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J Virol ; 14(1): 20-5, 1974 Jul.
Article in English | MEDLINE | ID: mdl-4365718

ABSTRACT

Replication of herpes simplex virus type 2 (HSV-2) was impeded in KB cells which were blocked in their capacity to synthesize DNA by 2 mM thymidine (TdR). The degree of inhibition was dependent upon the concentration of TdR. In marked contrast, HSV-1 is able to replicate under these conditions. The failure of HSV-2 to replicate is probably due to the inhibition of viral DNA synthesis; there was a marked reduction in the rate of DNA synthesis as well as the total amount of HSV-2 DNA made in the presence of 2 mM TdR. We postulated that the effect of TdR on viral replication occurs at the level of ribonucleotide reductase in a manner similar to KB cells. However, unlike KB cells, an altered ribonucleotide reductase activity, highly resistant to thymidine triphosphate inhibition, was found in extracts of HSV-2-infected KB cells. This activity was present in HSV-2-infected cells incubated in the presence or absence of TdR. Ribonucleotide reductase activity in extracts of HSV-1-infected KB cells showed a similar resistance to thymidine triphosphate inhibition. These results suggest that the effect of TdR on HSV-2 replication occurs at a stage of DNA synthesis other than reduction of cytidine nucleotides to deoxycytidine nucleotides.


Subject(s)
Simplexvirus/drug effects , Thymidine/pharmacology , Virus Replication/drug effects , Amino Acids , Animals , Carcinoma , Cell Division , Cell Line , Cells, Cultured/drug effects , Cells, Cultured/enzymology , Cells, Cultured/metabolism , DNA/biosynthesis , DNA, Viral/biosynthesis , Dose-Response Relationship, Drug , Hypoxanthines , Kidney , Mouth Neoplasms , Protein Biosynthesis , RNA/biosynthesis , Ribonucleotide Reductases/metabolism , Simplexvirus/growth & development , Tritium
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