Yi Minkyung, Lemon Stanley M
Center for Hepatitis Research, Institute for Human Infections and the Department of Microbiology & Immunology, University of Texas Galveston, TX, USA.
Methods Mol Biol. 2009;510:337-46. doi: 10.1007/978-1-59745-394-3_25.
HCV is a small RNA virus belonging to the genus Hepacivirus within the virus family Flaviviridae. Infection with HCV often leads to chronic liver diseases including chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma. Current therapy, based on the use of interferon-alpha (IFN-alpha) in combination with ribavirin, results in limited success, especially in patients infected with the most prevalent genotype 1 viruses. Better therapies are needed, but the inability to propagate HCV in cell culture hampers antiviral drug-discovery efforts. Recently, fully permissive cell-culture systems have been developed that use viral RNA derived from the genotype 2a JFH-1 strain of HCV. Although these systems mark a significant breakthrough for HCV research, the parallel development of a tractable genotype 1a infection system (H77S virus) has provided significant advantages in assessing genotype 1-specific interventions, given the highly heterogeneous nature of HCV. H77S RNA contains five cell culture-adaptive mutations that are placed throughout the nonstructural protein-coding segment of the genome and render the RNA capable of robust replication in human hepatoma (Huh-7) cells. Although significantly less efficient than JFH-1 RNA, H77S RNA produces moderate titers of cell culture-infectious virus when transfected into Huh-7 cells.
丙型肝炎病毒(HCV)是一种小RNA病毒,属于黄病毒科肝炎病毒属。HCV感染常导致慢性肝病,包括慢性肝炎、肝硬化和肝细胞癌。目前基于使用α干扰素(IFN-α)联合利巴韦林的治疗方法成功率有限,尤其是对于感染最常见的1型病毒的患者。需要更好的治疗方法,但由于无法在细胞培养中繁殖HCV,阻碍了抗病毒药物的研发工作。最近,已经开发出了完全允许的细胞培养系统,该系统使用源自HCV 2a JFH-1毒株的病毒RNA。尽管这些系统标志着HCV研究取得了重大突破,但鉴于HCV的高度异质性,可处理的1a基因型感染系统(H77S病毒)的同步开发在评估1型特异性干预措施方面具有显著优势。H77S RNA包含五个细胞培养适应性突变,这些突变分布在基因组的非结构蛋白编码区段,使该RNA能够在人肝癌(Huh-7)细胞中进行强劲复制。尽管效率明显低于JFH-1 RNA,但将H77S RNA转染到Huh-7细胞中时,它会产生中等滴度的细胞培养感染性病毒。