Glycoprotein M of bovine herpesvirus 1 (BHV-1) is nonessential for replication in cell culture and is involved in inhibition of bovine respiratory syncytial virus F protein induced syncytium formation in recombinant BHV-1 infected cells

Vet Microbiol. 2002 Apr 22;86(1-2):37-49. doi: 10.1016/s0378-1135(01)00489-8.

Abstract

Cell cultures infected with BHV-1/F(syn), a recombinant bovine herpesvirus 1 (BHV-1) which expresses a synthetic open reading frame encoding the fusion (F) protein of the bovine respiratory syncytial virus (BRSV), showed a cytopathic effect (CPE) indistinguishable from that induced by wildtype BHV-1 although transient transfection experiments demonstrated that expression of the F protein leads to formation of large syncytia. Since it has been shown that glycoprotein M (gM) of pseudorabies virus inhibits BRSV F-induced syncytium formation in transient plasmid transfection experiments [Pseudorbies virus glycoprotein M inhibits membrane fusion. J. Virol. 74 (2000) 6760], the gM ORF of wtBHV-1 and BHV-1/F(syn) was interrupted. Infection of cell cultures with the resulting gM(-) mutant of BHV-1/F(syn) led to formation of syncytia, whereas the CPE in gM(-)BHV-1 infected cells was comparable to the CPE in wtBHV-1 infected cultures. Our results demonstrate that gM is not essential for BHV-1 replication in cell culture and that gM is involved in inhibition of the cell fusion activity of the BHV-1 expressed BRSV F protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cattle
  • Cattle Diseases / metabolism
  • Cattle Diseases / virology*
  • Cell Fusion
  • Cells, Cultured
  • DNA, Viral / chemistry
  • Giant Cells / metabolism
  • Giant Cells / virology
  • Herpesviridae Infections / metabolism
  • Herpesviridae Infections / virology*
  • Herpesvirus 1, Bovine / growth & development
  • Herpesvirus 1, Bovine / metabolism*
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Precipitin Tests
  • Recombinant Proteins / metabolism
  • Respiratory Syncytial Viruses / metabolism
  • Sequence Analysis, DNA
  • Transfection
  • Viral Proteins / antagonists & inhibitors*
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*
  • Viral Proteins / physiology
  • Virus Replication / physiology*

Substances

  • DNA, Viral
  • Recombinant Proteins
  • Viral Proteins