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应用高速实时 RT-PCR 快速检测口蹄疫病毒、甲型流感病毒和经典猪瘟病毒。

Rapid detection of foot-and-mouth disease virus, influenza A virus and classical swine fever virus by high-speed real-time RT-PCR.

机构信息

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Suedufer 10, 17493 Greifswald-Insel Riems, Germany.

出版信息

J Virol Methods. 2013 Oct;193(1):50-4. doi: 10.1016/j.jviromet.2013.05.005. Epub 2013 May 20.

Abstract

High sensitivity, minor risk of cross-contamination and in particular the rapid reaction time make quantitative real-time polymerase chain reaction (qPCR) assays well suited for outbreak investigations as well as for monitoring epidemics of pathogens. In this study qPCR assays for three highly contagious animal diseases, namely foot-and-mouth-disease (FMD), influenza A (IA) and classical swine fever (CSF) have been developed. Furthermore, an amplification control targeting 18S ribosomal RNA was included. Each assay was validated with samples from infected animals using three different standard qPCR-machines in two thermal profiles: one standard and one high-speed approach, respectively. The high-speed PCR assays allowed the reliable diagnosis of FMD, influenza A and CSF in less than 28 min with an analytical sensitivity of at least 200 genome copies/μl in every case, with slight differences regarding reaction time and sensitivity for the individual PCR-cycler instruments. Therefore, the newly established rapid RT-PCR systems will be a valuable method for the monitoring and control of these three important viruses and will be a robust option for the development of novel molecular pen-side tests.

摘要

高灵敏度、交叉污染风险小,特别是反应时间快,这些使得定量实时聚合酶链反应(qPCR)检测非常适合暴发调查以及对病原体流行情况的监测。在这项研究中,我们开发了针对三种高传染性动物疾病的 qPCR 检测方法,即口蹄疫(FMD)、甲型流感(IA)和经典猪瘟(CSF)。此外,还包括了针对 18S 核糖体 RNA 的扩增对照。我们使用来自感染动物的样本,在两种热曲线(一种标准,一种高速)下,使用三种不同的标准 qPCR 仪器对每种检测方法进行了验证。在每种情况下,高速 PCR 检测方法都能在不到 28 分钟的时间内可靠地诊断 FMD、IA 和 CSF,其分析灵敏度至少为 200 个基因组拷贝/μl,对于不同的 PCR 循环仪,反应时间和灵敏度略有差异。因此,新建立的快速 RT-PCR 系统将是监测和控制这三种重要病毒的有效方法,并且是开发新型分子笔式检测的可靠选择。

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