Real-time fluorescence quantification PCR detection method for avian infectious laryngotracheitis virus

A real-time fluorescence quantitative, laryngotracheitis virus technology, applied in the field of molecular biology, can solve the problems of prone to false positives, PCR contamination, weak specificity, etc. Effect

Inactive Publication Date: 2017-08-29
HEBEI AGRICULTURAL UNIV.
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Problems solved by technology

[0004] The technical problem to be solved in the present invention is to provide a real-time fluorescence quantitative PCR detection method for chicken infectious laryngotracheitis virus in view of the deficiencies of the above-mentioned prior art, which solves the problem that traditional PCR methods are not specific, prone to false positives, and cumbersome to operate , easy to produce PCR pollution, can only semi-quantitative or qualitative analysis of the final product of the reaction, with strong specificity, high sensitivity, simple and fast operation, less prone to false positives, less likely to produce PCR pollution, and real-time detection of the PCR process , perform quantitative and qualitative analysis on each cycle, and the analysis results can be directly read out by the computer

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  • Real-time fluorescence quantification PCR detection method for avian infectious laryngotracheitis virus
  • Real-time fluorescence quantification PCR detection method for avian infectious laryngotracheitis virus
  • Real-time fluorescence quantification PCR detection method for avian infectious laryngotracheitis virus

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Embodiment 1

[0028] A real-time fluorescent quantitative PCR detection method for chicken infectious laryngotracheitis virus, comprising the steps of:

[0029] (1) Primer design: A pair of primers PF and PR were designed and synthesized for the gB gene of chicken infectious laryngotracheitis virus. The upstream primer PF is 5′-CAATGGCTTCGGAGAAAGAG-3′, and the downstream primer PR is 5′-GGCAATCCTGATCCCATCTA-3 ';

[0030] (2) Traditional PCR amplification: First, use the virus genome DNA extraction kit to extract ILTV DNA, and then perform PCR amplification. The PCR reaction system is: 2×mix 10 μL, upstream and downstream primers (25 μmol / μL) 0.5 μL, Template DNA 2μL, ddH 2 O Make up the volume to 20 μL. Reaction conditions: pre-denaturation at 94°C for 5 min; denaturation at 94°C for 30 s, annealing at 60°C for 30 s, extension at 72°C for 30 s, and 30 cycles; final extension at 72°C for 5 min, and then storage at 4°C. After the PCR products were subjected to 1.5% agarose gel electrophore...

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Abstract

The invention discloses a real-time fluorescence quantification PCR (real-time PCR) detection method for an avian infectious laryngotracheitis virus, relating to the molecular biology field. The real-time fluorescence quantification PCR detection method aims to the gB gene of the avian infectious laryngotracheitis virus to design and synthesize a pair of primers, namely PF: 5'-CAATGGCTTCGGAGAAAGAG-3' and PR: 5'-GGCAATCCTGATCCCATCTA-3'. By PCR amplification and standard product preparation, a fluorescence quantification PCR method for detecting the avian infectious laryngotracheitis virus is constructed; the specificity is stronger; the sensitivity is high; the operation is simple and fast; the real-time detection is performed on the PCR progress; the qualitative and quantitative analysis can be performed on each cycle; and the constructed fluorescence quantification PCR method for the avian infectious laryngotracheitis virus can be used for detecting the virus content in tissue.

Description

technical field [0001] The invention belongs to the field of molecular biology, and in particular relates to a detection method for chicken infectious laryngotracheitis virus. Background technique [0002] Infectious laryngotracheitis virus (ILTV) is a member of the herpesviridae family. The disease mainly affects poultry and can cause chicken infectious laryngotracheitis (AILT) is an acute, contact upper respiratory infectious disease. It is characterized by dyspnea, coughing, and expectoration of an exudate containing blood samples. During autopsy, swelling, hemorrhage and erosion of the larynx and tracheal mucosa can be seen. The case fatality rate is above 20%. After the disease was first reported in the United States in 1925, it has now spread to many chicken farming areas in the world. The disease spreads quickly and has a high mortality rate. It occurs and prevails in many areas in my country, endangering the development of the chicken industry. At present, there...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/70C12Q1/68
CPCC12Q1/701C12Q1/6851C12Q2563/107C12Q2545/114C12Q2561/113
Inventor 张铁陈谏王春光孟凡国张广群蒋桂娥贾书芬贾泽张石磊
Owner HEBEI AGRICULTURAL UNIV.
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