ORF23 of murine gammaherpesvirus 68 is non-essential for in vitro and in vivo infection

J Gen Virol. 2012 May;93(Pt 5):1076-1080. doi: 10.1099/vir.0.041129-0. Epub 2012 Jan 18.

Abstract

Although ORF23 is conserved among gammaherpesviruses, its role during infection is unknown. Here, we studied the expression of ORF23 of murine gammaherpesvirus 68 (MHV-68) and its role during infection. ORF23 mRNA was detected in infected cells as a late transcript. The ORF23 protein product could be expressed and detected as an N-terminally FLAG-tagged protein by Western blot and indirect immunofluorescence. To investigate the role of ORF23 in the infection cycle of a gammaherpesvirus, we constructed an ORF23 deletion mutant of MHV-68. The analysis of the ORF23 deletion mutant suggested that ORF23 of MHV-68 is neither essential for replication in cell culture nor for lytic or latent infection in vivo. A phenotype of the ORF23 deletion mutant, reflected by a moderate reduction in lytic replication and latency amplification, was only detectable in the face of direct competition to the parental virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Coronaviridae Infections / pathology
  • Coronaviridae Infections / virology
  • Gene Deletion
  • Gene Expression Profiling
  • Lung / virology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Open Reading Frames*
  • Protein Biosynthesis
  • Rhadinovirus / growth & development
  • Rhadinovirus / pathogenicity*
  • Spleen / virology
  • Transcription, Genetic
  • Viral Load
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*
  • Virus Replication*

Substances

  • Viral Proteins