Zhong Jin, Gastaminza Pablo, Chung Josan, Stamataki Zania, Isogawa Masanori, Cheng Guofeng, McKeating Jane A, Chisari Francis V
Department of Molecular and Experimental Medicine, SBR-10, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
J Virol. 2006 Nov;80(22):11082-93. doi: 10.1128/JVI.01307-06. Epub 2006 Sep 6.
The virological and cellular consequences of persistent hepatitis C virus (HCV) infection have been elusive due to the absence of the requisite experimental systems. Here, we report the establishment and the characteristics of persistent in vitro infection of human hepatoma-derived cells by a recently described HCV genotype 2a infectious molecular clone. Persistent in vitro infection was characterized by the selection of viral variants that displayed accelerated expansion kinetics, higher peak titers, and increased buoyant densities. Sequencing analysis revealed the selection of a single adaptive mutation in the HCV E2 envelope protein that was largely responsible for the variant phenotype. In parallel, as the virus became more aggressive, cells that were resistant to infection emerged, displaying escape mechanisms operative at the level of viral entry, HCV RNA replication, or both. Collectively, these results reveal the existence of coevolutionary events during persistent HCV infection that favor survival of both virus and host.
由于缺乏必要的实验系统,丙型肝炎病毒(HCV)持续感染的病毒学和细胞后果一直难以捉摸。在此,我们报告了一种最近描述的HCV 2a基因型感染性分子克隆对人肝癌衍生细胞进行持续体外感染的建立过程及特征。持续体外感染的特征是选择了具有加速扩增动力学、更高峰值滴度和增加浮力密度的病毒变体。测序分析揭示了在HCV E2包膜蛋白中选择了一个单一的适应性突变,该突变在很大程度上导致了变体表型。同时,随着病毒变得更具侵袭性,出现了对感染具有抗性的细胞,表现出在病毒进入、HCV RNA复制或两者水平上起作用的逃逸机制。总体而言,这些结果揭示了HCV持续感染期间有利于病毒和宿主生存的共同进化事件的存在。