首页> 外文期刊>Archives of Virology >Development of a molecular-beacon-based multi-allelic real-time RT-PCR assay for the detection of human coronavirus causing severe acute respiratory syndrome (SARS-CoV): a general methodology for detecting rapidly mutating viruses
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Development of a molecular-beacon-based multi-allelic real-time RT-PCR assay for the detection of human coronavirus causing severe acute respiratory syndrome (SARS-CoV): a general methodology for detecting rapidly mutating viruses

机译:基于分子信标的多等位基因实时RT-PCR检测方法的开发,用于检测引起严重急性呼吸综合征的人冠状病毒:SARS-CoV:一种检测快速变异病毒的通用方法

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摘要

Emerging infectious diseases have caused a global effort for development of fast and accurate detection techniques. The rapidly mutating nature of viruses presents a major difficulty, highlighting the need for specific detection of genetically diverse strains. One such infectious agent is SARS-associated coronavirus (SARS-CoV), which emerged in 2003. This study aimed to develop a real-time RT-PCR detection assay specific for SARS-CoV, taking into account its intrinsic polymorphic nature due to genetic drift and recombination and the possibility of continuous and multiple introductions of genetically non-identical strains into the human population, by using mismatch-tolerant molecular beacons designed to specifically detect the SARS-CoV S, E, M and N genes. These were applied in simple, reproducible duplex and multiplex real-time PCR assays on 25 post-mortem samples and constructed RNA controls, and they demonstrated high target detection ability and specificity. This assay can readily be adapted for detection of other emerging and rapidly mutating pathogens.
机译:新兴传染病已引起全球范围内对开发快速准确的检测技术的努力。病毒的快速突变性质带来了很大的困难,突显了对特异性检测遗传多样性菌株的需求。一种这样的传染病原体是SARS相关冠状病毒(SARS-CoV),该病毒于2003年出现。该研究旨在开发一种针对SARS-CoV的实时RT-PCR检测方法,考虑到其固有的遗传多态性通过使用耐错配的分子信标专门设计用于检测SARS-CoV S,E,M和N基因的耐错配分子信标,可以实现漂移和重组以及将遗传上不相同的菌株连续多次引入人类的可能性。将它们应用于25个验尸样品和构建的RNA对照品的简单,可重现的双链和多重实时PCR分析中,证明了其高靶标检测能力和特异性。该测定法可以很容易地适用于检测其他新兴和快速突变的病原体。

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