Complete replication of hepatitis B virus and hepatitis C virus in a newly developed hepatoma cell line
Author(s) -
Darong Yang,
Chaohui Zuo,
Xiaohong Wang,
Xianghe Meng,
Binbin Xue,
Nianli Liu,
Rong Yu,
Yuwen Qin,
Yimin Gao,
Qiuping Wang,
Jun Hu,
Ling Wang,
Zhou Ze-bin,
Bing Liu,
Deming Tan,
Yang Guan,
Haizhen Zhu
Publication year - 2014
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1320071111
Subject(s) - virology , hbsag , hepatitis b virus , virus , hepatitis c virus , biology , viral replication , cell culture , viral transformation , ns2 3 protease , genetics
The absence of a robust cell culture system for hepatitis B virus (HBV) and hepatitis C virus (HCV) infection has limited the analysis of the virus lifecycle and drug discovery. We have established a hepatoma cell line, HLCZ01, the first cell line, to the authors' knowledge, supporting the entire lifecycle of both HBV and HCV. HBV surface antigen (HBsAg)-positive particles can be observed in the supernatant and the lumen of the endoplasmic reticulum of the cells via electron microscopy. Interestingly, HBV and HCV clinical isolates propagate in HLCZ01 cells. Both viruses replicate in the cells without evidence of overt interference. HBV and HCV entry are blocked by antibodies against HBsAg and human CD81, respectively, and the replication of HBV and HCV is inhibited by antivirals. HLCZ01 cells mount an innate immune response to virus infection. The cell line provides a powerful tool for exploring the mechanisms of virus entry and replication and the interaction between host and virus, facilitating the development of novel antiviral agents and vaccines.
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