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A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses

Despite extensive study, little is known about the origins of the mutualistic bacterial endosymbionts that inhabit approximately 10% of the world's insects. In this study, we characterized a novel opportunistic human pathogen, designated “strain HS,” and found that it is a close relative of the...

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Autores principales: Clayton, Adam L., Oakeson, Kelly F., Gutin, Maria, Pontes, Arthur, Dunn, Diane M., von Niederhausern, Andrew C., Weiss, Robert B., Fisher, Mark, Dale, Colin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499248/
https://www.ncbi.nlm.nih.gov/pubmed/23166503
http://dx.doi.org/10.1371/journal.pgen.1002990
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author Clayton, Adam L.
Oakeson, Kelly F.
Gutin, Maria
Pontes, Arthur
Dunn, Diane M.
von Niederhausern, Andrew C.
Weiss, Robert B.
Fisher, Mark
Dale, Colin
author_facet Clayton, Adam L.
Oakeson, Kelly F.
Gutin, Maria
Pontes, Arthur
Dunn, Diane M.
von Niederhausern, Andrew C.
Weiss, Robert B.
Fisher, Mark
Dale, Colin
author_sort Clayton, Adam L.
collection PubMed
description Despite extensive study, little is known about the origins of the mutualistic bacterial endosymbionts that inhabit approximately 10% of the world's insects. In this study, we characterized a novel opportunistic human pathogen, designated “strain HS,” and found that it is a close relative of the insect endosymbiont Sodalis glossinidius. Our results indicate that ancestral relatives of strain HS have served as progenitors for the independent descent of Sodalis-allied endosymbionts found in several insect hosts. Comparative analyses indicate that the gene inventories of the insect endosymbionts were independently derived from a common ancestral template through a combination of irreversible degenerative changes. Our results provide compelling support for the notion that mutualists evolve from pathogenic progenitors. They also elucidate the role of degenerative evolutionary processes in shaping the gene inventories of symbiotic bacteria at a very early stage in these mutualistic associations.
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spelling pubmed-34992482012-11-19 A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses Clayton, Adam L. Oakeson, Kelly F. Gutin, Maria Pontes, Arthur Dunn, Diane M. von Niederhausern, Andrew C. Weiss, Robert B. Fisher, Mark Dale, Colin PLoS Genet Research Article Despite extensive study, little is known about the origins of the mutualistic bacterial endosymbionts that inhabit approximately 10% of the world's insects. In this study, we characterized a novel opportunistic human pathogen, designated “strain HS,” and found that it is a close relative of the insect endosymbiont Sodalis glossinidius. Our results indicate that ancestral relatives of strain HS have served as progenitors for the independent descent of Sodalis-allied endosymbionts found in several insect hosts. Comparative analyses indicate that the gene inventories of the insect endosymbionts were independently derived from a common ancestral template through a combination of irreversible degenerative changes. Our results provide compelling support for the notion that mutualists evolve from pathogenic progenitors. They also elucidate the role of degenerative evolutionary processes in shaping the gene inventories of symbiotic bacteria at a very early stage in these mutualistic associations. Public Library of Science 2012-11-15 /pmc/articles/PMC3499248/ /pubmed/23166503 http://dx.doi.org/10.1371/journal.pgen.1002990 Text en © 2012 Clayton et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Clayton, Adam L.
Oakeson, Kelly F.
Gutin, Maria
Pontes, Arthur
Dunn, Diane M.
von Niederhausern, Andrew C.
Weiss, Robert B.
Fisher, Mark
Dale, Colin
A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses
title A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses
title_full A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses
title_fullStr A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses
title_full_unstemmed A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses
title_short A Novel Human-Infection-Derived Bacterium Provides Insights into the Evolutionary Origins of Mutualistic Insect–Bacterial Symbioses
title_sort novel human-infection-derived bacterium provides insights into the evolutionary origins of mutualistic insect–bacterial symbioses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499248/
https://www.ncbi.nlm.nih.gov/pubmed/23166503
http://dx.doi.org/10.1371/journal.pgen.1002990
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