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PMID: 7914548 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Woodchuck hepatitis virus infections: very rapid recovery after a prolonged viremia and infection of virtually every hepatocyte.

Journal of virology ·Vol. 68 ·No. 9 ·1994-09-00 ·Pages 5792-803

Kajino K, Jilbert AR, Saputelli J, Aldrich CE, Cullen J, Mason WS

Abstract

Earlier studies have suggested that transient hepadnavirus infections in mammals are associated with virus replication in a large fraction of hepatocytes. Although the viremia that occurred during transient infections in some individuals would presumably lead to virus replication in all hepatocytes, these studies did not reveal if this was the case. The question of the extent of hepatocyte infection was therefore reinvestigated because of the implications of the results for the mechanisms of virus clearance. Woodchucks were inoculated with woodchuck hepatitis virus, and the course of hepatic infection was determined. These studies indicated that essentially 100% of the hepatocytes became infected in the majority of woodchucks. In 7 of 10 woodchucks, the viral infection was then rapidly cleared from the liver, generally in less than 4 weeks. In another three woodchucks, though productive infection was just as rapidly cleared, viral covalently closed circular DNA remained for weeks to months after other indicators of virus infection had disappeared from the liver. Bromodeoxyuridine labeling and anti-proliferating cell nuclear antigen staining to detect hepatocytes passing through S phase indicated an increase in hepatocyte proliferation during the recovery phase of infection. The rate of cell division appeared to be sufficient to replace no more than 2 to 3% of the hepatocytes per day, at the times at which the biopsies were performed. Histopathologic evaluation of the biopsy samples did not provide evidence for a massive amount of liver regeneration. Models to explain virus clearance, with or without massive immune system-mediated destruction of infected hepatocytes, are reviewed.

MeSH Terms
Animals Antigens, Viral/analysis Cell Division DNA, Viral/metabolism Hepatitis B/microbiology Hepatitis B Virus, Woodchuck/pathogenicity Liver/cytology,microbiology Marmota Nuclear Proteins/metabolism Proliferating Cell Nuclear Antigen Time Factors Viremia Virus Replication
Chemicals
Antigens, Viral DNA, Viral Nuclear Proteins Proliferating Cell Nuclear Antigen
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kajino K
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Jilbert A R
Saputelli J
Aldrich C E
Cullen J
Mason W S
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1994-09-00
Pages
5792-803
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC236983
Subset
IM
Grants
NIAID NIH HHS · AI-18641 · United States
NCI NIH HHS · CA-06927 · United States
NCI NIH HHS · CA-57425 · United States
Analysis Services
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