SYBR Green I Real-time PCR method for quickly detecting and indentifying Hantaan virus infection

A fast technology for Hantaan virus, applied in the field of SYBR GreenⅠReal-time PCR, virology, immunology and immunology application, and molecular biology, can solve the problem that the specificity and sensitivity are not high enough, and it is not suitable for rapid on-site detection and separation Time-consuming and other problems of the identification method, to achieve the effect of simple and fast operation, good detection effect and strong contrast

A fast technology for Hantaan virus, applied in the field of SYBR GreenⅠReal-time PCR, virology, immunology and immunology application, and molecular biology, can solve the problem that the specificity and sensitivity are not high enough, and it is not suitable for rapid on-site detection and separation Time-consuming and other problems of the identification method, to achieve the effect of simple and fast operation, good detection effect and strong contrast

CN103436637BInactive Publication Date: 2015-05-20FOURTH MILITARY MEDICAL UNIVERSITY

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  • SYBR Green I Real-time PCR method for quickly detecting and indentifying Hantaan virus infection
  • SYBR Green I Real-time PCR method for quickly detecting and indentifying Hantaan virus infection
  • SYBR Green I Real-time PCR method for quickly detecting and indentifying Hantaan virus infection

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Embodiment Construction

[0030] 1. Design and synthesize a pair of real-time fluorescent quantitative PCR primers for Hantaan virus nucleic acid, provided by Beijing Aokeding

[0031] Sheng Biotechnology Co., Ltd. (Address: B206, No. 7, Fengxian Middle Road, Yongfeng Industrial Base, Haidian District, Beijing, Zip Code: 10094).

[0032] According to the S gene sequence of HTNV 76-118 strain (the accession number in GenBank is M14626.1), a pair of real-time fluorescent quantitative PCR primers for Hantaan virus nucleic acid were designed by using Oligo6.0 software and NCBI Blast analysis (see Table 1); Named respectively: upstream primer HTNV-F-13; downstream primer HTNV-R-13, the length of the amplified fragment is 144 bp.

[0033] Table 1. Primers designed for Hantaan virus

[0034]

[0035] The Hantaan virus nucleic acid is amplified by the above primers to accurately quantify the virus copy number in the sample. Total RNA from Vero E6 cells infected with HTNV 76-118 was extracted and reve...

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Abstract

The invention discloses a SYBR GreenⅠReal-time PCR method for rapid detection and identification of Hantaan virus infection. The method mainly designs a pair of specific primers based on the sequence of the conserved region of the S gene in the GenBank database. The gradient diluted positive plasmid was used as the standard, the reaction conditions were optimized, and the specific amplification by qRT-PCR was used to establish the SYBR Green Ⅰ Real-time PCR method for the detection of Hantaan virus nucleic acid in infected Vero E6 cells, infected mice and clinical patients, and the detection sensitivity A copy number of 101 was reached and tested for sensitivity, reproducibility, and specificity. Compared with conventional Hantaan virus detection and identification methods, this method has the advantages of rich types of detection specimens, wide application range, strong contrast, few operation steps, convenient and fast, high sensitivity, high repeatability and specificity, and has good The advantage of a linear relationship. It provides a strong experimental basis for the clinical, laboratory detection and epidemiological research of hemorrhagic fever with renal syndrome.

Description

technical field [0001] The invention belongs to the field of virus detection and relates to related fields such as molecular biology, virology, immunology and immune application. The invention specifically relates to a SYBR GreenⅠReal-time PCR method for rapid detection and identification of Hantaan virus infection. The samples for detection and identification of Hantaan virus nucleic acid include infection of Vero E6 cells, infection of experimental mice and clinical patients. It includes designing a pair of primers for specifically amplifying Hantaan virus, preparing standards, researching and optimizing experimental conditions, and performing qRT-PCR specificity on total RNA extracted from infected Vero E6 cells, infected experimental mice and clinical patient serum Amplification detection. Background technique [0002] Research status of diagnosis and detection of hemorrhagic fever with renal syndrome: [0003] Hantaan virus belongs to the genus Hantavirus in the Buny...

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Application Information

Patent Timeline
20 May 2015
Publication
CN103436637B
IPC
C12Q1/70; C12Q1/68; G01N21/64
Inventors
吴兴安; 刘梓谕