| Literature DB >> 20353362 |
Jens Bukh1, Philip Meuleman, Raymond Tellier, Ronald E Engle, Stephen M Feinstone, Gerald Eder, William C Satterfield, Sugantha Govindarajan, Krzysztof Krawczynski, Roger H Miller, Geert Leroux-Roels, Robert H Purcell.
Abstract
Chimpanzees represent the only animal model for studies of the natural history of hepatitis C virus (HCV). To generate virus stocks of important HCV variants, we infected chimpanzees with HCV strains of genotypes 1-6 and determined the infectivity titer of acute-phase plasma pools in additional animals. The courses of first- and second-passage infections were similar, with early appearance of viremia, HCV RNA titers of >10(4.7) IU/mL, and development of acute hepatitis; the chronicity rate was 56%. The challenge pools had titers of 10(3)-10(5) chimpanzee infectious doses/mL. Human liver-chimeric mice developed high-titer infections after inoculation with the challenge viruses of genotypes 1-6. Inoculation studies with different doses of the genotype 1b pool suggested that a relatively high virus dose is required to consistently infect chimeric mice. The challenge pools represent a unique resource for studies of HCV molecular virology and for studies of pathogenesis, protective immunity, and vaccine efficacy in vivo.Entities:
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Year: 2010 PMID: 20353362 PMCID: PMC2941994 DOI: 10.1086/651579
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226