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利用超高速定量实时 PCR 快速分型流感病毒。

Rapid typing of influenza viruses using super high-speed quantitative real-time PCR.

机构信息

Department of Molecular Medical Research, Tokyo Metropolitan Institute of Medical Science, 2-1-6, Kamikitazawa, Setagaya-ku, Tokyo 156-8506, Japan.

出版信息

J Virol Methods. 2011 Dec;178(1-2):75-81. doi: 10.1016/j.jviromet.2011.08.015. Epub 2011 Aug 22.

DOI:10.1016/j.jviromet.2011.08.015
PMID:21889540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7119501/
Abstract

The development of a rapid and sensitive system for detecting influenza viruses is a high priority for controlling future epidemics and pandemics. Quantitative real-time PCR is often used for detecting various kinds of viruses; however, it requires more than 2h per run. Detection assays were performed with super high-speed RT-PCR (SHRT-PCR) developed according to a newly designed heating system. The new method uses a high-speed reaction (18s/cycle; 40 cycles in less than 20min) for typing influenza viruses. The detection limit of SHRT-PCR was 1 copy/reaction and 10(-1) plaque-forming unit/reaction for viruses in culture supernatants during 20min. Using SHRT-PCR, 86 strains of influenza viruses isolated by the Tokyo Metropolitan Institute of Public Health were tested; the results showed 100% sensitivity and specificity for each influenza A and B virus, and swine-origin influenza virus. Twenty-seven swabs collected from the pharyngeal mucosa of outpatients were also tested, showing positive signs for influenza virus on an immunochromatographic assay; the results between SHRT-PCR and immunochromatography exhibited 100% agreement for both positive and negative results. The rapid reaction time and high sensitivity of SHRT-PCR makes this technique well suited for monitoring epidemics and pre-pandemic influenza outbreaks.

摘要

开发一种快速且灵敏的流感病毒检测系统对于控制未来的流感疫情和大流行至关重要。实时荧光定量 PCR 常用于检测各种病毒;然而,它每次运行需要 2 个多小时。根据新设计的加热系统,我们开发了超高速 RT-PCR(SHRT-PCR)来进行检测。该新方法采用高速反应(18s/循环;40 个循环不到 20 分钟)对流感病毒进行分型。SHRT-PCR 的检测限为 1 个拷贝/反应和 10(-1)个噬菌斑形成单位/反应,在 20 分钟内用于培养上清液中的病毒。使用 SHRT-PCR 对东京都公共卫生研究所分离的 86 株流感病毒进行了检测;结果表明,对于每一种甲型和乙型流感病毒以及猪源流感病毒,均具有 100%的敏感性和特异性。对 27 名门诊患者的咽拭子进行了检测,免疫层析检测呈流感病毒阳性;SHRT-PCR 与免疫层析的检测结果对于阳性和阴性结果均具有 100%的一致性。SHRT-PCR 的快速反应时间和高灵敏度使其非常适合用于监测流感疫情和大流行前的流感爆发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4ab/7119501/827579697d87/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4ab/7119501/235db93bb0be/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4ab/7119501/827579697d87/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4ab/7119501/235db93bb0be/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4ab/7119501/827579697d87/gr2.jpg

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