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Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems
Bacteriophage genomes rapidly evolve via mutation and horizontal gene transfer to counter evolving bacterial host defenses; such arms race dynamics should lead to divergence between phages from similar, geographically isolated ecosystems. However, near-identical phage genomes can reoccur over large...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468147/ https://www.ncbi.nlm.nih.gov/pubmed/32879312 http://dx.doi.org/10.1038/s41467-020-18236-8 |
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author | Bellas, Christopher M. Schroeder, Declan C. Edwards, Arwyn Barker, Gary Anesio, Alexandre M. |
author_facet | Bellas, Christopher M. Schroeder, Declan C. Edwards, Arwyn Barker, Gary Anesio, Alexandre M. |
author_sort | Bellas, Christopher M. |
collection | PubMed |
description | Bacteriophage genomes rapidly evolve via mutation and horizontal gene transfer to counter evolving bacterial host defenses; such arms race dynamics should lead to divergence between phages from similar, geographically isolated ecosystems. However, near-identical phage genomes can reoccur over large geographical distances and several years apart, conversely suggesting many are stably maintained. Here, we show that phages with near-identical core genomes in distant, discrete aquatic ecosystems maintain diversity by possession of numerous flexible gene modules, where homologous genes present in the pan-genome interchange to create new phage variants. By repeatedly reconstructing the core and flexible regions of phage genomes from different metagenomes, we show a pool of homologous gene variants co-exist for each module in each location, however, the dominant variant shuffles independently in each module. These results suggest that in a natural community, recombination is the largest contributor to phage diversity, allowing a variety of host recognition receptors and genes to counter bacterial defenses to co-exist for each phage. |
format | Online Article Text |
id | pubmed-7468147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74681472020-09-16 Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems Bellas, Christopher M. Schroeder, Declan C. Edwards, Arwyn Barker, Gary Anesio, Alexandre M. Nat Commun Article Bacteriophage genomes rapidly evolve via mutation and horizontal gene transfer to counter evolving bacterial host defenses; such arms race dynamics should lead to divergence between phages from similar, geographically isolated ecosystems. However, near-identical phage genomes can reoccur over large geographical distances and several years apart, conversely suggesting many are stably maintained. Here, we show that phages with near-identical core genomes in distant, discrete aquatic ecosystems maintain diversity by possession of numerous flexible gene modules, where homologous genes present in the pan-genome interchange to create new phage variants. By repeatedly reconstructing the core and flexible regions of phage genomes from different metagenomes, we show a pool of homologous gene variants co-exist for each module in each location, however, the dominant variant shuffles independently in each module. These results suggest that in a natural community, recombination is the largest contributor to phage diversity, allowing a variety of host recognition receptors and genes to counter bacterial defenses to co-exist for each phage. Nature Publishing Group UK 2020-09-02 /pmc/articles/PMC7468147/ /pubmed/32879312 http://dx.doi.org/10.1038/s41467-020-18236-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bellas, Christopher M. Schroeder, Declan C. Edwards, Arwyn Barker, Gary Anesio, Alexandre M. Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems |
title | Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems |
title_full | Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems |
title_fullStr | Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems |
title_full_unstemmed | Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems |
title_short | Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems |
title_sort | flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468147/ https://www.ncbi.nlm.nih.gov/pubmed/32879312 http://dx.doi.org/10.1038/s41467-020-18236-8 |
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