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52 results about "Sprivivirus" patented technology

Sprivivirus is a genus of viruses in the family Rhabdoviridae, order Mononegavirales. Fish serve as natural hosts.

Antisense antiviral compound and method for treating ssRNA viral infection

The invention provides antisense antiviral compounds and methods of their use and production in inhibition of growth of viruses of the Flaviviridae, Picomoviridae, Caliciviridae, Togaviridae, Arteriviridae, Coronaviridae, Astroviridae and Hepeviridae families in the treatment of a viral infection. The antisense antiviral compounds are substantially uncharged morpholino oligonucleotides having a sequence of 1240 subunits, including at least 12 subunits having a targeting sequence that is complementary to a region associated with stem-loop secondary structure within the 5′-terminal end 40 bases of the positive-sense RNA strand of the virus.
Owner:AVI BIOPHARMA

Vectors with modified initiation codon for the translation of aav-rep78 useful for production of aav

The present invention relates nucleic acid constructs for the production of recombinant parvoviral (e.g. adeno-associated viral) vectors in insect cells, to insect cells comprising such constructs and to methods wherein the cells are used to produce recombinant parvoviral virions. The insect cells preferably comprise a first nucleotide sequence encoding the parvoviral rep proteins whereby the initiation codon for translation of the parvoviral Rep78 protein is a suboptimal initiation codon that effects partial exon skipping upon expression in insect cells. The insect cell further comprises a second nucleotide sequence comprising at least one parvoviral (AAV) inverted terminal repeat (ITR) nucleotide sequence and a third nucleotide sequence comprising a sequences coding for the parvoviral capsid proteins.
Owner:UNIQURE IP BV

Methods for real-time multiplex isothermal detection and identification of bacterial, viral, and protozoan nucleic acids

Herein disclosed are rapid real-time isothermal multiplex methods of detecting, identifying and quantifying bacterial, viral, and protozoan nucleic acids in a sample. These include contacting the sample with two or more sets of pathogen-specific reverse transcription loop-mediated isothermal amplification primers and novel oligofluorophores specific for the target bacterial, viral, and parasitic nucleic acids of interest such as human immunodeficiency virus, Ebola virus, Marburg virus, Yellow fever virus, hepatitis-B virus, Lassa fever virus, Plasmodium, hepatitis-C virus, hepatitis-E virus, dengue virus, Chikungunya virus, Japanese Encephalitis virus, Middle Eastern Respiratory Syndrome Corona virus, Mycobacterium, West Nile virus, Cytomegalovirus, Parvovirus, Leishmania, Trypanosoma, and Zika virus nucleic acids, under conditions sufficient to produce detectable real-time amplification signals in about 10 to 40 minutes. The amplification signals are produced by pathogen-specific fluorogenic labels included in one or more of the primers. Also, novel reaction and sample lysis buffers, primers, and kits for rapid multiplex detection, quantification, and identification of bacterial, viral, and protozoan nucleic acids by real-time isothermal amplification are herein disclosed.
Owner:NYAN DOUGBEH CHRIS

Multiple real-time quantitative PCR primer, probe and detection method for identifying viral pathogens relevant to fever with eruption syndrome as infection diseases

The invention discloses multiple real-time quantitative PCR primer, probe and a detection method for identifying viral pathogens relevant to fevers with eruption syndromes as infection diseases, which is used for carrying out multiple real-time fluorescent quantitative PCR detection on varicella-herpes zoster viruses, human small DNA (Deoxyribonucleic Acid) viruses B19, enteroviruses (enteroviruses 71 type and coxsackie viruses A16 type), dengue viruses, rubella viruses and measles viruses. The invention can simultaneously carry out qualitative or quantitative detection on eight kinds of human viruses in various types of samples by multiple double-tubes PCR. The detection method has the advantages of simple operation, short time consumption, high sensitivity and strong specificity, is suitable for field detection, early diagnosis, epidemics detection and research and the like, and takes the actions of assistance and identification diagnosis on the fevers with eruption syndromes.
Owner:SUN YAT SEN UNIV

Fluorescent quantitative primer group for visual differential diagnosis of waterfowl parvoviruses

The invention discloses a real-time fluorescent quantitative PCR (Polymerase Chain Reaction) primer group for visual detection on infection conditions of goose parvovirus (GPV) and muscovy duck parvovirus (MDPV) and a method thereof. According to the method, the detection on the infection conditions of GPV and MDPV is carried out by using dissolution curve temperature difference caused by the difference between nucleotide GC contents of GPV and MDPV specific gene fragment regions amplified by primers, and the infection conditions of GPV and MDPV can be subjected to visual differential diagnosis specifically by only combining the SYBR Green I based real-time fluorescent quantitative PCR primer group to dissolution curves which are automatically generated after reaction is ended. The method disclosed by the invention is simple and is relatively high in efficiency and accuracy.
Owner:INST OF ANIMAL HUSBANDRY & VETERINARY FUJIAN ACADEMY OF AGRI SCI

Pelodiscus sinensis picornavirus complete genome sequence and applications thereof

The invention relates to a separated nucleic acid molecule having a nucleotide sequence shown as SEQ ID NO:1 or an antisense sequence of the SEQ ID NO:1. The nucleic acid molecule is derived from pelodiscus sinensis picornavirus strain CNSR2011. The nucleic acid molecule can be used for preparing primers, probes or kits, wherein the primers, the probes and the kits are used for detecting the pelodiscus sinensis picornavirus. The nucleic acid molecule can also be used for preparing a vaccine of the pelodiscus sinensis picornavirus, and an anti-pelodiscus sinensis picornavirus antibody.
Owner:ZHEJIANG INST OF FRESH WATER FISHERIES

Strains, application of strains, vaccine and preparation method of vaccine

InactiveCN105713855AReduce stress responseReduced immunization workloadAntibacterial agentsBacteriaAntigenMink enteritis
The invention relates to the field of biotechnology, in particular to strains, application of the strains, a vaccine and a preparation method of the vaccine, and provides a combined inactivated vaccine for mink parvoviral enteritis and hemorrhagic pneumonia and a preparation process of the combined inactivated vaccine. The (bacterium) virus strains of the vaccine include the mink enteritis parvovirus strain (MEVB strain) and the mink pseudomonas aeruginosa G-type DL15 strain, B-type JL08 strain, C-type WD01 strain, I-type WF05 strain and F-type DL03 strain which are popular in China. The parvoviral enteritis strain and the pseudomonas aeruginosa strains serving as antigens are cultured, inactivated with formaldehyde and then mixed in proportion, aluminium hydroxide colloid is added in proportion, and the vaccine is prepared. The immunity period of the vaccine is 6 months, the immunity protection rate is 80% or above, and the vaccine can be used for preventing mink parvoviral enteritis and mink hemorrhagic pneumonia at the same time, reduces the immunization workload of raising households and the stress response of minks and has good market application prospects.
Owner:INST OF SPECIAL ANIMAL & PLANT SCI OF CAAS

Low odor, hard surface sporicides and chemical decontaminants

A low odor, liquid disinfectant composition comprising multiple components, which, upon mixing, provide an aqueous solution comprising low levels of peracetic acid for use in decontaminating articles and surfaces contaminated with bacteria, viruses, fungi and other chemical and biological contaminants including, but not limited to, spores, such as Clostridium difficile (C. diff), Clostridium sporogenes, and anthrax, mouse parvo virus, and mustard, nerve and other chemical and biological warfare agents. The disinfectant composition is prepared just prior to use by combining two or more separately packaged components, one component which is an acetyl donor comprising TAED or DAMA, and the other component which is a hydrogen peroxide solution.
Owner:AMERICAN STERILIZER CO

Mink canine parvovirus enteritis pathogen antigen colloidal gold detection test strip and production method thereof

The invention discloses a mink canine parvovirus enteritis pathogen antigen colloidal gold detection test strip and a production method thereof, and relates to the technical field of detection of fur animal viral infectious disease pathogens. The colloidal gold detection test strip comprises a sample pad, a colloidal gold pad, an NC film and an absorption pad, the detection line of the NC film is sprayed with a VP2 protein, and the quality control line of the NC film is sprayed with a goat-anti-mouse second antibody. The production method of the mink canine parvovirus enteritis pathogen antigen colloidal gold detection test strip mainly comprises the following steps: carrying out prokaryotic expression to obtain mink parvovirus (MEV) VP2 and VP1 proteins, and purifying the proteins; preparing an MEV monoclonal antibody; preparing a colloidal gold solution; preparing a colloidal gold antibody solution; preparing the colloidal gold pad; preprocessing the NC film; and assembling. The test strip is helpful for purifying the mink canine parvovirus enteritis in fur animal culturing farms, and is convenient for basic veterinary personnel to operate.
Owner:INST OF SPECIAL ANIMAL & PLANT SCI OF CAAS

Virus DNA (deoxyribonucleic acid) and RNA (ribonucleic acid) co-extraction kit and extraction method

The invention relates to a virus DNA and RNA co-extraction kit and an extraction method, and belongs to the technical field of biology. By matching the lysate, the rinsing liquid and other solutions with the extraction method, the method can directly extract viral nucleic acids (DNA and RNA) in cell-free body fluids of human and animals, such as centrifugal supernatant of serum, plasma and tissue grinding fluid. According to the method and the kit, DNA and RNA can be extracted at the same time, operation is easy, particularly, the nucleic acid extraction sensitivity of the small viruses is high, and the extraction effect is better.
Owner:TIANJIN MOGENETICS BIOTECH CO LTD

Application of diacerein in preparation of antiviral drugs and treatment of virus infection

The invention discloses application of diacerein in preparation of antiviral drugs and treatment of virus infection, and belongs to new application of diacerein. The experimental results prove that diacerein can be used for effectively inhibiting hepatophilic DNA viruses, retroviruses, enteroviruses, orthomyxoviruses, fibroviruses, reoviruses, arenavirus, hepatitis E viruses, astroviruses, circoviruses, coronaviruses, parvoviruses, adenoviruses, polyomaviruses, herpes viruses, poxviruses, human papillomaviruses, paramyxoviruses, flaviviruses, herpes viruses, alphaviruses and rhabdoviruses.
Owner:CHINA INSPECTION SCI PHARM BEIJING GRP CO LTD

Primer, probe and kit for specifically detecting type-3 ungulata bocaviruses parvovirus

The invention discloses a primer, a probe and a kit for specifically detecting type-3 ungulata bocaviruses parvovirus. The detection kit and the detection agent disclosed by the invention have the advantages of detection accuracy, high sensitivity, high specificity, simplicity, convenience and rapidness and is good in detection property.
Owner:中华人民共和国惠州出入境检验检疫局

Bovine parvovirus type I and type II RPA (recombinase polymerase amplification) detection kit and detection method thereof

The invention belongs to the technical field of in-vitro detection, and particularly relates to a bovine parvovirus type I and type II RPA (recombinase polymerase amplification) detection kit and a detection method thereof. The kit provided by the invention comprises a dual RPA reaction system and RPA Basic freeze-dried powder containing recombinase. The dual RPA reaction system comprises a DNA (Deoxyribose Nucleic Acid) template of the virus, an upstream primer pair, a downstream primer pair, a Rehydration Buffer and magnesium acetate tetrahydrate. The kit reacts for 20 minutes at the temperature of 45 DEG C, and an obtained product is subjected to agarose electrophoresis detection. According to the invention, the upstream primer, the downstream primer and the reaction time are screened, so that the bovine parvovirus type I and the bovine parvovirus type II are simultaneously detected, and the problems of long time consumption, high detection limit and dependence on professional equipment and professionals in bovine parvovirus detection are solved. The invention provides an efficient and accurate solution for large-scale bovine parvovirus screening, and has a good application prospect.
Owner:HENAN UNIV OF SCI & TECH

Primer pair and kit for detecting duck parvovirus and duck dependovirus universal type

The present application relates to a kind of primer pair for detecting duck parvovirus and duck dependent virus universal type and its kit and detection method.The kit includes four duck parvovirus (MDPV, N-MDPV, GPV and N-GPV) and the primer pair of duck dependent virus (DAAV) universal type newly found in recent years, sequence as shown in SEQ ID NO.1-2.The specific primer used in the present application can effectively amplify four duck parvovirus (MDPV, N-MDPV, GPV and N-GPV) and the duck dependent virus (DAAV) newly found in recent years, and can quickly determine whether the above pathogen infection exists in the sample to be tested.Currently, there is no duck parvovirus and duck dependent virus (both belong to parvovirus family parvovirus subfamily dependent parvovirus genus) universal type detection kit related research report at home and abroad, and the establishment of the present application can fill the gap in related fields at home and abroad.
Owner:INST OF ANIMAL HUSBANDRY & VETERINARY FUJIAN ACADEMY OF AGRI SCI

Quadruple TaqMan real-time fluorescent quantitative PCR primer group and probe group for simultaneously detecting cGPV, MDPV, MDGPV and SBDSV and kit thereof

The invention relates to a quadruple TaqMan real-time fluorescent quantitative PCR (Polymerase Chain Reaction) primer group and a probe group for simultaneously detecting cGPV (Complementary Glutathione Virus), MDPV (Minimal Disease Papilloma Virus), MDGPV (Minimal Disease Papilloma Virus) and SBDSV (Sequence Broadcast DSV) and a kit thereof. The sequences of the primer group and the probe group are respectively shown as SEQ ID NO.1-12. The research successfully develops and verifies a multiple TaqMan-MGB real-time fluorescent PCR method capable of simultaneously detecting and distinguishing four important waterfowl parvoviruses (cGPV, MDPV, MDGPV and SBDSV). The method has good specificity, repeatability and high sensitivity. Compared with a conventional PCR method, the multiple detection method has the advantages that the clinical waterfowl parvovirus detection rate is remarkably improved, mixed infection can be effectively recognized, and the clinical diagnosis efficiency is greatly improved.
Owner:INST OF ANIMAL HUSBANDRY & VETERINARY FUJIAN ACADEMY OF AGRI SCI

A 48e-scfv-fc recombinant antibody with broad-spectrum activity against waterfowl parvovirus and a preparation method and application thereof

PendingCN122628220APassive ImmunizationsAntigen epitope
The present application relates to a 48E-scFv-Fc recombinant antibody with broad-spectrum activity against waterfowl parvovirus, a construction method and application thereof, the 48E-scFv-Fc recombinant antibody comprising a light chain variable region and a heavy chain variable region, and the amino acid sequences of the light chain variable region and the heavy chain variable region are shown as SEQ ID NO: 1-2. The present application provides a coding gene for encoding the recombinant antibody, which comprises a DNA sequence shown as SEQ ID NO: 3-4. The present application also provides a corresponding recombinant plasmid and a preparation method of the 48E-scFv-Fc recombinant antibody, etc. The 48E-scFv-Fc recombinant antibody can simultaneously recognize four waterfowl parvoviruses of cGPV, MDPV, MDGPV and SBDSV, and has a good application prospect in immunological detection of waterfowl parvovirus infection, antigen epitope research, passive immunization preparation development and broad-spectrum antibody drug research, etc.
Owner:INST OF ANIMAL HUSBANDRY & VETERINARY FUJIAN ACADEMY OF AGRI SCI

Variable cleavage polypeptides and uses thereof

The invention provides a variable cleavage polypeptide and application thereof, the variable cleavage polypeptide is a polypeptide composed of 23 amino acids at the N terminal of calendula spica HBFD, and can realize specific cleavage in tobacco and multi-protein tandem expression of a single expression cassette. The cleavage specificity of the variable cleavage polypeptide in plants is superior to that of a previously reported small RNA virus 2A self-cleavage polypeptide, and reduction of non-specific cleavage is facilitated. The variable cleavage polypeptide is a protein cleavage element derived from a plant, and the application value of a multi-protein tandem expression technology based on a single expression cassette in a plant bioreactor is improved.
Owner:TOBACCO RESEARCH INSTITUTE OF CHINESE ACADEMY OF AGRICULTURAL SCIENCES (QINGZHOU TOBACCO RESEARCH INSTITUTE OF CHINA NATIONAL TOBACCO COMPANY)

A virus DNA, RNA co-extraction kit and extraction method

The present application relates to a kit and method for the co-extraction of viral DNA and RNA, and belongs to the field of biotechnology. The present invention can directly extract viral nucleic acids (DNA and RNA) from cell-free body fluids of humans and animals, such as serum, plasma, and centrifugal supernatants of tissue grinding fluid, by combining solutions such as lysate and rinse solution with extraction methods. The method and kit of the present invention can simultaneously extract DNA and RNA, and are simple to operate, especially for small virus nucleic acid extraction with high sensitivity and better extraction effect.
Owner:TIANJIN MOGENETICS BIOTECH CO LTD

Multiple real-time quantitative PCR primer, probe and detection method for identifying viral pathogens relevant to fever with eruption syndrome as infection diseases

The invention discloses multiple real-time quantitative PCR primer, probe and a detection method for identifying viral pathogens relevant to fevers with eruption syndromes as infection diseases, which is used for carrying out multiple real-time fluorescent quantitative PCR detection on varicella-herpes zoster viruses, human small DNA (Deoxyribonucleic Acid) viruses B19, enteroviruses (enteroviruses 71 type and coxsackie viruses A16 type), dengue viruses, rubella viruses and measles viruses. The invention can simultaneously carry out qualitative or quantitative detection on eight kinds of human viruses in various types of samples by multiple double-tubes PCR. The detection method has the advantages of simple operation, short time consumption, high sensitivity and strong specificity, is suitable for field detection, early diagnosis, epidemics detection and research and the like, and takes the actions of assistance and identification diagnosis on the fevers with eruption syndromes.
Owner:SUN YAT SEN UNIV

Fusion protein 210 and its use in optimizing viral replication

The invention provides fusion protein 210 and applications thereof in virus replication optimization. The fusion protein 210 is a truncated part of P60 protein, preserves a function for promoting replication of a plurality of viruses of the P60, and does not generate toxicity on cells in an effective concentration range. The fusion protein 210 can increase the virus titer by two orders of magnitudes in a wide-spectrum range (0.0001-0.1 MOI), and therefore virus identification and detection can be facilitated, rhabdovirus VSV, flaviviridae HCV, parvoviridae EV71, and the like can be detected, and time for detection is shortened by 50% or less. The fusion protein 210 obtained by a prokaryotic expression system is high in expression efficiency and easy to purify, the one-step purification efficiency can be 85% or above, and the protein final concentration can be 3 mg / mL. Accordingly, through directly adding the fusion protein 210 into a virus culture medium, a plurality of virus isolate strains can be detected under low titer conditions, and operation is simple, convenient and rapid. The fusion protein 210 has important influences and significance in the fields of production, learning, researching, and the like of the virology.
Owner:CHINA AGRI UNIV

Fusion protein 210 and applications thereof in virus replication optimization

The invention provides fusion protein 210 and applications thereof in virus replication optimization. The fusion protein 210 is a truncated part of P60 protein, preserves a function for promoting replication of a plurality of viruses of the P60, and does not generate toxicity on cells in an effective concentration range. The fusion protein 210 can increase the virus titer by two orders of magnitudes in a wide-spectrum range (0.0001-0.1 MOI), and therefore virus identification and detection can be facilitated, rhabdovirus VSV, flaviviridae HCV, parvoviridae EV71, and the like can be detected, and time for detection is shortened by 50% or less. The fusion protein 210 obtained by a prokaryotic expression system is high in expression efficiency and easy to purify, the one-step purification efficiency can be 85% or above, and the protein final concentration can be 3 mg / mL. Accordingly, through directly adding the fusion protein 210 into a virus culture medium, a plurality of virus isolate strains can be detected under low titer conditions, and operation is simple, convenient and rapid. The fusion protein 210 has important influences and significance in the fields of production, learning, researching, and the like of the virology.
Owner:CHINA AGRI UNIV

Small RNA (Ribonucleic Acid) virus gene of white foot shrimp and application of small RNA virus gene

The invention discloses a gene of a small RNA (Ribonucleic Acid) virus of white foot shrimps and application of the gene. On the basis of the small RNA virus gene of the white foot shrimp, the nested and fluorescent quantitative PCR detection method of the small RNA virus of the white foot shrimp is established. The established nested PCR method and fluorescent quantitative PCR method are high in sensitivity and good in repeatability and specificity, the lowest detection limit is 10 copies / microliter, and the nested PCR method and the fluorescent quantitative PCR method can be used for screening non-toxic seed shrimps or shrimp seeds and are suitable for being popularized and used in base-level culture units of freshwater shrimps.
Owner:SUN YAT SEN UNIV

A real-time fluorescence quantitative PCR detection method for Ailurus fulgens parvovirus

The present invention belongs to the technical field of virus detection, and particularly relates to a real-time fluorescence quantitative PCR detection method for red panda parvovirus. According to the gene sequence of RPAV VP1, the present invention designs and synthesizes specific primers, constructs a recombinant plasmid pcDNA3.1HA-RPAV-VP1, establishes a standard curve using it as a standard product, constructs a real-time fluorescence quantitative PCR detection system for red panda parvovirus, and realizes specific detection of RPAV. It can detect recombinant plasmids at 10<supgt;1< / supgt; copies / μL. It has the advantages of high specificity and sensitivity, good repeatability and short time consumption. The detection results can be directly read out through computer software, simplifying the experimental steps and saving detection time. It provides a new detection method for detecting red panda parvovirus, makes up for the technical blank in the detection of panda parvovirus, provides a basis for diagnosing red panda parvovirus infection, and plays an important role in protecting red pandas and giant pandas.
Owner:JIANGSU UNIV +1

Parvoviral vectors and methods of making and use thereof

A recombination parvovirus vector that comprises a parvovirus capsid and a double-stranded vector genome having a sense-strand and an antisense-strand. The sense-strand comprises in the 5' to 3' direction: a parvovirus terminal repeat at the 5' end a coding sequence of a gene of interest (GOI); and a parvovirus terminal repeat at the 3' end. The vector genome further comprises a RNA destabilization / destruction domain (RDDD).
Owner:耐克基因有限责任公司

Multiplex fluorescent quantitative PCR (polymerase chain reaction) detection reagent for synchronously detecting four DNA (deoxyribonucleic acid) viruses related to infectious infertility

The invention discloses a multiplex fluorescent quantitative PCR (Polymerase Chain Reaction) detection reagent for synchronously detecting four DNA (Deoxyribose Nucleic Acid) viruses related to infectious infertility. The detection reagent comprises specific primers and probes aiming at human microviruses, adenoviruses, polyoma viruses and adeno-associated viruses; the multiple fluorescence detection method used in the invention not only can synchronously detect four infectious DNA viruses in a single reaction tube, but also can simultaneously measure the load of the viruses, and has great value for researching infectious clinical diseases. The reagent disclosed by the invention has the characteristics of strong specificity, high sensitivity, good stability, simplicity in operation, less time consumption and the like, and can greatly improve the detection efficiency and reduce the detection cost when the method is used for performing large-scale clinical screening on the infection of the four viruses; meanwhile, the detection result can also provide important reference for formulating an individualized treatment scheme, so that the kit has important clinical application value and social significance for realizing symptomatic medication and improving the treatment effect.
Owner:KUNMING UNIV OF SCI & TECH

Human parvovirus: humink parvovirus

Provided herein are sequences of the genomes and encoded proteins of a new human parvovirus, Humink parvovirus, and variants thereof. Also provided are methods of detecting the Humink parvovirus and diagnosing Humink parvovirus infection, methods of treating or preventing Humink parvovirus infection, and methods for identifying anti-Humink parvovirus compounds.
Owner:BLOOD SYST INC

AAV-mediated expression using a synthetic promoter and enhancer

An isolated recombinant parvovirus vector comprising a synthetic enhancer comprising plurality of enhancer sequences operably linked to a promoter, and methods of using the vector, are provided.
Owner:THE UNIVERSITY OF IOWA RESEARCH

Primer and TaqMan-MGB probe group for fluorescent quantitative PCR (Polymerase Chain Reaction) detection of virulent and attenuated strains of classical waterfowl parvovirus

PendingCN121592809AMicrobiological testing/measurementMicroorganism based processesMgb probeMuscovy duck parvovirus
The invention relates to a primer and a TaqMan-MGB probe group for fluorescent quantitative PCR (Polymerase Chain Reaction) detection of virulent and attenuated strains of classical waterfowl parvovirus, the primer and the TaqMan-MGB probe group comprise a fluorescent quantitative PCR detection primer and a probe group for virulent and attenuated strains of goose parvovirus respectively, and the sequences of the primer and the probe group are shown as SEQ ID NO.1-5 respectively; the primer and the TaqMan-MGB probe group further comprise a fluorescent quantitative PCR detection primer and a probe group for virulent and attenuated muscovy duck parvovirus respectively, and the sequences of the primer and the probe group are shown as SEQ ID NO.6-9 respectively. According to the invention, through systematic test verification and reaction condition optimization, an optimal primer-probe combination is screened out, a GPV TaqMan-MGB dual fluorescent quantitative PCR detection method and an MDPV TaqMan dual fluorescent quantitative PCR detection method are respectively and successfully established, and the detection of virulent and attenuated classical waterfowl parvovirus is realized.
Owner:INST OF ANIMAL HUSBANDRY & VETERINARY FUJIAN ACADEMY OF AGRI SCI