Shi Guoli, Suzuki Tetsuro
Antiviral Immunity and Resistance Section, HIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institute, Frederick, MD, United States.
Department of Virology and Parasitology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Front Microbiol. 2018 Mar 7;9:396. doi: 10.3389/fmicb.2018.00396. eCollection 2018.
Hepatitis C virus (HCV), a major etiologic agent of human liver diseases, is a positive-sense single-stranded RNA virus and is classified in the family. Although research findings for the assembly of HCV particles are accumulating due to development of HCV cell culture system, the mechanism(s) by which the HCV genome becomes encapsidated remains largely unclear. In general, viral RNA represents only a small fraction of the RNA molecules in the cells infected with RNA viruses, but the viral genomic RNA is considered to selectively packaged into virions. It was recently demonstrated that HCV RNAs containing 3' end of the genome are selectively incorporated into virus particles during the assembly process and the 3' untranslated region functions as a -acting element for RNA packaging. Here, we discuss the molecular basis of RNA encapsidation of HCV and classical flaviviruses, contrast with the packaging mechanism of HIV-1.
丙型肝炎病毒(HCV)是人类肝脏疾病的主要病原体,是一种正义单链RNA病毒,属于该科。尽管由于HCV细胞培养系统的发展,关于HCV颗粒组装的研究结果不断积累,但HCV基因组被衣壳化的机制在很大程度上仍不清楚。一般来说,病毒RNA在感染RNA病毒的细胞中仅占RNA分子的一小部分,但病毒基因组RNA被认为是选择性地包装到病毒粒子中。最近有研究表明,含有基因组3'端的HCV RNA在组装过程中被选择性地整合到病毒颗粒中,并且3'非翻译区作为RNA包装的顺式作用元件发挥作用。在此,我们讨论HCV和经典黄病毒RNA衣壳化的分子基础,并与HIV-1的包装机制进行对比。