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Method for detecting infectious disease pathogens and kit

A technology for infectious diseases and pathogens, applied in the field of molecular biology, can solve the problem of not being able to detect multiple infectious disease pathogens at the same time, and achieve the effects of fast detection speed, stable results and strong specificity

Active Publication Date: 2009-09-30
海康生物科技(北京)有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The purpose of the present invention is to overcome the defect that the prior art cannot simultaneously detect multiple infectious disease pathogens, and provide a method for detecting infectious disease pathogens that may exist in biological samples, including:

Method used

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  • Method for detecting infectious disease pathogens and kit
  • Method for detecting infectious disease pathogens and kit
  • Method for detecting infectious disease pathogens and kit

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0063] Design and prepare primers and probe sequences.

[0064] According to the NCBI search, the specific gene sequences of Epstein-Barr virus, herpes simplex virus, cytomegalovirus, and adenovirus were selected, which are:

[0065] The EBNA-1 gene sequence of Epstein-Barr virus, GENEBANK accession number is U21205, selects the highly conserved part of sequence as target nucleic acid sequence, the target sequence that the present invention selects is EBNA-1 gene 161-308, and its nucleotide sequence is as SEQ ID NO. 1 shown;

[0066] The UL30 gene sequence of herpes simplex virus, the GENEBANK accession number is X14112, the target nucleic acid sequence selected in the present invention is 64208-64374 of the UL30 gene, and its nucleotide sequence is shown in SEQ ID NO.2;

[0067] The UL83 gene sequence of cytomegalovirus, the GENEBANK accession number is X17403, the target nucleic acid sequence selected in the present invention is 120206-120397 of the UL83 gene, and its nucle...

Embodiment 2

[0076] The kits described in the present invention are prepared. Composed of:

[0077] 1. Amplification system

[0078] Primers (4 groups) each group 10uM

[0079] Tris / HCl 10-100mM

[0080] Potassium chloride 1-10mM

[0081] BSA 1-5g / ml

[0082] Dithiothreitol 1-5mM

[0083] Nucleoside triphosphate and deoxynucleoside triphosphate equal concentration mixture 200-1000uM

[0084] Reverse transcriptase 5-300U

[0085] RNase H 5-300U

[0086] Phage T7 ribonucleic acid polymerase 5-300U

[0087] Negative control is RNase-free water

[0088] The positive control is 5pM artificially synthesized EBNA-1 gene sequence of Epstein-Barr virus, UL30 gene sequence of herpes simplex virus, UL83 gene sequence of cytomegalovirus, and coat protein hexamer gene sequence of adenovirus.

[0089] 2. Detection system

[0090] Detection probes (4 groups, all labeled with digoxin) 26μM

[0091] Capture probe (biotin-labeled) 26μM

[0092] Wash buffer 1 x TBS

[0093]Hybridization buffer ...

Embodiment 3

[0101] The method for detecting infectious disease pathogens that may exist in biological samples is also the method for using the kit of the present invention.

[0102] 1. Nucleic acid extraction

[0103] Take the sputum sample to be tested, centrifuge to get the supernatant, add 1ml guanidine isothiocyanate, mix well, then add 1ml TRIZOL, shake and mix well, and place in ice bath for 5 minutes. Add 350 ul of chloroform, vortex and mix well, and after static layering, immediately centrifuge at 12000 r / min for 20 minutes at 4°C. Transfer the supernatant to another centrifuge tube, add an equal volume of isopropanol (pre-cooled at 4°C) and mix well. Place at -20°C for 1 hour, centrifuge at 4°C and 12000r / min for 20 minutes, and precipitate the total RNA. Add 0.5ml of 75% ethanol to wash, centrifuge at 4°C and 12000r / min for 10 minutes, pour off the ethanol carefully, place at room temperature for 10 minutes, add An appropriate amount of DEPC-treated water was used to dissolve...

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Abstract

The invention discloses a method for detecting infectious disease pathogens possibly existing in a biological sample. The infectious disease pathogens comprise EB virus, herpes simplex virus, cytomegalic inclusion disease virus and adenovirus. The method comprises the following steps: expanding nucleic acid fragments of the biological sample, and detecting the nucleic acid fragments by using a probe. The invention also provides primers used for expanding and the probe used for detection. The invention also provides a kit comprising the primers. The method has the advantages of high sensitivity, strong specificity, simple operation and wide sample range, can simultaneously detect various infectious disease pathogens, and is suitable for early diagnosis of respiratory infectious diseases.

Description

technical field [0001] The invention relates to molecular biology, in particular to a method and a kit for detecting infectious disease pathogens. Background technique [0002] In the early stage of the epidemic of infectious diseases, accurate, fast and convenient detection of the pathogens of infectious diseases is the key to controlling the epidemic of infectious diseases. Although domestic and international surveillance systems for infectious diseases have been established, the existing detection methods have their own limitations. Serological tests detect pathogens by combining corresponding antibodies with antigens. This method is fast, simple, and easy to operate. It is suitable for early diagnosis of infectious diseases. [0003] The pathogen isolation method is to detect and identify pathogens by directly isolating and culturing pathogens. This method has high sensitivity and strong specificity, but the operation is complicated and time-consuming (it takes at lea...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/70C12Q1/68C12N15/11C12R1/93
Inventor 于常海刘乐庭冯晓燕
Owner 海康生物科技(北京)有限公司
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