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ORF23 of murine gammaherpesvirus 68 is non-essential for in vitro and in vivo infection.
Ohno, S; Steer, B; Sattler, C; Adler, H.
Affiliation
  • Ohno S; Institute of Molecular Immunology, Helmholtz Zentrum München - German Research Center for Environmental Health, Munich, Germany.
  • Steer B; Institute of Molecular Immunology, Helmholtz Zentrum München - German Research Center for Environmental Health, Munich, Germany.
  • Sattler C; Institute of Molecular Immunology, Helmholtz Zentrum München - German Research Center for Environmental Health, Munich, Germany.
  • Adler H; Institute of Molecular Immunology, Helmholtz Zentrum München - German Research Center for Environmental Health, Munich, Germany.
J Gen Virol ; 93(Pt 5): 1076-1080, 2012 May.
Article in En | MEDLINE | ID: mdl-22258865
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Proteins / Virus Replication / Open Reading Frames / Rhadinovirus Limits: Animals Language: En Journal: J Gen Virol Year: 2012 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Proteins / Virus Replication / Open Reading Frames / Rhadinovirus Limits: Animals Language: En Journal: J Gen Virol Year: 2012 Document type: Article Affiliation country: Germany