A-to-G hypermutation in the genome of lymphocytic choriomeningitis virus

J Virol. 2007 Jan;81(2):457-64. doi: 10.1128/JVI.00067-06. Epub 2006 Oct 4.

Abstract

The interferon-inducible adenosine deaminase that acts on double-stranded RNA (ADAR1-L) has been proposed to be one of the antiviral effector proteins within the complex innate immune response. Here, the potential role of ADAR1-L in the innate immune response to lymphocytic choriomeningitis virus (LCMV), a widely used virus model, was studied. Infection with LCMV clearly upregulated ADAR1-L expression and activity. The editing activity of ADAR1-L on an RNA substrate was not inhibited by LCMV replication. Accordingly, an adenosine-to-guanosine (A-to-G) and uracil-to-cytidine (U-to-C) hypermutation pattern was found in the LCMV genomic RNA in infected cell lines and in mice. In addition, two hypermutated clones with a high level of A-to-G or U-to-C mutations within a short stretch of the viral genome were isolated. Analysis of the functionality of viral glycoprotein revealed that A-to-G- and U-to-C-mutated LCMV genomes coded for nonfunctional glycoprotein at a surprisingly high frequency. Approximately half the GP clones with an amino acid mutation lacked functionality. These results suggest that ADAR1-L-induced mutations in the viral RNA lead to a loss of viral protein function and reduced viral infectivity. This study therefore provides strong support for the contribution of ADAR1-L to the innate antiviral immune response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine
  • Adenosine Deaminase / genetics
  • Adenosine Deaminase / metabolism*
  • Animals
  • Cell Line
  • Genome, Viral*
  • Guanosine
  • Humans
  • Immunity, Innate
  • L Cells
  • Lymphocytic Choriomeningitis / immunology*
  • Lymphocytic Choriomeningitis / virology
  • Lymphocytic choriomeningitis virus / genetics*
  • Lymphocytic choriomeningitis virus / pathogenicity*
  • Mice
  • Mice, Inbred C57BL
  • Mutation*
  • RNA, Double-Stranded / metabolism
  • RNA, Viral / genetics
  • RNA, Viral / metabolism
  • RNA-Binding Proteins
  • Up-Regulation

Substances

  • RNA, Double-Stranded
  • RNA, Viral
  • RNA-Binding Proteins
  • Guanosine
  • ADARB1 protein, human
  • Adenosine Deaminase
  • Adenosine