Codon usage, amino acid usage, transfer RNA and amino-acyl-tRNA synthetases in Mimiviruses

Philippe Colson1, Ghislain Fournous, Seydina M Diene

  • 1URMITE UM3, CNRS 7278, IRD 198, INSERM U1905, Institut Hospitalo-Universitaire Méditerranée Infection, Facultés de Médecine et de Pharmacie, Aix-Marseille Université, Marseille, France.

Intervirology
|October 26, 2013
PubMed

Insights

Mimiviruses, giant viruses infecting protists, exhibit unique codon usage distinct from their hosts. Their genetic code and tRNA machinery show adaptations for AT-rich genomes, influencing viral replication.

Area of Science:

  • Virology
  • Genomics
  • Molecular Biology

Background:

  • Mimiviruses are giant viruses with exceptionally large genomes and particle sizes, infecting phagocytic protists like Acanthamoeba.
  • The Mimiviridae family includes diverse lineages, with Mimiviruses being record holders for size.
  • Understanding viral gene expression and host-pathogen interactions is crucial for giant virus research.

Purpose of the Study:

  • To analyze codon and amino acid usage in mimiviruses.
  • To investigate the adaptation of viral transfer RNA (tRNA) and amino acyl-tRNA synthetases to mimivirus genomes.
  • To compare viral and host (Acanthamoeba castellanii) codon usage patterns.

Main Methods:

  • Comparative analysis of codon and amino acid frequencies in mimivirus genomes.
  • Examination of viral tRNA and amino acyl-tRNA synthetase repertoires.
  • Correlation analysis between viral genomic composition and codon usage.

Main Results:

  • Mimivirus codon and amino acid usage significantly differs from Acanthamoeba castellanii, correlating with their high adenine-thymine (AT) genome content.
  • The viral tRNA and amino acyl-tRNA synthetase set is not globally adapted to the virus's codon usage.
  • Specific tRNAs, like Leu(TAA)tRNA, may compensate for the AT-rich codons and aid viral replication.
  • Early expressed viral genes show nucleotide content better adapted to the host's codon usage.

Conclusions:

  • Mimiviruses possess distinct translational machinery and codon usage biases shaped by their AT-rich genomes.
  • Viral tRNAs play a role in accommodating unique codon usage, potentially facilitating replication within Acanthamoeba.
  • Early viral gene expression strategies may involve adaptation to host translational machinery.

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