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一种用于持续性丙型肝炎病毒感染的细胞培养模型。

A Cell Culture Model for Persistent HCV Infection.

作者信息

Castro Victoria, Ávila-Pérez Ginés, Mingorance Lidia, Gastaminza Pablo

机构信息

Department of Molecular and Cellular Biology, Centro Nacional De Biotecnología-Consejo Superior de Investigaciones Científicas (CNB-CSIC), Madrid, Spain.

出版信息

Methods Mol Biol. 2019;1911:157-168. doi: 10.1007/978-1-4939-8976-8_10.

Abstract

Chronic hepatitis C virus (HCV) infection affects millions of humans throughout the globe, causing liver disease and hepatocellular carcinoma. Persistence of the virus in the infected host can last for decades as a result of a faulty immune response that fails to clear the virus while constituting a major player in viral pathogenesis. In addition to evading immune responses, HCV has evolved intracellular survival strategies that enable persistent replication without directly killing the host cell.After the generation of cell culture infection models for HCV, the knowledge about this virus and host-virus interactions acquired in the last decade has been greatly increased. Interestingly, persistent infection can also be established in cell culture. This model recapitulates persistent HCV RNA replication and viral protein expression as well as infectious progeny virus assembly and secretion and may be used to study not only these aspects of the virus replication cycle but also to study host-virus interactions in a model of prolonged HCV infection. In this chapter, we describe a methodology to generate persistently HCV-infected cultures and to monitor viral load and progeny virus production. Also, we provide generic protocols to study the impact of chemical compounds and host-targeting shRNAs to illustrate the applications of this model in the study of HCV infection in cell culture.

摘要

慢性丙型肝炎病毒(HCV)感染影响着全球数百万人,会引发肝脏疾病和肝细胞癌。由于免疫反应存在缺陷,无法清除病毒,同时在病毒发病机制中起主要作用,病毒在受感染宿主中的持续存在可持续数十年。除了逃避免疫反应外,HCV还进化出细胞内存活策略,使其能够在不直接杀死宿主细胞的情况下进行持续复制。在建立HCV细胞培养感染模型后,过去十年中关于这种病毒以及宿主-病毒相互作用的知识大幅增加。有趣的是,在细胞培养中也能建立持续感染。该模型概括了HCV RNA的持续复制、病毒蛋白表达以及感染性子代病毒的组装和分泌,不仅可用于研究病毒复制周期的这些方面,还可用于在延长的HCV感染模型中研究宿主-病毒相互作用。在本章中,我们描述了一种生成持续感染HCV的培养物并监测病毒载量和子代病毒产生的方法。此外,我们提供了通用方案来研究化合物和靶向宿主的短发夹RNA(shRNA)的影响,以说明该模型在细胞培养中HCV感染研究中的应用。

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