Novel Cell Culture-Adapted Genotype 2a Hepatitis C Virus Infectious Clone

被引:38
作者
Date, Tomoko [1 ]
Kato, Takanobu [1 ]
Kato, Junko [2 ,3 ]
Takahashi, Hitoshi [1 ]
Morikawa, Kenichi [1 ]
Akazawa, Daisuke [1 ,4 ]
Murayama, Asako [1 ]
Tanaka-Kaneko, Keiko [5 ]
Sata, Tetsutaro [5 ]
Tanaka, Yasuhito [6 ]
Mizokami, Masashi [7 ]
Wakita, Takaji [1 ]
机构
[1] Natl Inst Infect Dis, Dept Virol 2, Tokyo, Japan
[2] Tokyo Womens Med Univ, Inst Geriatr, Tokyo, Japan
[3] Showa Univ, Sch Med, Dept Med, Div Gastroenterol, Tokyo 142, Japan
[4] Toray Industries Ltd, Pharmaceut Res Labs, Kanagawa, Japan
[5] Natl Inst Infect Dis, Dept Pathol, Tokyo, Japan
[6] Nagoya City Univ, Dept Virol & Liver Unit, Grad Sch Med Sci, Nagoya, Aichi, Japan
[7] Natl Ctr Global Hlth & Med, Res Ctr Hepatitis & Immunol, Chiba, Japan
基金
日本学术振兴会;
关键词
AMINO-ACID SUBSTITUTIONS; NON-A; EFFICIENT REPLICATION; JFH-1; STRAIN; CDNA-CLONE; INTERFERON; RIBAVIRIN; SENSITIVITY; MUTATIONS; LIVER;
D O I
10.1128/JVI.07235-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Although the recently developed infectious hepatitis C virus system that uses the JFH-1 clone enables the study of whole HCV viral life cycles, limited particular HCV strains have been available with the system. In this study, we isolated another genotype 2a HCV cDNA, the JFH-2 strain, from a patient with fulminant hepatitis. JFH-2 subgenomic replicons were constructed. HuH-7 cells transfected with in vitro transcribed replicon RNAs were cultured with G418, and selected colonies were isolated and expanded. From sequencing analysis of the replicon genome, several mutations were found. Some of the mutations enhanced JFH-2 replication; the 2217AS mutation in the NS5A interferon sensitivity-determining region exhibited the strongest adaptive effect. Interestingly, a full-length chimeric or wild-type JFH-2 genome with the adaptive mutation could replicate in Huh-7.5.1 cells and produce infectious virus after extensive passages of the virus genome-replicating cells. Virus infection efficiency was sufficient for autonomous virus propagation in cultured cells. Additional mutations were identified in the infectious virus genome. Interestingly, full-length viral RNA synthesized from the cDNA clone with these adaptive mutations was infectious for cultured cells. This approach may be applicable for the establishment of new infectious HCV clones.
引用
收藏
页码:10805 / 10820
页数:16
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