Biochemical Transformation of Mouse Cells by Varicella-Zoster Virus

Department of Virology, Research Institute for Microbial Diseases, Osaka University, Yamada-kami, Suita, Osaka 565, Japan Mouse L cells lacking the enzyme thymidine kinase (Ltk - ) were infected with varicella-zoster virus (VZV). Even though virus did not replicate in Ltk - cells, the presence of vi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of general virology 1981-10, Vol.56 (2), p.421-430
Hauptverfasser: Yamanishi, Koichi, Matsunaga, Yoshino, Ogino, Takeo, Lopetegui, Patricia
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Department of Virology, Research Institute for Microbial Diseases, Osaka University, Yamada-kami, Suita, Osaka 565, Japan Mouse L cells lacking the enzyme thymidine kinase (Ltk - ) were infected with varicella-zoster virus (VZV). Even though virus did not replicate in Ltk - cells, the presence of virus antigen could be observed by use of an anti-complement immunofluorescent technique at 4 h post-infection and the VZV-specific thymidine kinase could be detected in VZV-infected Ltk - cells. Ltk - cells were converted to a tk + phenotype (Ltk + ) by infection with cell-associated VZV. Clones possessing the ability to grow in selective medium were isolated and cultured successfully for more than 20 passages. One of the clones grew very slowly, but other clones showed almost the same growth rate as that of the parental Ltk - cells. The chromosome analyses of Ltk - cells and transformed cells revealed that the isolated clones were of mouse origin. VZV-specific antigen could be detected in the nuclei of Ltk + cell clones by an immunofluorescent test, while tk activity was greatly enhanced in extracts prepared from transformed cells and its activity was neutralized by hyperimmune serum against VZV. Keywords: varicella-zoster virus, thymidine kinase, biochemical transformation Received 4 February 1981; accepted 27 May 1981.
ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-56-2-421