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 in | The Journal of infectious diseases Vol. 169; no. 6; pp. 1226 - 1235 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
01.06.1994
University of Chicago Press |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | Reprints or correspondence: Dr. L.-J. van Doorn, Diagnostic Center SSDZ, Dept. of Molecular Biology, P.O. Box 5010, 2600 GA Delft, Netherlands. ark:/67375/HXZ-5GN318TN-1 istex:507176D70A841E6832EDB0DB0156BE191FC654C1 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1093/infdis/169.6.1226 |