Ando Tomomi, Aizaki Hideki, Sugiyama Masaya, Date Tomoko, Hayashi Kazuhiko, Ishigami Masatoshi, Katano Yoshiaki, Goto Hidemi, Mizokami Masashi, Muramatsu Masamichi, Kuroda Makoto, Wakita Takaji
Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
Department of Viral Pathogenesis and Controls, National Center for Global Health and Medicine, Chiba, Japan.
Biochem Biophys Rep. 2022 Aug 29;32:101327. doi: 10.1016/j.bbrep.2022.101327. eCollection 2022 Dec.
The viral genome quasispecies composition of hepatitis C virus (HCV) could have important implications to viral pathogenesis and resistance to anti-viral treatment. The purpose of the present study was to profile the HCV RNA quasispecies. We developed a strategy to determine the full-length HCV genome sequences co-existing within a single patient serum by using next-generation sequencing technologies. The isolated viral clones were divided into the groups that can be distinguished by core amino acid 70 substitution. Subsequently, we determined HCV full-length genome sequences of three independent dominant species co-existing in the sequential serum with a 7-year interval. From phylogenetic analysis, these dominant species evolved independently. Our study demonstrated that multiple dominant species co-existed in patient sera and evolved independently.
丙型肝炎病毒(HCV)的病毒基因组准种组成可能对病毒发病机制及抗病毒治疗耐药性具有重要影响。本研究的目的是分析HCV RNA准种。我们开发了一种策略,通过使用新一代测序技术来确定存在于单个患者血清中的全长HCV基因组序列。分离出的病毒克隆被分为可通过核心氨基酸70替换加以区分的组。随后,我们确定了在间隔7年的连续血清中共同存在的三个独立优势种的HCV全长基因组序列。通过系统发育分析,这些优势种是独立进化的。我们的研究表明,多个优势种共存于患者血清中并独立进化。