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Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses

In this study, we aimed at exploring horizontal gene transfer between viruses and Chlorodendraceae green algae (Chlorophyta) using available genomic and transcriptomic sequences for twenty algal strains. We identified a significant number of genes sharing a higher sequence similarity with viral homo...

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Autores principales: Chase, Emily E, Desnues, Christelle, Blanc, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356565/
https://www.ncbi.nlm.nih.gov/pubmed/35949392
http://dx.doi.org/10.1093/ve/veac068
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author Chase, Emily E
Desnues, Christelle
Blanc, Guillaume
author_facet Chase, Emily E
Desnues, Christelle
Blanc, Guillaume
author_sort Chase, Emily E
collection PubMed
description In this study, we aimed at exploring horizontal gene transfer between viruses and Chlorodendraceae green algae (Chlorophyta) using available genomic and transcriptomic sequences for twenty algal strains. We identified a significant number of genes sharing a higher sequence similarity with viral homologues, thus signalling their possible involvement in horizontal gene transfers with viruses. Further characterization showed that many of these genes were clustered in DNA regions of several tens to hundreds of kilobases in size, originally belonging to viruses related to known Tetraselmis spp. viruses (TetV and TsV). In contrast, the remaining candidate HGT genes were randomly dispersed in the algal genomes, were more frequently transcribed, and belonged to large multigene families. The presence of homologues in Viridiplantae suggested that the latter were more likely of algal rather than viral origin. We found a remarkable diversity in polinton-like virus (PLV) elements inserted in Tetraselmis genomes, all of which were most similar to the Tetraselmis striata virus (TsV). The genes of PLV elements are transcriptionally inactive with the notable exception of the homologue of the TVSG_00024 gene of TsV whose function is unknown. We suggest that this gene may be involved in a sentinel process to trigger virus reactivation and excision in response to an environmental stimulus. Altogether, these results provide evidence that TsV-related viruses have a dual lifestyle, alternating between a free viral phase (i.e. virion) and a phase integrated into host genomes.
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spelling pubmed-93565652022-08-09 Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses Chase, Emily E Desnues, Christelle Blanc, Guillaume Virus Evol Research Article In this study, we aimed at exploring horizontal gene transfer between viruses and Chlorodendraceae green algae (Chlorophyta) using available genomic and transcriptomic sequences for twenty algal strains. We identified a significant number of genes sharing a higher sequence similarity with viral homologues, thus signalling their possible involvement in horizontal gene transfers with viruses. Further characterization showed that many of these genes were clustered in DNA regions of several tens to hundreds of kilobases in size, originally belonging to viruses related to known Tetraselmis spp. viruses (TetV and TsV). In contrast, the remaining candidate HGT genes were randomly dispersed in the algal genomes, were more frequently transcribed, and belonged to large multigene families. The presence of homologues in Viridiplantae suggested that the latter were more likely of algal rather than viral origin. We found a remarkable diversity in polinton-like virus (PLV) elements inserted in Tetraselmis genomes, all of which were most similar to the Tetraselmis striata virus (TsV). The genes of PLV elements are transcriptionally inactive with the notable exception of the homologue of the TVSG_00024 gene of TsV whose function is unknown. We suggest that this gene may be involved in a sentinel process to trigger virus reactivation and excision in response to an environmental stimulus. Altogether, these results provide evidence that TsV-related viruses have a dual lifestyle, alternating between a free viral phase (i.e. virion) and a phase integrated into host genomes. Oxford University Press 2022-07-27 /pmc/articles/PMC9356565/ /pubmed/35949392 http://dx.doi.org/10.1093/ve/veac068 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Chase, Emily E
Desnues, Christelle
Blanc, Guillaume
Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses
title Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses
title_full Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses
title_fullStr Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses
title_full_unstemmed Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses
title_short Integrated viral elements suggest the dual lifestyle of Tetraselmis spp. Polinton-like viruses
title_sort integrated viral elements suggest the dual lifestyle of tetraselmis spp. polinton-like viruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356565/
https://www.ncbi.nlm.nih.gov/pubmed/35949392
http://dx.doi.org/10.1093/ve/veac068
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