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©2007 Baishideng Publishing Group Co.
World J Gastroenterol. May 7, 2007; 13(17): 2442-2445
Published online May 7, 2007. doi: 10.3748/wjg.v13.i17.2442
Published online May 7, 2007. doi: 10.3748/wjg.v13.i17.2442
Figure 1 Infection of different hepatoma cell lines by JFH1 virus.
HepG2 not expressing the CD81 receptor, HepG2 expressing the CD81 receptor and Huh-7 cell- lines were used for the infection. Cells seeded at between 3 and 5. 105 cells per well in 24-well plates were incubated for 2 h at 37°C with 200 mL of culture medium containing infectious JFH1 virus (obtained after successive re-infection of naive Huh-7 cells). Cells were processed and immunostained for the detection of capsid, as previously described (Rouillé et al., 2006, J Virol, 80). The Figure shows the detection of HCV capsid protein in HepG2-CD81 and Huh-7 cells but not in HepG2 cells. Re-infection of naive HepG2-CD81 and Huh-7 cells is effective with the resulting supernatant from each infection.
- Citation: Duverlie G, Wychowski C. Cell culture systems for the hepatitis C virus. World J Gastroenterol 2007; 13(17): 2442-2445
- URL: https://www.wjgnet.com/1007-9327/full/v13/i17/2442.htm
- DOI: https://dx.doi.org/10.3748/wjg.v13.i17.2442