Infection of human hepatocyte chimeric mouse with genetically engineered hepatitis C virus and its susceptibility to interferon

FEBS Lett. 2007 May 15;581(10):1983-7. doi: 10.1016/j.febslet.2007.04.021. Epub 2007 Apr 20.

Abstract

We developed a reverse genetics system of hepatitis C virus (HCV) genotypes 1a and 2a using infectious clones and human hepatocyte chimeric mice. We inoculated cell culture-produced genotype 2a (JFH-1) HCV intravenously. We also injected genotype 1a CV-H77C clone RNA intrahepatically. Mice inoculated with HCV by both procedures developed measurable and transmissible viremia. Interferon (IFN) alpha treatment resulted in greater reduction of genotype 2a HCV levels than genotype 1a, as seen in clinical practice. Genetically engineered HCV infection system should be useful for analysis of the mechanisms of resistance of HCV to IFN and other drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Chimera / virology*
  • Clone Cells
  • Genetic Engineering*
  • Genotype
  • Hepacivirus / drug effects*
  • Hepacivirus / genetics
  • Hepacivirus / physiology
  • Hepatitis C / virology*
  • Hepatocytes / drug effects
  • Hepatocytes / transplantation*
  • Hepatocytes / virology*
  • Humans
  • Interferon-alpha / pharmacology*
  • Mice
  • RNA, Viral / blood
  • Serial Passage
  • Serum Albumin
  • Transcription, Genetic / drug effects
  • Viral Load

Substances

  • Interferon-alpha
  • RNA, Viral
  • Serum Albumin