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用于测量沙粒病毒-细胞附着的高度灵敏检测方法。

Highly Sensitive Assay for Measurement of Arenavirus-cell Attachment.

作者信息

Klaus Joseph P, Botten Jason

机构信息

Department of Medicine, Division of Immunobiology, University of Vermont.

Department of Medicine, Division of Immunobiology, University of Vermont; Department of Microbiology & Molecular Genetics, University of Vermont;

出版信息

J Vis Exp. 2016 Mar 2(109):e53682. doi: 10.3791/53682.

Abstract

Arenaviruses are a family of enveloped RNA viruses that cause severe human disease. The first step in the arenavirus life cycle is attachment of viral particles to host cells. While virus-cell attachment can be measured through the use of virions labeled with biotin, radioactive isotopes, or fluorescent dyes, these approaches typically require high multiplicities of infection (MOI) to enable detection of bound virus. We describe a quantitative (q)RT-PCR-based assay that measures Junin virus strain Candid 1 attachment via quantitation of virion-packaged viral genomic RNA. This assay has several advantages including its extreme sensitivity and ability to measure attachment over a large dynamic range of MOIs without the need to purify or label input virus. Importantly, this approach can be easily tailored for use with other viruses through the use of virus-specific qRT-PCR reagents. Further, this assay can be modified to permit measurement of particle endocytosis and genome uncoating. In conclusion, we describe a simple, yet robust assay for highly sensitive measurement of arenavirus-cell attachment.

摘要

沙粒病毒是一类包膜RNA病毒,可导致严重的人类疾病。沙粒病毒生命周期的第一步是病毒颗粒附着于宿主细胞。虽然病毒与细胞的附着可以通过使用生物素、放射性同位素或荧光染料标记的病毒粒子来测量,但这些方法通常需要高感染复数(MOI)才能检测到结合的病毒。我们描述了一种基于定量(q)RT-PCR的检测方法,该方法通过定量病毒粒子包装的病毒基因组RNA来测量胡宁病毒Candid 1株的附着。该检测方法具有几个优点,包括极高的灵敏度以及能够在无需纯化或标记输入病毒的情况下,在很大的MOI动态范围内测量附着。重要的是,通过使用病毒特异性qRT-PCR试剂,这种方法可以很容易地调整以用于其他病毒。此外,该检测方法可以进行修改以允许测量颗粒内吞作用和基因组脱壳。总之,我们描述了一种简单而稳健的检测方法,用于高度灵敏地测量沙粒病毒与细胞的附着。

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