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Unveiling Crucivirus Diversity by Mining Metagenomic Data
mBio
  • Ignacio de la Higuera, Portland State University
  • George Kasun, Portland State University
  • Ellis L. Torrance, Portland State University
  • Alyssa A. Pratt, Portland State University
  • Amberlee Maluenda, Portland State University
  • Jonathan Colombet, Université Clermont Auvergne
  • Maxime Bisseux, Université Clermont Auvergne
  • Viviane Ravet, Université Clermont Auvergne
  • Anisha Dayaram, institut für Neurophysiology, Charité-Universitätsmedizin,
  • Daisy Stainton, University of Arkansas System
  • Simona Kraberger, Arizona State University
  • Peyman Zawar-Reza, University of canterbury
  • Sharyn Goldstien, University of Canterbury
  • James V. Briskie, University of Canterbury
  • Robyn White, University of Canterbury
  • Helen Taylor, University of Otago
  • Christopher Gomez, Kobe University
  • David G. Ainley, HT Harvey and Associates
  • Jon S. Harding, University of Canterbury
  • Rafaela S. Fontenele, Arizona State University
  • Joshua Schreck, Arizona State University
  • Simone Ribeiro, Embrapa Recursos Genéticos e Biotecnologia
  • Stephen A. Oswald, Kobe University
  • Jennifer M. Arnold, Kobe University
  • François Enault, Université Clermont Auvergne
  • Arvind Varsani, Arizona State University
  • Kenneth M. Stedman, Portland State University
Document Type
Article
Publication Date
1-1-2020
Subjects
  • Viruses -- Evolution,
  • Genetic transformation,
  • Genetic recombination,
  • Virology -- Environmental aspects,
  • DNA viruses
Abstract

The discovery of cruciviruses revealed the most explicit example of a common protein homologue between DNA and RNA viruses to date. Cruciviruses are a novel group of circular Rep-encoding single-stranded DNA (ssDNA) (CRESSDNA) viruses that encode capsid proteins that are most closely related to those encoded by RNA viruses in the family Tombusviridae. The apparent chimeric nature of the two core proteins encoded by crucivirus genomes suggests horizontal gene transfer of capsid genes between DNA and RNA viruses. Here, we identified and characterized 451 new crucivirus genomes and 10 capsid-encoding circular genetic elements through de novo assembly and mining of metagenomic data. These genomes are highly diverse, as demonstrated by sequence comparisons and phylogenetic analysis of subsets of the protein sequences they encode. Most of the variation is reflected in the replication-associated protein (Rep) sequences, and much of the sequence diversity appears to be due to recombination. Our results suggest that recombination tends to occur more frequently among groups of cruciviruses with relatively similar capsid proteins and that the exchange of Rep protein domains between cruciviruses is rarer than intergenic recombination. Additionally, we suggest members of the stramenopiles/alveolates/Rhizaria supergroup as possible crucivirus hosts. Altogether, we provide a comprehensive and descriptive characterization of cruciviruses.

Rights

© 2020 de la Higuera et al.


This work is licensed under a Creative Commons Attribution 4.0 International License.

DOI
10.1128/mBio.01410-20
Persistent Identifier
https://archives.pdx.edu/ds/psu/33690
Citation Information
de la Higuera I, Kasun GW, Torrance EL, Pratt AA, Maluenda A, Colombet J, Bisseux M, Ravet V, Dayaram A, Stainton D, Kraberger S, Zawar-Reza P, Goldstien S, Briskie JV, White R, Taylor H, Gomez C, Ainley DG, Harding JS, Fontenele RS, Schreck J, Ribeiro SG, Oswald SA, Arnold JM, Enault F, Varsani A, Stedman KM. 2020. Unveiling crucivirus diversity by mining metagenomic data. mBio 11:e01410-20. https://doi.org/10.1128/mBio.01410-20.