Hepatitis C Virus NS2 Protein Suppresses RNA Interference in Cells

被引:15
|
作者
Zhou, Hui [1 ]
Qian, Qi [1 ,2 ]
Shu, Ting [2 ,3 ]
Xu, Jiuyue [2 ,4 ]
Kong, Jing [2 ,4 ]
Mu, Jingfang [2 ]
Qiu, Yang [2 ,4 ]
Zhou, Xi [1 ,2 ,4 ]
机构
[1] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Wuhan 430072, Hubei, Peoples R China
[2] Chinese Acad Sci, Ctr Biosafety Megasci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Hubei, Peoples R China
[3] Wuhan Jinyintan Hosp, Ctr Translat Med, Wuhan 430040, Hubei, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatitis C virus (HCV); NS2; Antiviral RNAi; Viral suppressor of RNAi (VSR); IMMUNITY; INHIBITOR; INFLUENZA; ACTS;
D O I
10.1007/s12250-019-00182-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
RNAi interference (RNAi) is an evolutionarily conserved post-transcriptional gene silencing mechanism and has been well recognized as an important antiviral immunity in eukaryotes. Numerous viruses have been shown to encode viral suppressors of RNAi (VSRs) to antagonize antiviral RNAi. Hepatitis C virus (HCV) is a medically important human pathogen that causes acute and chronic hepatitis. In this study, we screened all the nonstructural proteins of HCV and found that HCV NS2 could suppress RNAi induced either by small hairpin RNAs (shRNAs) or small interfering RNAs (siRNAs) in mammalian cells. Moreover, we demonstrated that NS2 could suppress RNAi via its direct interaction with double-stranded RNAs (dsRNAs) and siRNAs, and further identified that the cysteine 184 of NS2 is required for the RNAi suppression activity through a serial of point mutation analyses. Together, our findings uncovered that HCV NS2 can act as a VSR in vitro, thereby providing novel insights into the life cycle and virus-host interactions of HCV.
引用
收藏
页码:436 / 444
页数:9
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