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Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation
In cystic fibrosis (CF) patients, chronic airway infection by Pseudomonas leads to progressive lung destruction ultimately requiring lung transplantation (LT). Following LT, CF-adapted Pseudomonas strains, potentially originating from the sinuses, may seed the allograft leading to infections and red...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240337/ https://www.ncbi.nlm.nih.gov/pubmed/28094327 http://dx.doi.org/10.1038/srep40309 |
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author | Beaume, M. Köhler, T. Greub, G. Manuel, O. Aubert, J-D. Baerlocher, L. Farinelli, L. Buckling, A. van Delden, C. |
author_facet | Beaume, M. Köhler, T. Greub, G. Manuel, O. Aubert, J-D. Baerlocher, L. Farinelli, L. Buckling, A. van Delden, C. |
author_sort | Beaume, M. |
collection | PubMed |
description | In cystic fibrosis (CF) patients, chronic airway infection by Pseudomonas leads to progressive lung destruction ultimately requiring lung transplantation (LT). Following LT, CF-adapted Pseudomonas strains, potentially originating from the sinuses, may seed the allograft leading to infections and reduced allograft survival. We investigated whether CF-adapted Pseudomonas populations invade the donor microbiota and adapt to the non-CF allograft. We collected sequential Pseudomonas isolates and airway samples from a CF-lung transplant recipient during two years, and followed the dynamics of the microbiota and Pseudomonas populations. We show that Pseudomonas invaded the host microbiota within three days post-LT, in association with a reduction in richness and diversity. A dominant mucoid and hypermutator mutL lineage was replaced after 11 days by non-mucoid strains. Despite antibiotic therapy, Pseudomonas dominated the allograft microbiota until day 95. We observed positive selection of pre-LT variants and the appearance of novel mutations. Phenotypic adaptation resulted in increased biofilm formation and swimming motility capacities. Pseudomonas was replaced after 95 days by a microbiota dominated by Actinobacillus. In conclusion, mucoid Pseudomonas adapted to the CF-lung remained able to invade the allograft. Selection of both pre-existing non-mucoid subpopulations and of novel phenotypic traits suggests rapid adaptation of Pseudomonas to the non-CF allograft. |
format | Online Article Text |
id | pubmed-5240337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52403372017-01-23 Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation Beaume, M. Köhler, T. Greub, G. Manuel, O. Aubert, J-D. Baerlocher, L. Farinelli, L. Buckling, A. van Delden, C. Sci Rep Article In cystic fibrosis (CF) patients, chronic airway infection by Pseudomonas leads to progressive lung destruction ultimately requiring lung transplantation (LT). Following LT, CF-adapted Pseudomonas strains, potentially originating from the sinuses, may seed the allograft leading to infections and reduced allograft survival. We investigated whether CF-adapted Pseudomonas populations invade the donor microbiota and adapt to the non-CF allograft. We collected sequential Pseudomonas isolates and airway samples from a CF-lung transplant recipient during two years, and followed the dynamics of the microbiota and Pseudomonas populations. We show that Pseudomonas invaded the host microbiota within three days post-LT, in association with a reduction in richness and diversity. A dominant mucoid and hypermutator mutL lineage was replaced after 11 days by non-mucoid strains. Despite antibiotic therapy, Pseudomonas dominated the allograft microbiota until day 95. We observed positive selection of pre-LT variants and the appearance of novel mutations. Phenotypic adaptation resulted in increased biofilm formation and swimming motility capacities. Pseudomonas was replaced after 95 days by a microbiota dominated by Actinobacillus. In conclusion, mucoid Pseudomonas adapted to the CF-lung remained able to invade the allograft. Selection of both pre-existing non-mucoid subpopulations and of novel phenotypic traits suggests rapid adaptation of Pseudomonas to the non-CF allograft. Nature Publishing Group 2017-01-17 /pmc/articles/PMC5240337/ /pubmed/28094327 http://dx.doi.org/10.1038/srep40309 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Beaume, M. Köhler, T. Greub, G. Manuel, O. Aubert, J-D. Baerlocher, L. Farinelli, L. Buckling, A. van Delden, C. Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation |
title | Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation |
title_full | Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation |
title_fullStr | Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation |
title_full_unstemmed | Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation |
title_short | Rapid adaptation drives invasion of airway donor microbiota by Pseudomonas after lung transplantation |
title_sort | rapid adaptation drives invasion of airway donor microbiota by pseudomonas after lung transplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240337/ https://www.ncbi.nlm.nih.gov/pubmed/28094327 http://dx.doi.org/10.1038/srep40309 |
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