Douam Florian, Ploss Alexander
Department of Molecular Biology, Princeton University, Princeton, NJ, USA.
Proteomics. 2015 Jun;15(12):2051-65. doi: 10.1002/pmic.201500009. Epub 2015 May 5.
Hepatitis C virus (HCV) is a major cause of liver disease worldwide. Acute infection often progresses to chronicity resulting frequently in fibrosis, cirrhosis, and in rare cases, in the development of hepatocellular carcinoma. Although HCV has proven to be an arduous object of research and has raised important technical challenges, several experimental models have been developed all over the last two decades in order to improve our understanding of the virus life cycle, pathogenesis and virus-host interactions. The recent development of direct acting-agents, leading to considerable progress in treatment of patients, represents the direct outcomes of these achievements. Proteomic approaches have been of critical help to shed light on several aspect of the HCV biology such as virion composition, viral replication, and virus assembly and to unveil diagnostic or prognostic markers of HCV-induced liver disease. Here, we review how proteomic approaches have led to improve our understanding of HCV life cycle and liver disease, thus highlighting the relevance of these approaches for studying the complex interactions between other challenging human viral pathogens and their host.
丙型肝炎病毒(HCV)是全球肝脏疾病的主要病因。急性感染常进展为慢性感染,频繁导致纤维化、肝硬化,在极少数情况下会发展为肝细胞癌。尽管 HCV 已被证明是一个艰巨的研究对象,并带来了重要的技术挑战,但在过去二十年里,人们开发了多种实验模型,以增进我们对病毒生命周期、发病机制以及病毒与宿主相互作用的理解。直接作用抗病毒药物的最新进展使患者治疗取得了显著成效,这正是这些成果的直接体现。蛋白质组学方法对于阐明 HCV 生物学的多个方面,如病毒体组成、病毒复制和病毒组装,以及揭示 HCV 所致肝病的诊断或预后标志物,起到了至关重要的作用。在此,我们回顾蛋白质组学方法如何增进了我们对 HCV 生命周期和肝病的理解,从而凸显了这些方法对于研究其他具有挑战性的人类病毒病原体与其宿主之间复杂相互作用的相关性。