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Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages
The Red Queen hypothesis posits that antagonistic co-evolution between interacting species results in recurrent natural selection via constant cycles of adaptation and counter-adaptation. Interactions such as these are at their most profound in host-parasite systems, with bacteria and their viruses...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653853/ https://www.ncbi.nlm.nih.gov/pubmed/29062062 http://dx.doi.org/10.1038/s41598-017-14285-0 |
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author | Magill, Damian J. Kucher, Phillip A. Krylov, Victor N. Pleteneva, Elena A. Quinn, John P. Kulakov, Leonid A. |
author_facet | Magill, Damian J. Kucher, Phillip A. Krylov, Victor N. Pleteneva, Elena A. Quinn, John P. Kulakov, Leonid A. |
author_sort | Magill, Damian J. |
collection | PubMed |
description | The Red Queen hypothesis posits that antagonistic co-evolution between interacting species results in recurrent natural selection via constant cycles of adaptation and counter-adaptation. Interactions such as these are at their most profound in host-parasite systems, with bacteria and their viruses providing the most intense of battlefields. Studies of bacteriophage evolution thus provide unparalleled insight into the remarkable elasticity of living entities. Here, we report a novel phenomenon underpinning the evolutionary trajectory of a group of dsDNA bacteriophages known as the phiKMVviruses. Employing deep next generation sequencing (NGS) analysis of nucleotide polymorphisms we discovered that this group of viruses generates enhanced intraspecies heterogeneity in their genomes. Our results show the localisation of variants to genes implicated in adsorption processes, as well as variation of the frequency and distribution of SNPs within and between members of the phiKMVviruses. We link error-prone DNA polymerase activity to the generation of variants. Critically, we show trans-activity of this phenomenon (the ability of a phiKMVvirus to dramatically increase genetic variability of a co-infecting phage), highlighting the potential of phages exhibiting such capabilities to influence the evolutionary path of other viruses on a global scale. |
format | Online Article Text |
id | pubmed-5653853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56538532017-11-08 Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages Magill, Damian J. Kucher, Phillip A. Krylov, Victor N. Pleteneva, Elena A. Quinn, John P. Kulakov, Leonid A. Sci Rep Article The Red Queen hypothesis posits that antagonistic co-evolution between interacting species results in recurrent natural selection via constant cycles of adaptation and counter-adaptation. Interactions such as these are at their most profound in host-parasite systems, with bacteria and their viruses providing the most intense of battlefields. Studies of bacteriophage evolution thus provide unparalleled insight into the remarkable elasticity of living entities. Here, we report a novel phenomenon underpinning the evolutionary trajectory of a group of dsDNA bacteriophages known as the phiKMVviruses. Employing deep next generation sequencing (NGS) analysis of nucleotide polymorphisms we discovered that this group of viruses generates enhanced intraspecies heterogeneity in their genomes. Our results show the localisation of variants to genes implicated in adsorption processes, as well as variation of the frequency and distribution of SNPs within and between members of the phiKMVviruses. We link error-prone DNA polymerase activity to the generation of variants. Critically, we show trans-activity of this phenomenon (the ability of a phiKMVvirus to dramatically increase genetic variability of a co-infecting phage), highlighting the potential of phages exhibiting such capabilities to influence the evolutionary path of other viruses on a global scale. Nature Publishing Group UK 2017-10-23 /pmc/articles/PMC5653853/ /pubmed/29062062 http://dx.doi.org/10.1038/s41598-017-14285-0 Text en © The Author(s) 2017 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 Magill, Damian J. Kucher, Phillip A. Krylov, Victor N. Pleteneva, Elena A. Quinn, John P. Kulakov, Leonid A. Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages |
title | Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages |
title_full | Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages |
title_fullStr | Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages |
title_full_unstemmed | Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages |
title_short | Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages |
title_sort | localised genetic heterogeneity provides a novel mode of evolution in dsdna phages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653853/ https://www.ncbi.nlm.nih.gov/pubmed/29062062 http://dx.doi.org/10.1038/s41598-017-14285-0 |
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