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Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations

How and at what pace bacteria evolve when colonizing healthy hosts remains unclear. Here, by monitoring evolution for more than six thousand generations in the mouse gut, we show that the successful colonization of an invader Escherichia coli depends on the diversity of the existing microbiota and t...

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Autores principales: Frazão, N., Konrad, A., Amicone, M., Seixas, E., Güleresi, D., Lässig, M., Gordo, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509342/
https://www.ncbi.nlm.nih.gov/pubmed/36153389
http://dx.doi.org/10.1038/s41467-022-33412-8
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author Frazão, N.
Konrad, A.
Amicone, M.
Seixas, E.
Güleresi, D.
Lässig, M.
Gordo, I.
author_facet Frazão, N.
Konrad, A.
Amicone, M.
Seixas, E.
Güleresi, D.
Lässig, M.
Gordo, I.
author_sort Frazão, N.
collection PubMed
description How and at what pace bacteria evolve when colonizing healthy hosts remains unclear. Here, by monitoring evolution for more than six thousand generations in the mouse gut, we show that the successful colonization of an invader Escherichia coli depends on the diversity of the existing microbiota and the presence of a closely related strain. Following colonization, two modes of evolution were observed: one in which diversifying selection leads to long-term coexistence of ecotypes and a second in which directional selection propels selective sweeps. These modes can be quantitatively distinguished by the statistics of mutation trajectories. In our experiments, diversifying selection was marked by the emergence of metabolic mutations, and directional selection by acquisition of prophages, which bring their own benefits and costs. In both modes, we observed parallel evolution, with mutation accumulation rates comparable to those typically observed in vitro on similar time scales. Our results show how rapid ecotype formation and phage domestication can be in the mammalian gut.
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spelling pubmed-95093422022-09-26 Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations Frazão, N. Konrad, A. Amicone, M. Seixas, E. Güleresi, D. Lässig, M. Gordo, I. Nat Commun Article How and at what pace bacteria evolve when colonizing healthy hosts remains unclear. Here, by monitoring evolution for more than six thousand generations in the mouse gut, we show that the successful colonization of an invader Escherichia coli depends on the diversity of the existing microbiota and the presence of a closely related strain. Following colonization, two modes of evolution were observed: one in which diversifying selection leads to long-term coexistence of ecotypes and a second in which directional selection propels selective sweeps. These modes can be quantitatively distinguished by the statistics of mutation trajectories. In our experiments, diversifying selection was marked by the emergence of metabolic mutations, and directional selection by acquisition of prophages, which bring their own benefits and costs. In both modes, we observed parallel evolution, with mutation accumulation rates comparable to those typically observed in vitro on similar time scales. Our results show how rapid ecotype formation and phage domestication can be in the mammalian gut. Nature Publishing Group UK 2022-09-24 /pmc/articles/PMC9509342/ /pubmed/36153389 http://dx.doi.org/10.1038/s41467-022-33412-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Frazão, N.
Konrad, A.
Amicone, M.
Seixas, E.
Güleresi, D.
Lässig, M.
Gordo, I.
Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations
title Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations
title_full Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations
title_fullStr Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations
title_full_unstemmed Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations
title_short Two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations
title_sort two modes of evolution shape bacterial strain diversity in the mammalian gut for thousands of generations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509342/
https://www.ncbi.nlm.nih.gov/pubmed/36153389
http://dx.doi.org/10.1038/s41467-022-33412-8
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