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PMID: 211260 Published · ppublish English Journal Article

Interference with simian virus 40 DNA replication by adenovirus type 2 during mixed infection of monkey cells.

Journal of virology ·Vol. 27 ·No. 2 ·1978-08-00 ·Pages 275-87

van Roy F, Fiers W

Abstract

Infection of monkey cells with human adenovirus (Ad) is abortive, but the infection can be enhanced by coinfecting with simian virus 40 (SV40). However, in the coinfected monkey cells, Ad interferes strongly with SV40 DNA biosynthesis. This interference was found to be a reproducible, delicately controlled phenomenon that was proportional to the multiplicity of infection of Ad and dependent on the active expression of the Ad genome. Newly synthesized SV40 DNA was not broken down in cells after delayed superinfection with Ad, and several early events of SV40 infection such as adsorption, penetration, uncoating, induction of cellular DNA synthesis, and enhancement of Ad infection were not markedly influenced by Ad-mediated interference. It is unlikely that interference is simply due to competition between SV40 and Ad for metabolites, enzymes, or replication sites. The interference effect could be partially neutralized by an increase in the multiplicity of coinfecting SV40 or by an increase in the time interval between SV40 infection and Ad coinfection. Interference was shown to be due to the activity of an Ad early gene product. However, the detailed mechanism of this Ad interference is still unclear.

MeSH Terms
Adenoviruses, Human/growth & development Animals Cell Line DNA/biosynthesis DNA Replication DNA, Viral/biosynthesis Haplorhini Simian virus 40/growth & development,metabolism Viral Interference Virus Replication
Chemicals
DNA, Viral DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
van Roy F
Fiers W
References (27)
27 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1978-08-00
Pages
275-87
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC354165
Subset
IM
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