@article{811686ad823c4d4bbd9d03c95acc0a17,
title = "Unveiling crucivirus diversity by mining metagenomic data",
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) (CRESS-DNA) 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 rela-tively 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. IMPORTANCE Viruses are the most abundant biological entities on Earth. In addi-tion to their impact on animal and plant health, viruses have important roles in ecosystem dynamics as well as in the evolution of the biosphere. Circular Rep-encoding single-stranded (CRESS) DNA viruses are ubiquitous in nature, many are agriculturally important, and they appear to have multiple origins from prokaryotic plasmids. A subset of CRESS-DNA viruses, the cruciviruses, have homologues of capsid proteins encoded by RNA viruses. The genetic structure of cruciviruses attests to the transfer of capsid genes between disparate groups of viruses. However, the evolutionary history of cruciviruses is still unclear. By collecting and analyzing cruciviral sequence data, we provide a deeper insight into the evolutionary intricacies of cruciviruses. Our results reveal an unexpected diversity of this virus group, with frequent recombination as an important determinant of variability.",
keywords = "CRESS-DNA viruses, Crucivirus, Environmental virology, Gene transfer, Recombination, Virus evolution",
author = "{de la Higuera}, Ignacio and Kasun, {George W.} and Torrance, {Ellis L.} and Pratt, {Alyssa A.} and Amberlee Maluenda and Jonathan Colombet and Maxime Bisseux and Viviane Ravet and Anisha Dayaram and Daisy Stainton and Simona Kraberger and Peyman Zawar-Reza and Sharyn Goldstien and Briskie, {James V.} and Robyn White and Helen Taylor and Christopher Gomez and Ainley, {David G.} and Harding, {Jon S.} and Fontenele, {Rafaela S.} and Joshua Schreck and Ribeiro, {Simone G.} and Oswald, {Stephen A.} and Arnold, {Jennifer M.} and Fran{\c c}ois Enault and Arvind Varsani and Stedman, {Kenneth M.}",
note = "Funding Information: This work was supported by the NASA Exobiology Program, grant 80NSSC17K0301 (I.D.L.H., G.W.K., E.L.T., A.A.P., and K.M.S.) and the NIH BUILD EXITO Program (A.M.). BUILD EXITO was supported by grants from the National Institutes of Health (UL1GM118964, RL5GM118963, and TL4GM118965) and the Portland State University Ronald E. McNair Scholars Program (E.L.T.), supported by grants from the U.S. Department of Education and Portland State University. The Antarctic field work was supported by the US National Science Foundation (NSF) under grant ANT-0944411, with logistics supplied by the US Antarctic Program. The freshwater work in New Zealand was supported by a grant (UC-E6007) from the American New Zealand Association (USA) awarded to P.Z.-R., C.G., J.S.H., and A.V. The green-lipped mussel work was supported by a grant from the Brian Mason Scientific & Technical Trust of New Zealand awarded to S.G. and A.V. EU-s Horizon 2020 Framework Program for Research and Innovation ({\textquoteleft}Virus-X{\textquoteright}, project no. 685778) supported F.E. Funding Information: This work was supported by the NASA Exobiology Program, grant 80NSSC17K0301 (I.D.L.H., G.W.K., E.L.T., A.A.P., and K.M.S.) and the NIH BUILD EXITO Program (A.M.). BUILD EXITO was supported by grants from the National Institutes of Health (UL1GM118964, RL5GM118963, and TL4GM118965) and the Portland State University Ronald E. McNair Scholars Program (E.L.T.), supported by grants from the U.S. Department of Education and Portland State University. The Antarctic field work was supported by the US National Science Foundation (NSF) under grant ANT-0944411, with logistics supplied by the US Antarctic Program. The freshwater work in New Zealand was supported by a grant (UC-E6007) from the American New Zealand Association (USA) awarded to P.Z.-R., C.G., J.S.H., and A.V. The green-lipped mussel work was supported by a grant from the Brian Mason Scientific & Technical Trust of New Zealand awarded to S.G. and A.V. EU-s Horizon 2020 Framework Program for Research and Innovation (?Virus-X?, project no. 685778) supported F.E. Publisher Copyright: {\textcopyright} 2020 de la Higuera et al.",
year = "2020",
month = sep,
day = "1",
doi = "10.1128/mBio.01410-20",
language = "English (US)",
volume = "11",
pages = "1--17",
journal = "mBio",
issn = "2161-2129",
publisher = "American Society for Microbiology",
number = "5",
}