Longitudinal Analysis of Hepatitis C Virus Infection and Genetic Drift of the Hypervariable Region

Hepatitis C virus (HCV) infections in a cohort of chimpanzees were studied retrospectively. All animals had been inoculated intravenously with materials derived from a single-source chimpanzee plasma implicated in non-A, non-B hepatitis, prepared by extensive ultracentrifugation. Anti-HCV and HCV RN...

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Published inThe Journal of infectious diseases Vol. 169; no. 6; pp. 1226 - 1235
Main Authors van Doorn, Leen-Jan, Quint, Wim, Tsiquaye, Kwesi, Voermans, Jolanda, Paelinck, Dimitri, Kos, Ton, Maertens, Geert, Schellekens, Huub, Murray, Kenneth
Format Journal Article
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.06.1994
University of Chicago Press
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Summary:Hepatitis C virus (HCV) infections in a cohort of chimpanzees were studied retrospectively. All animals had been inoculated intravenously with materials derived from a single-source chimpanzee plasma implicated in non-A, non-B hepatitis, prepared by extensive ultracentrifugation. Anti-HCV and HCV RNA were monitored by the confirmatory line immunoassay and by an RNA-capture polymerase chain reaction method, respectively. In a chronically infected chimpanzee, HCV RNA was detectable after 32 days and throughout the acute phase, dropped transiently below detection level, and became detectable again. In 3 other chimpanzees with acute resolving infections, HCV RNA was detected 7–11 days after inoculation and became permanently undetectable after alanine aminotransferase normalization. Various anti-HCV profiles were detected among the chimpanzees. Analysis of the hypervariable region in E2/NS1 in 7 chimpanzees suggested genome stability on transmission, revealed different mutation frequencies during chronic infection, and suggested the importance of immune selection during chronic HCV infection.
Bibliography:Reprints or correspondence: Dr. L.-J. van Doorn, Diagnostic Center SSDZ, Dept. of Molecular Biology, P.O. Box 5010, 2600 GA Delft, Netherlands.
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ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/169.6.1226