Kato Takanobu, Date Tomoko, Murayama Asako, Morikawa Kenichi, Akazawa Daisuke, Wakita Takaji
Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Nat Protoc. 2006;1(5):2334-9. doi: 10.1038/nprot.2006.395.
Hepatitis C virus (HCV) infection causes chronic liver disease and is a worldwide health problem. Despite ever-increasing demand for knowledge on viral replication and pathogenesis, detailed analysis has been hampered by a lack of efficient viral culture systems. We isolated HCV genotype 2a strain JFH-1 from a patient with fulminant hepatitis. This strain replicates efficiently in Huh7 cells. Efficient replication and secretion of recombinant viral particles can be obtained in cell culture by transfection of in vitro-transcribed full-length JFH-1 RNA into Huh7 cells. JFH-1 virus generated in cell culture is infectious for both naive Huh7 cells and chimpanzees. The efficiency of viral production and infectivity of generated virus is substantially improved with permissive cell lines. This protocol describes how to use this system, which provides a powerful tool for studying viral life cycle and for the construction of antiviral strategies and the development of effective vaccines. Viral particles can be obtained in 12 days with this protocol.
丙型肝炎病毒(HCV)感染会引发慢性肝病,是一个全球性的健康问题。尽管对病毒复制和发病机制的知识需求不断增加,但由于缺乏有效的病毒培养系统,详细分析受到了阻碍。我们从一名暴发性肝炎患者中分离出了HCV 2a基因型JFH-1毒株。该毒株能在Huh7细胞中高效复制。通过将体外转录的全长JFH-1 RNA转染到Huh7细胞中,可在细胞培养中获得重组病毒颗粒的高效复制和分泌。细胞培养中产生的JFH-1病毒对未感染的Huh7细胞和黑猩猩均具有感染性。使用允许性细胞系可显著提高病毒产生效率和所产生病毒的感染性。本方案描述了如何使用该系统,该系统为研究病毒生命周期、构建抗病毒策略以及开发有效疫苗提供了一个强大的工具。按照本方案,可在12天内获得病毒颗粒。