Hepatitis E Virus Genome Structure and Replication Strategy

被引:114
|
作者
Kenney, Scott P. [1 ]
Meng, Xiang-Jin [2 ]
机构
[1] Ohio State Univ, Food Anim Hlth Res Program, Wooster, OH 44691 USA
[2] Virginia Polytech Inst & State Univ, Dept Biomed Sci & Pathobiol, Blacksburg, VA 24061 USA
来源
基金
美国国家卫生研究院;
关键词
ENTERS LIVER-CELLS; READING FRAME 1; ORF3; PROTEIN; MUTATIONAL ANALYSIS; NONSTRUCTURAL POLYPROTEIN; HYPERVARIABLE REGION; CULTURED HEPATOMA; CAPSID PROTEIN; CAPPING ENZYME; RHESUS-MONKEYS;
D O I
10.1101/cshperspect.a031724
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hepatitis E virus (HEV) possesses many of the features of other positive-stranded RNA viruses but also adds HEV-specific nuances, making its virus-host interactions unique. Slow virus replication kinetics and fastidious growth conditions, coupled with the historical lack of an efficient cell culture system to propagate the virus, have left many gaps in our understanding of its structure and replication cycle. Recent advances in culturing selected strains of HEV and resolving the 3D structure of the viral capsid are filling in knowledge gaps, but HEV remains an extremely understudied pathogen. Many steps in the HEV life cycle and many aspects of HEV pathogenesis remain unknown, such as the host and viral factors that determine cross-species infection, the HEV-specific receptor(s) on host cells, what determines HEV chronicity and the ability to replicate in extrahepatic sites, and what regulates processing of the open reading frame 1 (ORF1) nonstructural polyprotein.
引用
收藏
页数:17
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