Cell culture-grown hepatitis C virus is infectious in vivo and can be recultured in vitro

被引:340
作者
Lindenbach, BD
Meuleman, P
Ploss, A
Vanwolleghem, T
Syder, AJ
McKeating, JA
Lanford, RE
Feinstone, SM
Major, ME
Leroux-Roels, G
Rice, CM
机构
[1] Rockefeller Univ, Ctr Study Hepatitis C, Lab Virol & Infect Dis, New York, NY 10021 USA
[2] Univ Ghent, Ctr Vaccinol, B-9000 Ghent, Belgium
[3] Ghent Hosp, B-9000 Ghent, Belgium
[4] Univ Birmingham, Sch Med, Biomed Res Inst, Div Immun & Infect, Birmingham B15 2TT, W Midlands, England
[5] SW Natl Primate Res Ctr, Dept Virol & Immunol, San Antonio, TX 78245 USA
[6] SW Fdn Biomed Res, San Antonio, TX 78245 USA
[7] US FDA, Lab Hepatitis Viruses, Div Viral Prod, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA
基金
英国医学研究理事会;
关键词
animal model; pathogenesis; reverse genetics; viral hepatitis;
D O I
10.1073/pnas.0511218103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hepatitis C virus (HCV) is a major cause of chronic liver disease, frequently progressing to cirrhosis and increased risk of hepatocellular carcinoma. Current therapies are inadequate and progress in the field has been hampered by the lack of efficient HCV culture systems. By using a recently described HCV genotype 2a infectious clone that replicates and produces infectious virus in cell culture (HCVcc), we report here that HCVcc strain FL-J6/JFH can establish long-term infections in chimpanzees and in mice containing human liver grafts. Importantly, virus recovered from these animals was highly infectious in cell culture, demonstrating efficient ex vivo culture of HCV. The improved infectivity of animal-derived HCV correlated with virions of a lower average buoyant density than HCVcc, suggesting that physical association with low-density factors influences viral infectivity. These results greatly extend the utility of the HCVcc genetic system to allow the complete in vitro and in vivo dissection of the HCV life cycle.
引用
收藏
页码:3805 / 3809
页数:5
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