Hepatitis C - virus host interactions, replication, and viral assembly

被引：40

作者：

Shulla, Ana ^{[1
]}

Randall, Glenn ^{[1
]}

机构：

[1] Univ Chicago, Dept Microbiol, Chicago, IL 60637 USA

来源：

CURRENT OPINION IN VIROLOGY | 2012年 / 2卷 / 06期

关键词：

B TYPE-I; NONSTRUCTURAL PROTEIN 5A; CELL-CULTURE SYSTEMS; 4-KINASE III ALPHA; APOLIPOPROTEIN-E; ISOMERASE ACTIVITY; HUMAN HEPATOCYTES; NS5A PROTEIN; ENTRY; INFECTION;

D O I：

10.1016/j.coviro.2012.09.013

中图分类号：

Q93 [微生物学];

学科分类号：

071005 ; 100705 ;

摘要：

As a relatively simple virus, hepatitis C virus (HCV) depends extensively on its host to infect, replicate and disseminate. HCV has evolved host interactions that result in a restricted tropism, both in terms of cell type and species. Efforts into identifying and validating HCV-host interactions have been hampered by a limited number of infectious virus clones and cell lines that support HCV infection. Despite these limitations, consensus HCV-host interactions have emerged that help define the entry, replication, assembly, and tropism of HCV. This has had important implications in expanding our in vitro and in vivo systems to study HCV replication and pathogenesis. Additionally, a number of these host factors are being targeted for therapeutic development. In this review, we focus on medically relevant pro-viral host factors, their role in HCV biology, and their importance in expanding our model systems.

引用

页码：725 / 732

页数：8

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