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Merck

Cell culture and infection system for hepatitis C virus.

Nature protocols (2007-04-05)
Takanobu Kato, Tomoko Date, Asako Murayama, Kenichi Morikawa, Daisuke Akazawa, Takaji Wakita
RESUMEN

Hepatitis C virus (HCV) infection causes chronic liver disease and is a worldwide health problem. Despite ever-increasing demand for knowledge on viral replication and pathogenesis, detailed analysis has been hampered by a lack of efficient viral culture systems. We isolated HCV genotype 2a strain JFH-1 from a patient with fulminant hepatitis. This strain replicates efficiently in Huh7 cells. Efficient replication and secretion of recombinant viral particles can be obtained in cell culture by transfection of in vitro-transcribed full-length JFH-1 RNA into Huh7 cells. JFH-1 virus generated in cell culture is infectious for both naive Huh7 cells and chimpanzees. The efficiency of viral production and infectivity of generated virus is substantially improved with permissive cell lines. This protocol describes how to use this system, which provides a powerful tool for studying viral life cycle and for the construction of antiviral strategies and the development of effective vaccines. Viral particles can be obtained in 12 days with this protocol.

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Sigma-Aldrich
Seroalbúmina bovina, lyophilized powder, ≥96% (agarose gel electrophoresis)
Sigma-Aldrich
Ácido etilenodiaminotetraacético disodium salt dihydrate, suitable for electrophoresis, for molecular biology, 99.0-101.0% (titration)
Sigma-Aldrich
Cloruro de potasio solution, BioUltra, for molecular biology, ~1 M in H2O