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{"title":"Poliovirus Replicon RNA Generation, Transfection, Packaging, and Quantitation of Replication","authors":"Ekaterina G. Viktorova, Sunil Khattar, Siba Samal, George A. Belov","doi":"10.1002/cpmc.47","DOIUrl":null,"url":null,"abstract":"<p>Poliovirus is a prototype member of the <i>Enterovirus</i> genus of the <i>Picornaviridae</i> family of small positive strand RNA viruses, which include important human and animal pathogens. Quantitative assessment of viral replication is very important for investigation of the virus biology and the development of anti-viral strategies. The poliovirus genome structure allows replacement of structural genes with a reporter protein, such as a luciferase or a fluorescent protein, whose signals can be detected and quantified <i>in vivo</i>, thus permitting observation of replication kinetics in live cells. This paper presents protocols for poliovirus replicon RNA production, purification, packaging and transfection, as well as techniques for monitoring <i>Renilla</i> luciferase replication signal in living cells. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.47","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpmc.47","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
Poliovirus is a prototype member of the Enterovirus genus of the Picornaviridae family of small positive strand RNA viruses, which include important human and animal pathogens. Quantitative assessment of viral replication is very important for investigation of the virus biology and the development of anti-viral strategies. The poliovirus genome structure allows replacement of structural genes with a reporter protein, such as a luciferase or a fluorescent protein, whose signals can be detected and quantified in vivo , thus permitting observation of replication kinetics in live cells. This paper presents protocols for poliovirus replicon RNA production, purification, packaging and transfection, as well as techniques for monitoring Renilla luciferase replication signal in living cells. © 2018 by John Wiley & Sons, Inc.
脊髓灰质炎病毒复制子RNA的产生、转染、包装和复制的定量
脊髓灰质炎病毒是小核糖核酸病毒科小正链RNA病毒家族肠病毒属的原型成员,包括重要的人类和动物病原体。病毒复制的定量评价对研究病毒生物学和制定抗病毒策略具有重要意义。脊髓灰质炎病毒的基因组结构允许用报告蛋白替代结构基因,如荧光素酶或荧光蛋白,其信号可以在体内检测和量化,从而可以观察活细胞中的复制动力学。本文介绍了脊髓灰质炎病毒复制子RNA的生产、纯化、包装和转染的方法,以及在活细胞中监测Renilla荧光素酶复制信号的技术。©2018 by John Wiley &儿子,Inc。
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