Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
Hepatology. 2014 Dec;60(6):1838-50. doi: 10.1002/hep.27197. Epub 2014 Jul 14.
Hepatitis C virus (HCV) genotype 3a infection poses a serious health problem worldwide. A significant association has been reported between HCV genotype 3a infections and hepatic steatosis. Nevertheless, virological characterization of genotype 3a HCV is delayed due to the lack of appropriate virus cell culture systems. In the present study, we established the first infectious genotype 3a HCV system by introducing adaptive mutations into the S310 strain. HCV core proteins had different locations in JFH-1 and S310 virus-infected cells. Furthermore, the lipid content in S310 virus-infected cells was higher than Huh7.5.1 cells and JFH-1 virus-infected cells as determined by the lipid droplet staining area.
This genotype 3a infectious cell culture system may be a useful experimental model for studying genotype 3a viral life cycles, molecular mechanisms of pathogenesis, and genotype 3a-specific antiviral drug development.
丙型肝炎病毒(HCV)基因型 3a 感染在全球范围内构成严重的健康问题。据报道,HCV 基因型 3a 感染与肝脂肪变性之间存在显著关联。然而,由于缺乏适当的病毒细胞培养系统,基因型 3a HCV 的病毒学特征描述一直被延迟。在本研究中,我们通过引入适应性突变,在 S310 株中建立了首个感染性基因型 3a HCV 系统。JFH-1 和 S310 病毒感染细胞中的 HCV 核心蛋白具有不同的位置。此外,通过脂滴染色面积测定,S310 病毒感染细胞中的脂质含量高于 Huh7.5.1 细胞和 JFH-1 病毒感染细胞。
该基因型 3a 感染性细胞培养系统可能是研究基因型 3a 病毒生命周期、发病机制的分子机制以及基因型 3a 特异性抗病毒药物开发的有用的实验模型。