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戊型肝炎病毒基因组结构与复制策略。

Hepatitis E Virus Genome Structure and Replication Strategy.

机构信息

Food Animal Health Research Program, The Ohio State University, Wooster, Ohio 44691.

Department of Biomedical Sciences and Pathobiology, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061.

出版信息

Cold Spring Harb Perspect Med. 2019 Jan 2;9(1):a031724. doi: 10.1101/cshperspect.a031724.

Abstract

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.

摘要

戊型肝炎病毒 (HEV) 具有许多正链 RNA 病毒的特征,但也有 HEV 特有的细微差别,使其病毒-宿主相互作用具有独特性。病毒复制动力学缓慢,生长条件苛刻,加上历史上缺乏有效的细胞培养系统来繁殖病毒,这使得我们对其结构和复制周期的了解存在许多空白。最近在培养选定株系的 HEV 和解析病毒衣壳的 3D 结构方面取得的进展填补了知识空白,但 HEV 仍然是一种研究极其不足的病原体。HEV 生命周期的许多步骤和 HEV 发病机制的许多方面仍然未知,例如决定跨物种感染的宿主和病毒因素、宿主细胞上的 HEV 特异性受体、决定 HEV 慢性和在肝外部位复制的能力,以及调节开放阅读框 1 (ORF1) 非结构多蛋白加工的因素。

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