Severe acute respiratory syndrome coronavirus protein 6 is required for optimal replication

J Virol. 2009 Mar;83(5):2368-73. doi: 10.1128/JVI.02371-08. Epub 2008 Dec 17.

Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV) encodes several accessory proteins of unknown function. One of these proteins, protein 6 (p6), which is encoded by ORF6, enhances virus replication when introduced into a heterologous murine coronavirus (mouse hepatitis virus [MHV]) but is not essential for optimal SARS-CoV replication after infection at a relatively high multiplicity of infection (MOI). Here, we reconcile these apparently conflicting results by showing that p6 enhances SARS-CoV replication to nearly the same extent as when expressed in the context of MHV if cells are infected at a low MOI and accelerates disease in mice transgenic for the human SARS-CoV receptor.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Interferon-gamma / pharmacology
  • Mice
  • Mice, Transgenic
  • Open Reading Frames
  • Receptors, Virus / metabolism
  • STAT1 Transcription Factor / metabolism
  • Severe Acute Respiratory Syndrome / virology
  • Severe acute respiratory syndrome-related coronavirus / metabolism*
  • Severe acute respiratory syndrome-related coronavirus / pathogenicity
  • Severe acute respiratory syndrome-related coronavirus / physiology
  • Viral Proteins / metabolism*
  • Virus Replication*

Substances

  • Receptors, Virus
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Viral Proteins
  • protein 6, SARS virus
  • Interferon-gamma