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Evolutionary highways to persistent bacterial infection

Persistent infections require bacteria to evolve from their naïve colonization state by optimizing fitness in the host via simultaneous adaptation of multiple traits, which can obscure evolutionary trends and complicate infection management. Accordingly, here we screen 8 infection-relevant phenotype...

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Autores principales: Bartell, Jennifer A., Sommer, Lea M., Haagensen, Janus A. J., Loch, Anne, Espinosa, Rocio, Molin, Søren, Johansen, Helle Krogh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367392/
https://www.ncbi.nlm.nih.gov/pubmed/30733448
http://dx.doi.org/10.1038/s41467-019-08504-7
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author Bartell, Jennifer A.
Sommer, Lea M.
Haagensen, Janus A. J.
Loch, Anne
Espinosa, Rocio
Molin, Søren
Johansen, Helle Krogh
author_facet Bartell, Jennifer A.
Sommer, Lea M.
Haagensen, Janus A. J.
Loch, Anne
Espinosa, Rocio
Molin, Søren
Johansen, Helle Krogh
author_sort Bartell, Jennifer A.
collection PubMed
description Persistent infections require bacteria to evolve from their naïve colonization state by optimizing fitness in the host via simultaneous adaptation of multiple traits, which can obscure evolutionary trends and complicate infection management. Accordingly, here we screen 8 infection-relevant phenotypes of 443 longitudinal Pseudomonas aeruginosa isolates from 39 young cystic fibrosis patients over 10 years. Using statistical modeling, we map evolutionary trajectories and identify trait correlations accounting for patient-specific influences. By integrating previous genetic analyses of 474 isolates, we provide a window into early adaptation to the host, finding: (1) a 2–3 year timeline of rapid adaptation after colonization, (2) variant “naïve” and “adapted” states reflecting discordance between phenotypic and genetic adaptation, (3) adaptive trajectories leading to persistent infection via three distinct evolutionary modes, and (4) new associations between phenotypes and pathoadaptive mutations. Ultimately, we effectively deconvolute complex trait adaptation, offering a framework for evolutionary studies and precision medicine in clinical microbiology.
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spelling pubmed-63673922019-02-11 Evolutionary highways to persistent bacterial infection Bartell, Jennifer A. Sommer, Lea M. Haagensen, Janus A. J. Loch, Anne Espinosa, Rocio Molin, Søren Johansen, Helle Krogh Nat Commun Article Persistent infections require bacteria to evolve from their naïve colonization state by optimizing fitness in the host via simultaneous adaptation of multiple traits, which can obscure evolutionary trends and complicate infection management. Accordingly, here we screen 8 infection-relevant phenotypes of 443 longitudinal Pseudomonas aeruginosa isolates from 39 young cystic fibrosis patients over 10 years. Using statistical modeling, we map evolutionary trajectories and identify trait correlations accounting for patient-specific influences. By integrating previous genetic analyses of 474 isolates, we provide a window into early adaptation to the host, finding: (1) a 2–3 year timeline of rapid adaptation after colonization, (2) variant “naïve” and “adapted” states reflecting discordance between phenotypic and genetic adaptation, (3) adaptive trajectories leading to persistent infection via three distinct evolutionary modes, and (4) new associations between phenotypes and pathoadaptive mutations. Ultimately, we effectively deconvolute complex trait adaptation, offering a framework for evolutionary studies and precision medicine in clinical microbiology. Nature Publishing Group UK 2019-02-07 /pmc/articles/PMC6367392/ /pubmed/30733448 http://dx.doi.org/10.1038/s41467-019-08504-7 Text en © The Author(s) 2019 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
Bartell, Jennifer A.
Sommer, Lea M.
Haagensen, Janus A. J.
Loch, Anne
Espinosa, Rocio
Molin, Søren
Johansen, Helle Krogh
Evolutionary highways to persistent bacterial infection
title Evolutionary highways to persistent bacterial infection
title_full Evolutionary highways to persistent bacterial infection
title_fullStr Evolutionary highways to persistent bacterial infection
title_full_unstemmed Evolutionary highways to persistent bacterial infection
title_short Evolutionary highways to persistent bacterial infection
title_sort evolutionary highways to persistent bacterial infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367392/
https://www.ncbi.nlm.nih.gov/pubmed/30733448
http://dx.doi.org/10.1038/s41467-019-08504-7
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