction of MMV added with cells or TE returned similar Cq values.ΔCq is < 0.5 for 5 of 6 dilution points and < 1 for all. This means that there is no significative impacton MMV detection and quantification when the viral genetic material is extracted from the buffer (TE) or from a complex medium (cell suspension). Table 33: Dilution curve parameters Name MMV + Cells MMV + TESlope -3,37 -3,40Intercept 30,93 30,66r² 0,998 0,999E 98% 97%Table 33 shows that although it is an extraction, these parameters perfectly meet thespecification of a calibration curve as described above. These observations lead to the conclusion that the method is robust. Intercept value will depend of the unit used for the variable x of the curve, in that case the infectivity "TCID50 / mL". This unit is not commonly used for qPCR, this is why it is preferable toreformat Tables 32 and 33 with a genome equivalent "copy" unit determined with ddPCR absolutequantification as shown in the following Tables 34 and 35.Table 34: Extraction serial dilution reformattedMMV + Cells MMV + TEDilution Copy Log (cp) Mean Cq SD Mean Cq SD ΔCqF 2237 3,3 29,16 0,08 28,78 0,11 0,38E 22369 4,3 25,79 0,38 25,80 0,05 0,01D 223688 5,3 22,61 0,06 22,19 0,03 0,42C 2236875 6,3 19,29 0,27 18,56 0,06 0,74B 22368750 7,3 15,65 0,07 15,43 0,03 0,23A 223687500 8,3 12,32 0,45 11,94 0,03 0,38Table 35: Dilution curve parameters reformatted ("copy" means copy per reaction)Name MMV + Cells MMV + TESlope -3,37 -3,40Intercept 40,51 40,33r² 0,998 0,999E 98% 97%In the reformatted tables, no changes in Cq, SD, Slope, r² and E are shown. As expected, onlyIntercept values were modified in calculation and they are now very close to those shown in Table 33.The calibration curves for two different data units are shown in Fig. 11. After datareformatting, a 10 Cq drift is observed meaning about 3Log10 difference in absolute value. Taking MMV CoA and the quantification into account, a relationship between infectivityTCID50 / mL and Genome Copy / µL was established, which is specific to the viral sample that wasanalyzed. MMV virus stock solution was titrated at 1.6x106 TCID50 / mL. The same solution wasquantified by ddPCR at 2.24x1011 copy / mL. This means that one TCID50 / mL equals 139,805copies / mL (about 140 copies / µL).

Claims

International Patent Application under the PCT Applicant: Sanofi ZSP Ref: 589-385 PCT Claims1. A method for detecting microorganisms in a sample, comprising:(i) performing PCR on a sample suspected of comprising microorganism DNA with a PCRreaction mixture comprising (1) a first primer (P1) annealing to the reverse complement of a nucleic acid sequence ofSEQ ID NO: 1 and a second primer (P2) annealing to a nucleic acid sequence of SEQ ID NO: 2; and / or2) a third primer (P3) annealing to the reverse complement of a nucleic acid sequence ofSEQ ID NO: 109 and a fourth primer (P4) annealing to a nucleic acid sequence of SEQ ID NO: 110, and (ii) detecting a PCR product,wherein the detection of a PCR product indicates that the sample comprises microorganisms,and the absence of a PCR product indicates that the sample does not comprise microorganisms.

2. A method for detecting mycoplasma in a sample, comprising:(i) performing PCR on a sample suspected of comprising mycoplasma DNA with a PCRreaction mixture comprising a first primer (P1) annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 1 and a second primer (P2) annealing to a nucleic acid sequence of SEQ ID NO: 2; and (ii) detecting a PCR product,wherein the detection of a PCR product indicates that the sample comprises mycoplasma, and the absence of a PCR product indicates that the sample does not comprise mycoplasma.

3. The method according to claim 2, wherein: (i) P1 has a length between 18 and 24 nucleotides, preferably between 19 and 21 nucleotidesand most preferably 19 nucleotides, and / or P2 has a length between 17 and 22 nucleotides preferably between 18 and 20 nucleotides, most preferably 20 nucleotides; and / or (ii) P1 has a Tm of between 60°C and 70°C, preferably between 63°C and 69°C, morepreferably between 66°C and 68°C, and / or P2 has a Tm of between 60°C and 67°C, preferably of between 62 to 66°C and most preferably between 64°C and 65°C; and / or (iii) P1 comprises or consists of a nucleic acid sequence of SEQ ID NO: 3 to 49, and / or P2comprises or consists of a nucleic acid sequence of SEQ ID NO: 50 to 52.

4. The method according to claim 2 or 3, wherein the reaction mixture further comprises at least afirst nucleic acid probe (Probe 1) annealing to a nucleic acid sequence of SEQ ID NO: 53 or its reverse complement.

5. The method of claim 4, wherein:(i) the reaction mixture further comprises at least a second nucleic acid probe (Probe 2)annealing to SEQ ID NO: 53; and / or (ii) Probe 1 and / or Probe 2 each has a length between 20 and 42 nucleotides, preferablybetween 21 and 30 nucleotides and most preferably 22 and 24 nucleotides; and / or (iii) Probe 1 and / or Probe 2 each has a Tm of between 55°C and 70°C, preferably between58°C and 69°C, more preferably between 59°C and 68°C; and / or (iv) Probe 1 comprises or consists of a nucleic acid sequence of SEQ ID NO: 54 to 65 and / orProbe 2 comprises or consists of a nucleic acid sequence of SEQ ID NO: 66; and / or (v) Probe 1 and / or Probe 2 each comprises one or more locked nucleic acids (LNA) and / or aminor grove binding (MGB) moiety; and / or (vi) Probe 1 and / or Probe 2 each comprises a detectable label, preferably wherein Probe 1 andProbe 2 comprise the same detectable label.

6. The method according to any one of claims 1 to 5, wherein:(i) the PCR is qPCR, dPCR, ddPCR or cdPCR; and / or(ii) the PCR uses an annealing temperature of between 55°C and 65°C, preferably between58°C and 60°C; and / or (iii) the PCR comprises an activation step and / or a degradation step; and / or(iv) annealing and elongation are performed at the same temperature; and / or(v) the PCR comprises between 40 and 50 cycles of denaturation and annealing / elongation, preferably 45 cycles.

7. The method according to any one of claims 1 to 6, wherein the reaction mixture furthercomprises an internal positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleicacids of the nucleic acid sequence of SEQ ID NO: 2 and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides, wherein the intervening nucleic acid sequence preferably differs from SEQ ID NO: 53 in that neither Probe 1 nor Probe 2 anneals to the intervening nucleic acid sequence, wherein the reaction mixture preferably further comprises at least a third nucleic acid probe (Probe 3) annealing to the intervening nucleic acid sequence or its reverse complement.

8. The method according to claim 7, whereini) Probe 3 has a length between 20 and 42 nucleotides, preferably between 21 and 30nucleotides and most preferably 22 and 24 nucleotides; and / or (ii) Probe 3 has a Tm of between 55°C and 70°C, preferably between 58°C and 69°C, morepreferably between 59°C and 68°C; and / or (iii) Probe 3 comprises or consists of a nucleic acid sequence of SEQ ID NO: 69 or its reversecomplement; and / or (iv) Probe 3 comprises one or more locked nucleic acids (LNA) and / or a minor grove binding(MGB) moiety; and / or (v) Probe 3 comprises a detectable label different from the label of Probe 1 and Probe 2.

9. The method according to claim 7 or 8, wherein the internal positive control nucleic acidsequence comprises or consists of a nucleic acid sequence at least 90% identical to the nucleicacid sequence of SEQ ID NO: 68 or its reverse complement.

10. The method according to any one of claims 1 to 9, wherein the reaction mixture furthercomprises a discriminatory positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2 and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides, wherein the intervening nucleic acid sequence preferably does not differ from SEQ ID NO: 53 so that Probe 1 and Probe 2 are capable of annealing to the intervening nucleic acid sequence, wherein the reaction mixture preferably further comprises at least a fourth nucleic acid probe (Probe 4) annealing to the intervening nucleic acid sequence or to its reverse complement at a sequence that is different from the sequence to which Probe 1 and / or Probe 2anneals.

11. The method according to claim 10, whereini) Probe 4 has a length between 20 and 42 nucleotides, preferably between 21 and 30nucleotides and most preferably between 22 and 24 nucleotides; and / or (ii) Probe 4 has a Tm of between 55°C and 70°C, preferably between 58°C and 69°C, morepreferably between 59°C and 68°C; and / or (iii) Probe 4 comprises or consists of a nucleic acid sequence of SEQ ID NO: 71 or its reversecomplement; and / or (iv) Probe 4 comprises one or more locked nucleic acids (LNA) and / or a minor grove binding(MGB) moiety; and / or(v) Probe 4 comprises a detectable label different from the label of Probe 1, Probe 2, and Probe 3.The method according to claim 10 or 11, wherein the discriminatory positive control nucleic acid sequence comprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 70 or its reverse complement.The method according to any one of claims 1 to 12, wherein the sample is a biological sample preferably selected from the group consisting of a cell bank, a culture medium, a cell culture, a cell culture supernatant, a medicinal product, a vaccine preparation, blood, saliva, and sputum.A pair of primers for detecting mycoplasma in a sample comprising: a primer Pl annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 1, and a primer P2 annealing to a nucleic acid sequence of SEQ ID NO: 2.A kit for detecting mycoplasma in a sample, wherein the kit comprises the pair of primers of claim 9 and a first nucleic acid probe (Probe 1) annealing to a nucleic acid sequence of SEQ ID NO: 53 or its reverse complement, and optionally a second nucleic acid probe (Probe 2) annealing to SEQ ID NO: 53 or its reverse complement, preferably wherein the kit further comprises one or more of:(i) a PCR reaction mixture;(ii) an internal positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2 and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides, wherein the intervening nucleic acid sequence preferably differs from SEQ ID NO: 53 in that neither Probe 1 nor Probe 2 anneals to the intervening nucleic acid sequence, wherein the kit preferably further comprises at least a third nucleic acid probe (Probe 3) annealing to the intervening nucleic acid sequence or to its reverse complement;(iii) a discriminatory positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 1 and at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 2 and between these two nucleic acid sequences an intervening nucleic acid sequence of a length of at least 60 nucleotides, wherein the intervening nucleic acid sequence preferably does not differ from SEQ ID NO: 53 so that Probe 1 and Probe 2 are capable of annealing to the intervening nucleic acid sequence, wherein the kit preferably further comprises at least a fourth nucleic acid probe(Probe 4) annealing to the intervening nucleic acid sequence or to its reverse complement at a location different from the annealing of Probe 1 and / or Probe 2; (iv) means for extracting and / or purifying DNA from the sample; and(v) instructions for performing PCR with the primers.

16. The method according to any one of claims 1 to 13, the pair of primers according to claim 14 orthe kit according to claim 15, wherein the mycoplasma is one or more Mycoplasma species selected from the group consisting of Mycoplasma arginini, Mycoplasma buccale, Mycoplasma hominis, Mycoplasma orale, Mycoplasma salivarium, Mycoplasma fermentans, Mycoplasma hyorhinis, Mycoplasma synoviae, Mycoplasma pneumoniae, Acholeplasma laidlawii, Mycoplasma gallisepticum and Spiroplasma citri.

17. A method for detecting virus in a sample, comprising:(i) performing PCR on a sample suspected of comprising virus DNA with a PCR reactionmixture comprising a third primer (P3) annealing to the reverse complement of a nucleic acid sequence of SEQ ID NO: 109 and a fourth primer (P4) annealing to a nucleic acidsequence of SEQ ID NO: 110; and (ii) detecting a PCR product,wherein the detection of a PCR product indicates that the sample comprises virus, and the absence of a PCR product indicates that the sample does not comprise virus.

18. The method according to claim 17, wherein: (i) P3 has a length between 20 and 25 nucleotides, preferably between 21 and 24 nucleotidesand most preferably 23 nucleotides, and / or P4 has a length between 15 and 21 nucleotidespreferably between 16 and 20 nucleotides, most preferably 23 nucleotides; and / or(ii) P3 has a Tm of between 60°C and 70°C, preferably between 63°C and 69°C, morepreferably between 66°C and 68°C, and / or P4 has a Tm of between 60°C and 67°C,preferably of between 62 to 66°C and most preferably between 64°C and 65°C; and / or(iii) P3 comprises or consists of a nucleic acid sequence of SEQ ID NO: 104, and / or P4comprises or consists of a nucleic acid sequence of SEQ ID NO: 105.

19. The method according to claim 17 or 18, wherein the reaction mixture further comprises at leastone nucleic acid probe (Probe 5) annealing to a nucleic acid sequence of SEQ ID NO: 111 or itsreverse complement.

20. The method of claim 19, wherein:(i) Probe 5 has a length between 15 and 30 nucleotides, preferably between 18 and 22nucleotides and most preferably 19 and 21 nucleotides; and / or(ii) Probe 5 has a Tm of between 59°C and 71°C, preferably between 60°C and 70°C, morepreferably between 63°C and 67°C; and / or (iii) Probe 5 comprises or consists of a nucleic acid sequence of SEQ ID NO: 106; and / or(iv) Probe 5 comprises one or more locked nucleic acids (LNA) and / or a minor grove binding(MGB) moiety; and / or (v) Probe 5 comprises a detectable label.

21. The method according to any one of claims 17 to 20, wherein:(i) the PCR is qPCR, dPCR, ddPCR or cdPCR; and / or(ii) the PCR uses an annealing temperature of between 55°C and 65°C, preferably between58°C and 60°C; and / or (iii) the PCR comprises an activation step and / or a degradation step; and / or(iv) annealing and elongation are performed at the same temperature; and / or(v) the PCR comprises between 40 and 50 cycles of denaturation and annealing / elongation, preferably 45 cycles.

22. The method according to any one of claims 17 to 21, wherein the reaction mixture furthercomprises an internal positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 68 or 112 or 115.

23. The method according to claim 22, wherein the internal positive control nucleic acid sequencecomprises or consists of a nucleic acid sequence at least 90% identical to the nucleic acid sequence of SEQ ID NO: 68 or 112 or 115, or its reverse complement.

24. The method according to any one of claims 17 to 23, wherein the reaction mixture furthercomprises a discriminatory positive control nucleic acid sequence comprising at least 18 consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 109 and at least 18consecutive nucleic acids of the nucleic acid sequence of SEQ ID NO: 110 and between thesetwo nucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides, wherein the reaction mixture preferably further comprises at least a third nucleic acid probe (Probe 3) and / or a fourth nucleic acid probe (Probe 4) annealing to the intervening nucleic acid sequence or to its reverse complement at a sequence that is different from thesequence to which Probe 5 anneals.

25. The method according to claim 24, whereina) Probe 3: (ai) has a length between 20 and 42 nucleotides, preferably between 21 and 30 nucleotides andmost preferably 22 and 24 nucleotides; and / or (aii) has a Tm of between 55°C and 70°C, preferably between 58°C and 69°C, more preferablybetween 59°C and 68°C; and / or (aiii) comprises or consists of a nucleic acid sequence of SEQ ID NO: 69 or its reversecomplement; and / or (aiv)comprises one or more locked nucleic acids (LNA) and / or a minor grove binding (MGB) moiety; and / or (av) comprises a detectable label different from the label of Probe 4 and Probe 5;and / or b) Probe 4: (bi) has a length between 20 and 42 nucleotides, preferably between 21 and 30 nucleotides andmost preferably between 22 and 24 nucleotides; and / or (bii) has a Tm of between 55°C and 70°C, preferably between 58°C and 69°C, more preferablybetween 59°C and 68°C; and / or (biii) comprises or consists of a nucleic acid sequence of SEQ ID NO: 71 or its reversecomplement; and / or (biv) comprises one or more locked nucleic acids (LNA) and / or a minor grove binding (MGB) moiety; and / or (bv) comprises a detectable label different from the label of Probe 3 and Probe 5.

26. The method according to claim 24 or 25, wherein the discriminatory positive control nucleicacid sequence comprises or consists of a nucleic acid sequence at least 90% identical to thenucleic acid sequence of SEQ ID NO: 113 or its reverse complement.

27. The method according to any one of claims 17 to 26, wherein the sample is a biological samplepreferably selected from the group consisting of a cell bank, a culture medium, a cell culture, a cell culture supernatant, a medicinal product, a vaccine preparation, blood, saliva, and sputum.

28. A pair of primers for detecting MMV in a sample comprising: a primer P3 annealing to thereverse complement of a nucleic acid sequence of SEQ ID NO: 109, and a primer P4 annealingto a nucleic acid sequence of SEQ ID NO: 110.

29. A kit for detecting MMV in a sample, wherein the kit comprises the pair of primers of claim 28and a nucleic acid probe (Probe 5) annealing to a nucleic acid sequence of SEQ ID NO: 111 orits reverse complement, preferably wherein the kit further comprises one or more of:(i) a PCR reaction mixture;(ii) an internal positive control nucleic acid sequence comprising at least 18 consecutivenucleic acids of the nucleic acid sequence of SEQ ID NO: 109 and at least 18 consecutivenucleic acids of the nucleic acid sequence of SEQ ID NO: 110 and between these twonucleic acid sequences an intervening nucleic acid sequence of a length of at least 18 nucleotides; (iii) a discriminatory positive control nucleic acid sequence comprising at least 18 consecutivenucleic acids of the nucleic acid sequence of SEQ ID NO: 109 and at least 18 consecutivenucleic acids of the nucleic acid sequence of SEQ ID NO: 110 and between these twonucleic acid sequences an intervening nucleic acid sequence of a length of at least 29 nucleotides, wherein the intervening nucleic acid sequence preferably does not differ from SEQ ID NO: 111 so that Probe 5 is capable of annealing to the intervening nucleic acidsequence; (iv) means for extracting and / or purifying DNA from the sample; and(v) instructions for performing PCR with the primers.

30. The method according to any one of claims 17 to 27, the pair of primers according to claim 28or the kit according to claim 29, wherein the virus selected from the group consisting ofAnelloviridae, Inoviridae, Parvoviridae, preferably Parvovirus, Erythovirus, Dependovirus,Amdovirus and Bocavirus, more preferably Parvovirus, and most preferably Mouse Minute Virus.