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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6367392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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