Effect of β-Propiolactone Inactivation of Polyoma Virus on Viral Functions

Author:

Brown A.1,Consigli R. A.1,Zabielski J.1,Weil R.1

Affiliation:

1. Department of Molecular Biology, University of Geneva, Geneva, Switzerland

Abstract

Polyoma virus was inactivated by treatment with β-propiolactone. T-antigen production, polyoma-RNA synthesis, induction of host DNA synthesis (measured by incorporation of labeled thymidine into the cell culture), and in vitro transforming ability were inactivated to a similar degree by various β-propiolactone concentrations (0.25% β-propiolactone reduced these functions approximately 96%), whereas plaque-forming ability and the ability of the virus to replicate its DNA and to synthesize capsid antigen were inactivated by a given concentration of β-propiolactone to a much greater degree (0.25% β-propiolactone led to a reduction of plaque-forming ability of over 8 logs). The significance of these data and their relationship to previously published experiments are discussed.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference20 articles.

1. Radiation target size of the Iytic and transforming ability of polyoma virus;Basilico C.;Proc. Nat. Acad. Sci. U.S.A.,1965

2. Relative target sizes for the inactivation of the transforming and reproductive abilities of polyoma virus;Benjamin T. L.;Proc. Nat. Acad. Sci. U.S.A.,1965

3. Multiplication of polyoma virus. II. Source of constituents for viral deoxyribonucleic acid and protein synthesis;Consigli R. A.;J. Bacteriol.,1966

4. Plaque assay for polyoma virus on primary mouse kidney cell cultures;Consigli R. A.;Appl. Microbiol.,1973

5. Crawford L. 1968. DNA viruses of the Adeno Papilloma and Polyoma group p. 393-434. In H. Fraenkel-Conrat (ed.) Molecular basis of virology. Reinhold New York.

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