首页> 外文期刊>Journal of Virological Methods >Development of a minor groove binder assay for real-time one-step RT-PCR detection of swine vesicular disease virus.
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Development of a minor groove binder assay for real-time one-step RT-PCR detection of swine vesicular disease virus.

机译:小沟结合剂测定法的开发,用于实时实时一步RT-PCR检测猪水泡病病毒。

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The design and development of a 5' conjugated minor groove binder (MGB) probe real-time RT-PCR assay are described for rapid, sensitive and specific detection of swine vesicular disease virus (SVDV) RNA. The assay is designed to target the 2C gene of the SVDV genome and is capable of detecting 2x102 copies of an RNA standard per reaction. It does not detect any of the other RNA viruses that cause vesicular disease in pigs, or the human enterovirus, Coxsackie B5 virus (CVB5) which is closely related antigenically to SVDV. The linear range of this test was from 2x102 to 2x108 copies/ micro l. The assay is rapid and can detect SVDV RNA in just over 3.5 h including the time required for nucleic acid extraction. The development of this assay provides a useful tool for the differential diagnosis of SVD or for the detection of SVDV in research applications. This study demonstrates the suitability of MGB probes as a real-time PCR chemistry for the diagnosis of swine vesicular disease.Digital Object Identifier http://dx.doi.org/10.1016/j.jviromet.2010.11.001
机译:5'缀合的小沟结合剂(MGB)探针实时RT-PCR分析的设计和开发描述了快速,灵敏和特异地检测猪水泡病病毒(SVDV)RNA。该分析法旨在针对SVDV基因组的2C基因,并且能够在每个反应中检测2x10 2 个RNA标准品的拷贝。它没有检测到任何其他引起猪水泡病的RNA病毒,也没有检测到与SVDV在抗原上密切相关的人肠病毒柯萨奇B5病毒(CVB5)。此测试的线性范围是2x10 2 至2x10 8 拷贝/微升。该测定快速,可以在超过3.5小时的时间内检测到SVDV RNA,包括提取核酸所需的时间。该测定法的发展为研究应用中的SVD的鉴别诊断或SVDV的检测提供了有用的工具。这项研究证明了MGB探针作为实时PCR化学试剂诊断猪水疱病的适用性。数字对象标识符http://dx.doi.org/10.1016/j.jviromet.2010.11.001

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