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转互补系统是否适合丙型肝炎病毒生命周期研究?

Are trans-complementation systems suitable for hepatitis C virus life cycle studies?

机构信息

EA4294 Unité de Virologie Clinique et Fondamentale, Université de Picardie Jules Verne, Amiens, France.

出版信息

J Viral Hepat. 2013 Apr;20(4):225-33. doi: 10.1111/jvh.12069. Epub 2013 Feb 14.

DOI:10.1111/jvh.12069
PMID:23490366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7167126/
Abstract

Complementation is a naturally occurring genetic mechanism that has been studied for a number of plus-strand RNA viruses. Although trans-complementation is well documented for Flaviviridae family viruses, the first such system for hepatitis C virus (HCV) was only described in 2005. Since then, the development of a number of HCV trans-complementation models has improved our knowledge of HCV protein functions and interactions, genome replication and viral particle assembly. These models have also been used to produce defective viruses and so improvements are necessary for vaccine assays. This review provides an update on HCV trans-complementation systems, the viral mechanisms studied therewith and the production and characterization of trans-encapsidated particles.

摘要

互补作用是一种自然发生的遗传机制,已经有许多正链 RNA 病毒对此进行了研究。尽管 Flaviviridae 科的病毒的转互补作用已有充分的文献记载,但直到 2005 年才首次描述了丙型肝炎病毒(HCV)的这种系统。此后,许多 HCV 转互补模型的发展提高了我们对 HCV 蛋白功能和相互作用、基因组复制和病毒颗粒组装的认识。这些模型也被用于产生缺陷病毒,因此疫苗检测需要进行改进。本文综述了 HCV 转互补系统、与之相关的病毒机制以及转包裹颗粒的产生和特性。

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2
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J Virol. 2018 Mar 14;92(7). doi: 10.1128/JVI.02182-17. Print 2018 Apr 1.
2
Identification of novel RNA secondary structures within the hepatitis C virus genome reveals a cooperative involvement in genome packaging.丙型肝炎病毒基因组内新型RNA二级结构的鉴定揭示了其在基因组包装中的协同作用。
Sci Rep. 2016 Mar 14;6:22952. doi: 10.1038/srep22952.

本文引用的文献

1
Trans-complemented hepatitis C virus particles as a versatile tool for study of virus assembly and infection.转互补丙型肝炎病毒颗粒作为研究病毒组装和感染的通用工具。
Virology. 2012 Oct 10;432(1):29-38. doi: 10.1016/j.virol.2012.05.033. Epub 2012 Jun 22.
2
Mouse hepatic cells support assembly of infectious hepatitis C virus particles.鼠肝细胞支持传染性丙型肝炎病毒颗粒的组装。
Gastroenterology. 2011 Sep;141(3):1057-66. doi: 10.1053/j.gastro.2011.06.010. Epub 2011 Jun 13.
3
Distinct functions of NS5A in hepatitis C virus RNA replication uncovered by studies with the NS5A inhibitor BMS-790052.通过研究 NS5A 抑制剂 BMS-790052,揭示了 HCV RNA 复制中 NS5A 的不同功能。
J Virol. 2011 Jul;85(14):7312-20. doi: 10.1128/JVI.00253-11. Epub 2011 May 18.
4
Production of hepatitis C virus lacking the envelope-encoding genes for single-cycle infection by providing homologous envelope proteins or vesicular stomatitis virus glycoproteins in trans.通过提供同源包膜蛋白或水疱性口炎病毒糖蛋白在转染中,生产缺乏包膜编码基因的丙型肝炎病毒以实现单周期感染。
J Virol. 2011 Mar;85(5):2138-47. doi: 10.1128/JVI.02313-10. Epub 2010 Dec 15.
5
Production of infectious hepatitis C virus by using RNA polymerase I-mediated transcription.利用 RNA 聚合酶 I 介导的转录生产传染性丙型肝炎病毒。
J Virol. 2010 Jun;84(11):5824-35. doi: 10.1128/JVI.02397-09. Epub 2010 Mar 17.
6
Genetic analysis of the carboxy-terminal region of the hepatitis C virus core protein.丙型肝炎病毒核心蛋白羧基末端区的遗传分析。
J Virol. 2010 Feb;84(4):1666-73. doi: 10.1128/JVI.02043-09. Epub 2009 Dec 9.
7
Vps4 and the ESCRT-III complex are required for the release of infectious hepatitis C virus particles.Vps4 和 ESCRT-III 复合物对于释放感染性丙型肝炎病毒颗粒是必需的。
J Gen Virol. 2010 Feb;91(Pt 2):362-72. doi: 10.1099/vir.0.017285-0. Epub 2009 Oct 14.
8
Characterization of determinants important for hepatitis C virus p7 function in morphogenesis by using trans-complementation.利用反式互补对丙型肝炎病毒p7在形态发生中功能的重要决定因素进行表征。
J Virol. 2009 Nov;83(22):11682-93. doi: 10.1128/JVI.00691-09. Epub 2009 Sep 2.
9
Naturally occurring hepatitis C virus subgenomic deletion mutants replicate efficiently in Huh-7 cells and are trans-packaged in vitro to generate infectious defective particles.天然存在的丙型肝炎病毒亚基因组缺失突变体在Huh-7细胞中能高效复制,并在体外进行转包装以产生感染性缺陷颗粒。
J Virol. 2009 Sep;83(18):9079-93. doi: 10.1128/JVI.00308-09. Epub 2009 Jul 8.
10
Trans-complementation of an NS2 defect in a late step in hepatitis C virus (HCV) particle assembly and maturation.丙型肝炎病毒(HCV)颗粒组装和成熟后期NS2缺陷的反式互补。
PLoS Pathog. 2009 May;5(5):e1000403. doi: 10.1371/journal.ppat.1000403. Epub 2009 May 1.