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Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni
Responsible for the majority of bacterial gastroenteritis in the developed world, Campylobacter jejuni is a pervasive pathogen of humans and animals, but its evolution is obscure. In this paper, we exploit contemporary genetic diversity and empirical evidence to piece together the evolutionary histo...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639114/ https://www.ncbi.nlm.nih.gov/pubmed/19008526 http://dx.doi.org/10.1093/molbev/msn264 |
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author | Wilson, Daniel J. Gabriel, Edith Leatherbarrow, Andrew J.H. Cheesbrough, John Gee, Steven Bolton, Eric Fox, Andrew Hart, C. Anthony Diggle, Peter J. Fearnhead, Paul |
author_facet | Wilson, Daniel J. Gabriel, Edith Leatherbarrow, Andrew J.H. Cheesbrough, John Gee, Steven Bolton, Eric Fox, Andrew Hart, C. Anthony Diggle, Peter J. Fearnhead, Paul |
author_sort | Wilson, Daniel J. |
collection | PubMed |
description | Responsible for the majority of bacterial gastroenteritis in the developed world, Campylobacter jejuni is a pervasive pathogen of humans and animals, but its evolution is obscure. In this paper, we exploit contemporary genetic diversity and empirical evidence to piece together the evolutionary history of C. jejuni and quantify its evolutionary potential. Our combined population genetics–phylogenetics approach reveals a surprising picture. Campylobacter jejuni is a rapidly evolving species, subject to intense purifying selection that purges 60% of novel variation, but possessing a massive evolutionary potential. The low mutation rate is offset by a large effective population size so that a mutation at any site can occur somewhere in the population within the space of a week. Recombination has a fundamental role, generating diversity at twice the rate of de novo mutation, and facilitating gene flow between C. jejuni and its sister species Campylobacter coli. We attempt to calibrate the rate of molecular evolution in C. jejuni based solely on within-species variation. The rates we obtain are up to 1,000 times faster than conventional estimates, placing the C. jejuni–C. coli split at the time of the Neolithic revolution. We weigh the plausibility of such recent bacterial evolution against alternative explanations and discuss the evidence required to settle the issue. |
format | Text |
id | pubmed-2639114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26391142009-02-25 Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni Wilson, Daniel J. Gabriel, Edith Leatherbarrow, Andrew J.H. Cheesbrough, John Gee, Steven Bolton, Eric Fox, Andrew Hart, C. Anthony Diggle, Peter J. Fearnhead, Paul Mol Biol Evol Research Articles Responsible for the majority of bacterial gastroenteritis in the developed world, Campylobacter jejuni is a pervasive pathogen of humans and animals, but its evolution is obscure. In this paper, we exploit contemporary genetic diversity and empirical evidence to piece together the evolutionary history of C. jejuni and quantify its evolutionary potential. Our combined population genetics–phylogenetics approach reveals a surprising picture. Campylobacter jejuni is a rapidly evolving species, subject to intense purifying selection that purges 60% of novel variation, but possessing a massive evolutionary potential. The low mutation rate is offset by a large effective population size so that a mutation at any site can occur somewhere in the population within the space of a week. Recombination has a fundamental role, generating diversity at twice the rate of de novo mutation, and facilitating gene flow between C. jejuni and its sister species Campylobacter coli. We attempt to calibrate the rate of molecular evolution in C. jejuni based solely on within-species variation. The rates we obtain are up to 1,000 times faster than conventional estimates, placing the C. jejuni–C. coli split at the time of the Neolithic revolution. We weigh the plausibility of such recent bacterial evolution against alternative explanations and discuss the evidence required to settle the issue. Oxford University Press 2009-02 2008-11-13 /pmc/articles/PMC2639114/ /pubmed/19008526 http://dx.doi.org/10.1093/molbev/msn264 Text en © 2008 The Authors This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wilson, Daniel J. Gabriel, Edith Leatherbarrow, Andrew J.H. Cheesbrough, John Gee, Steven Bolton, Eric Fox, Andrew Hart, C. Anthony Diggle, Peter J. Fearnhead, Paul Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni |
title | Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni |
title_full | Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni |
title_fullStr | Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni |
title_full_unstemmed | Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni |
title_short | Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni |
title_sort | rapid evolution and the importance of recombination to the gastroenteric pathogen campylobacter jejuni |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639114/ https://www.ncbi.nlm.nih.gov/pubmed/19008526 http://dx.doi.org/10.1093/molbev/msn264 |
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