Different rates of (non-)synonymous mutations in astrovirus genes; correlation with gene function

Virol J. 2007 Mar 7:4:25. doi: 10.1186/1743-422X-4-25.

Abstract

Background: Complete genome sequences of the Astroviridae include human, non-human mammalian and avian species. A consensus topology of astroviruses has been derived from nucleotide substitutions in the full-length genomes and from non-synonymous nucleotide substitutions in each of the three ORFs. Analyses of synonymous substitutions displayed a loss of tree structure, suggesting either saturation of the substitution model or a deviant pattern of synonymous substitutions in certain virus species.

Results: We analyzed the complete Astroviridae family for the inference of adaptive molecular evolution at sites and in branches. High rates of synonymous mutations are observed among the non-human virus species. Deviant patterns of synonymous substitutions are found in the capsid structural genes. Purifying selection is a dominant force among all astrovirus genes and only few codon sites showed values for the dN/dS ratio that may indicate site-specific molecular adaptation during virus evolution. One of these sites is the glycine residue of a RGD motif in ORF2 of human astrovirus serotype 1. RGD or similar integrin recognition motifs are present in nearly all astrovirus species.

Conclusion: Phylogenetic analysis directed by maximum likelihood approximation allows the inclusion of significantly more evolutionary history and thereby, improves the estimation of dN and dS. Sites with enhanced values for dN/dS are prominent at domains in charge of environmental communication (f.i. VP27 and domain 4 in ORF1a) more than at domains dedicated to intrinsic virus functions (f.i. VP34 and ORF1b (the virus polymerase)). Integrin recognition may play a key role in astrovirus to target cell attachment.

MeSH terms

  • Animals
  • Astroviridae / classification
  • Astroviridae / genetics*
  • Astroviridae / metabolism
  • Birds
  • Capsid Proteins / genetics
  • Capsid Proteins / metabolism*
  • Cats
  • Evolution, Molecular
  • Genes, Viral*
  • Humans
  • Mutation*
  • Open Reading Frames / genetics
  • Selection, Genetic
  • Sheep
  • Species Specificity
  • Swine
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*

Substances

  • Capsid Proteins
  • Viral Proteins