Expression of Bovine Herpesvirus Type 1 Glycoprotein gI in Transfected Bovine Cells Induces Spontaneous Cell Fusion
- 1 May 1990
- journal article
- research article
- Published by Microbiology Society in Journal of General Virology
- Vol. 71 (5) , 1215-1219
- https://doi.org/10.1099/0022-1317-71-5-1215
Abstract
Bovine MDBK cells were transfected with Rous sarcoma virus-based vectors for constitutive expression of the bovine herpesvirus type 1 (BHV-1) glycoprotein, gI. Cell lines stably expressing recombinant gI were cloned and characterized. Recombinant gI was localized intracellularly, predominantly in a perinuclear region, and on the cell surface. Cells expressing gI exhibited spontaneous polykaryon formation, thus confirming the fusogenic activity described previously in gI-expressing transfected murine LMTK- cells. Teh recombinant form of gI synthesized in transfected MDBK cells was similar in Mr to the form expressed in BHV-1-infected MDBK cells, unlike the recombinant form of gI expressed by LMTK- cells which is deficient in N-linked glycosylation. It was concluded that cell fusion associated with the expression of BHV-1 gI in transfected mammalian cells is a reproducible phenomenon in a number of cell types and is not due to species-specific factors or expression of abnormally glycosylated gI. Cell fusion is a useful in vitro marker for gI function and may contribute to the spread of BHV-1 infections in vivo.This publication has 4 references indexed in Scilit:
- The Effect of Bovine Herpesvirus Type 1 Glycoproteins gI and gIII on Herpesvirus InfectionsJournal of General Virology, 1989
- Expression of bovine herpesvirus 1 glycoproteins gI and gIII in transfected murine cellsJournal of Virology, 1988
- Demonstration of Bovine Viral Diarrhoea Virus in Peripheral Blood Mononuclear Cells of Persistently Infected, Clinically Normal CattleJournal of General Virology, 1987
- Intracellular localization and transport of three different bovine herpesvirus type 1 glycoproteins involved in neutralizationArchiv für die gesamte Virusforschung, 1987