Deletion of the rat cytomegalovirus immediate-early 1 gene results in a virus capable of establishing latency, but with lower levels of acute virus replication and latency that compromise reactivation efficiency

J Gen Virol. 2010 Mar;91(Pt 3):616-21. doi: 10.1099/vir.0.016022-0. Epub 2009 Nov 18.

Abstract

The immediate-early 1 (IE1) and IE2 proteins encoded by the major immediate-early (MIE) transcription unit of cytomegaloviruses are thought to play key roles in the switch between latent- and lytic-cycle infection. Whilst IE2 is essential for triggering the lytic cycle, the exact roles of IE1 have not been resolved. An MIE-exon 4-deleted rat cytomegalovirus (DeltaIE1) failed to synthesize the IE1 protein and did not disperse promyelocytic leukaemia bodies early post-infection, but was still capable of normal replication in fibroblast cell culture. However, DeltaIE1 had a diminished ability to infect salivary glands persistently in vivo and to reactivate from spleen explant cultures ex vivo. Quantification of viral genomes in spleens of infected animals revealed a reduced amount of DeltaIE1 virus produced during acute infection, suggesting a role for IE1 as a regulator in establishing a chronic or persistent infection, rather than in influencing the latency or reactivation processes more directly.

MeSH terms

  • Animals
  • Cells, Cultured
  • DNA, Viral / genetics*
  • Fibroblasts / virology
  • Herpesviridae Infections / virology
  • Immediate-Early Proteins / genetics*
  • In Vitro Techniques
  • Muromegalovirus / genetics
  • Muromegalovirus / physiology*
  • Rats
  • Salivary Glands / virology
  • Sequence Deletion*
  • Spleen / virology
  • Trans-Activators / genetics*
  • Virulence
  • Virus Activation
  • Virus Latency*
  • Virus Replication*

Substances

  • DNA, Viral
  • IE1 protein, cytomegalovirus
  • IE2 protein, Cytomegalovirus
  • Immediate-Early Proteins
  • Trans-Activators