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Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium

This study describes novel single-stranded DNA phages isolated from common bean agriculture soils by infection of the nitrogen-fixing symbiotic bacteria Rhizobium etli and R. phaseoli. A total of 29 phages analyzed have 4.3–6 kb genomes in size and GC 59–60%. They belong to different clades unrelate...

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Autores principales: Van Cauwenberghe, Jannick, Santamaría, Rosa I., Bustos, Patricia, González, Víctor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512667/
https://www.ncbi.nlm.nih.gov/pubmed/36177468
http://dx.doi.org/10.3389/fmicb.2022.990394
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author Van Cauwenberghe, Jannick
Santamaría, Rosa I.
Bustos, Patricia
González, Víctor
author_facet Van Cauwenberghe, Jannick
Santamaría, Rosa I.
Bustos, Patricia
González, Víctor
author_sort Van Cauwenberghe, Jannick
collection PubMed
description This study describes novel single-stranded DNA phages isolated from common bean agriculture soils by infection of the nitrogen-fixing symbiotic bacteria Rhizobium etli and R. phaseoli. A total of 29 phages analyzed have 4.3–6 kb genomes in size and GC 59–60%. They belong to different clades unrelated to other Microviridae subfamilies. Three-dimensional models of the major capsid protein (MCP) showed a conserved β-barrel structural “jelly-roll” fold. A variable-length loop in the MCPs distinguished three Rhizobium microvirus groups. Microviridae subfamilies were consistent with viral clusters determined by the protein-sharing network. All viral clusters, except for Bullavirinae, included mostly microviruses identified in metagenomes from distinct ecosystems. Two Rhizobium microvirus clusters, chaparroviruses, and chicoviruses, were included within large viral unknown clusters with microvirus genomes identified in diverse metagenomes. A third Rhizobium microvirus cluster belonged to the subfamily Amoyvirinae. Phylogenetic analysis of the MCP confirms the divergence of the Rhizobium microviruses into separate clades. The phylogeny of the bacterial hosts matches the microvirus MCP phylogeny, suggesting a coevolutionary history between the phages and their bacterial host. This study provided essential biological information on cultivated microvirus for understanding the evolution and ecological diversification of the Microviridae family in diverse microbial ecosystems.
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spelling pubmed-95126672022-09-28 Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium Van Cauwenberghe, Jannick Santamaría, Rosa I. Bustos, Patricia González, Víctor Front Microbiol Microbiology This study describes novel single-stranded DNA phages isolated from common bean agriculture soils by infection of the nitrogen-fixing symbiotic bacteria Rhizobium etli and R. phaseoli. A total of 29 phages analyzed have 4.3–6 kb genomes in size and GC 59–60%. They belong to different clades unrelated to other Microviridae subfamilies. Three-dimensional models of the major capsid protein (MCP) showed a conserved β-barrel structural “jelly-roll” fold. A variable-length loop in the MCPs distinguished three Rhizobium microvirus groups. Microviridae subfamilies were consistent with viral clusters determined by the protein-sharing network. All viral clusters, except for Bullavirinae, included mostly microviruses identified in metagenomes from distinct ecosystems. Two Rhizobium microvirus clusters, chaparroviruses, and chicoviruses, were included within large viral unknown clusters with microvirus genomes identified in diverse metagenomes. A third Rhizobium microvirus cluster belonged to the subfamily Amoyvirinae. Phylogenetic analysis of the MCP confirms the divergence of the Rhizobium microviruses into separate clades. The phylogeny of the bacterial hosts matches the microvirus MCP phylogeny, suggesting a coevolutionary history between the phages and their bacterial host. This study provided essential biological information on cultivated microvirus for understanding the evolution and ecological diversification of the Microviridae family in diverse microbial ecosystems. Frontiers Media S.A. 2022-09-13 /pmc/articles/PMC9512667/ /pubmed/36177468 http://dx.doi.org/10.3389/fmicb.2022.990394 Text en Copyright © 2022 Van Cauwenberghe, Santamaría, Bustos and González. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Van Cauwenberghe, Jannick
Santamaría, Rosa I.
Bustos, Patricia
González, Víctor
Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium
title Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium
title_full Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium
title_fullStr Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium
title_full_unstemmed Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium
title_short Novel lineages of single-stranded DNA phages that coevolved with the symbiotic bacteria Rhizobium
title_sort novel lineages of single-stranded dna phages that coevolved with the symbiotic bacteria rhizobium
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512667/
https://www.ncbi.nlm.nih.gov/pubmed/36177468
http://dx.doi.org/10.3389/fmicb.2022.990394
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