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用于研究丝状病毒进入机制的丝状病毒糖蛋白假型化水疱性口炎病毒的生产。

Production of Filovirus Glycoprotein-Pseudotyped Vesicular Stomatitis Virus for Study of Filovirus Entry Mechanisms.

作者信息

Brouillette Rachel B, Maury Wendy

机构信息

Department of Microbiology, University of Iowa, Iowa City, IA, USA.

出版信息

Methods Mol Biol. 2017;1628:53-63. doi: 10.1007/978-1-4939-7116-9_4.

Abstract

Members of the family Filoviridae are filamentous, enveloped, and nonsegmented negative-stranded RNA viruses that can cause severe hemorrhagic disease in humans and nonhuman primates with high mortality rates. Current efforts to analyze the structure and biology of these viruses as well as the development of antivirals have been hindered by the necessity of biosafety level 4 containment (BSL4). Here, we outline how to produce and work with Ebola virus glycoprotein bearing vesicular stomatitis virus (VSV) pseudovirions. These pseudovirions can be safely used to evaluate early steps of the filovirus life cycle without need for BSL4 containment. Virus gene expression in the transduced cells is easy to assess since the pseudovirions encode a reporter gene in place of the VSV G glycoprotein gene. Adoption of VSV for use as a pseudovirion system for filovirus GP has significantly expanded access for researchers to study specific aspects of the viral life cycle outside of BSL4 containment and has allowed substantial growth of filovirus research.

摘要

丝状病毒科的成员是丝状、包膜且不分节段的负链RNA病毒,可在人类和非人类灵长类动物中引起严重出血性疾病,死亡率很高。目前对这些病毒的结构和生物学进行分析以及开发抗病毒药物的工作因需要生物安全4级防护(BSL4)而受到阻碍。在此,我们概述了如何生产携带水泡性口炎病毒(VSV)假病毒的埃博拉病毒糖蛋白并对其进行操作。这些假病毒可安全用于评估丝状病毒生命周期的早期步骤,而无需BSL4防护。转导细胞中的病毒基因表达易于评估,因为假病毒编码一个报告基因来替代VSV G糖蛋白基因。采用VSV作为丝状病毒糖蛋白的假病毒系统,极大地扩展了研究人员在BSL4防护之外研究病毒生命周期特定方面的机会,并促进了丝状病毒研究的显著发展。

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