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简单、快速且经济高效:一种用于口蹄疫病毒基因组特征分析的通用逆转录聚合酶链反应(RT-PCR)及测序策略。

Simple, quick and cost-efficient: A universal RT-PCR and sequencing strategy for genomic characterisation of foot-and-mouth disease viruses.

作者信息

Dill V, Beer M, Hoffmann B

机构信息

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

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

出版信息

J Virol Methods. 2017 Aug;246:58-64. doi: 10.1016/j.jviromet.2017.04.007. Epub 2017 Apr 23.

Abstract

Foot-and-mouth disease (FMD) is a major contributor to poverty and food insecurity in Africa and Asia, and it is one of the biggest threats to agriculture in highly developed countries. As FMD is extremely contagious, strategies for its prevention, early detection, and the immediate characterisation of outbreak strains are of great importance. The generation of whole-genome sequences enables phylogenetic characterisation, the epidemiological tracing of virus transmission pathways and is supportive in disease control strategies. This study describes the development and validation of a rapid, universal and cost-efficient RT-PCR system to generate genome sequences of FMDV, reaching from the IRES to the end of the open reading frame. The method was evaluated using twelve different virus strains covering all seven serotypes of FMDV. Additionally, samples from experimentally infected animals were tested to mimic diagnostic field samples. All primer pairs showed a robust amplification with a high sensitivity for all serotypes. In summary, the described assay is suitable for the generation of FMDV sequences from all serotypes to allow immediate phylogenetic analysis, detailed genotyping and molecular epidemiology.

摘要

口蹄疫(FMD)是非洲和亚洲贫困与粮食不安全的主要成因之一,也是高度发达国家农业面临的最大威胁之一。由于口蹄疫具有极强的传染性,其预防、早期检测以及对疫情毒株进行即时特征分析的策略至关重要。全基因组序列的生成有助于进行系统发育特征分析、追踪病毒传播途径的流行病学情况,并对疾病控制策略提供支持。本研究描述了一种快速、通用且经济高效的逆转录聚合酶链反应(RT-PCR)系统的开发与验证,该系统用于生成口蹄疫病毒(FMDV)从内部核糖体进入位点(IRES)到开放阅读框末端的基因组序列。使用涵盖口蹄疫病毒所有七种血清型的十二种不同病毒株对该方法进行了评估。此外,还对来自实验感染动物的样本进行了检测,以模拟诊断现场样本。所有引物对均显示出对所有血清型的强劲扩增且具有高灵敏度。总之,所描述的检测方法适用于生成所有血清型的口蹄疫病毒序列,以便立即进行系统发育分析、详细的基因分型和分子流行病学研究。

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