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Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
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A ~40-kb flavi-like virus does not encode a known error-correcting mechanism.

Mary E Petrone1,2, Joe Grove3, Julien Mélade1

  • 1Sydney Institute for Infectious Diseases, School of Medical Sciences, The University of Sydney, Sydney, NSW 2006, Australia.

Proceedings of the National Academy of Sciences of the United States of America
|July 17, 2024
PubMed
Summary

A novel ~40 kb flavi-like virus discovered in sponges challenges the RNA virus error threshold. This virus, lacking known exonucleases, suggests alternative strategies for large genome evolution in RNA viruses.

Keywords:
Flaviviridaeerror thresholdevolutionmetatranscriptomicsvirology

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Area of Science:

  • Virology
  • Genomics
  • Evolutionary Biology

Background:

  • A fundamental relationship exists between RNA virus genome size and error rate, known as the error threshold.
  • High mutation rates in RNA viruses typically limit genome size to prevent extinction from deleterious mutations.
  • Exceptions like Nidovirales possess error-correcting exonucleases, enabling larger genomes.

Purpose of the Study:

  • To investigate the evolutionary mechanisms allowing large RNA virus genomes.
  • To explore alternative strategies beyond exonucleases for overcoming the error threshold.
  • To characterize a novel large-genome flavi-like virus found in a sponge.

Main Methods:

  • Metatranscriptomic sequencing to identify novel viruses.
  • Bioinformatic analysis to determine genome size and identify viral proteins.
  • Structural analysis to investigate potential nucleic acid metabolism domains.
  • Phylogenetic inference to determine evolutionary relationships.

Main Results:

  • Discovery of a ~40 kb flavi-like virus in a Haliclona sponge metatranscriptome.
  • The identified virus lacks known viral exonuclease domains.
  • Structural analysis suggests the virus may have acquired cellular nucleic acid metabolism domains.
  • Phylogenetic analysis places the virus as a divergent pesti-like lineage, named 'Maximus pesti-like virus'.

Conclusions:

  • This flavi-like virus achieves a genome size comparable to Nidovirales without relying on known viral exonucleases.
  • RNA viruses have evolved multiple, diverse solutions to overcome the genome size error threshold.
  • The findings expand our understanding of RNA virus genome evolution and adaptation.