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PMID: 2293669 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Selective killing of transformed rat cells by minute virus of mice does not require infectious virus production.

Journal of virology ·Vol. 64 ·No. 1 ·1990-01-00 ·Pages 458-62

Guetta E, Mincberg M, Mousset S, Bertinchamps C, Rommelaere J, Tal J

Abstract

Fischer rat fibroblasts, naturally resistant to killing by the fibrotropic strain of minute virus of mice [(parvovirus MVM(p)], became sensitive to MVM when transformed by polyomavirus. This sensitization did not involve an increase in the percentage of cells which synthesized viral capsid antigens or in the percentage of cells which produced infectious virus. The addition of anti-MVM antiserum to the growth medium of MVM-infected cells had only a small effect on their survival rates, indicating that the majority of the killing effect of MVM occurs in a single cycle of infection. The data indicate that cell killing by MVM is independent of infectious virus production and thus support the notion that the preferential cytolytic effect is affected by viral cytotoxic gene products which accumulate to intolerable levels in transformed cells but not in normal ones. Finally, using cells transformed with polyomavirus and genomic and subgenomic clones of polyomavirus, we showed that the extent of sensitization to killing by MVM depended on the transforming agent used.

MeSH Terms
Animals Capsid/analysis Cell Line Cell Survival Cell Transformation, Viral Fibroblasts/cytology Immune Sera Minute Virus of Mice/genetics,growth & development Parvoviridae/genetics Rats Rats, Inbred F344
Chemicals
Immune Sera
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Guetta E
Biology Department, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Mincberg M
Mousset S
Bertinchamps C
Rommelaere J
Tal J
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1990-01-00
Pages
458-62
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC249127
Subset
IM
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