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The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital

The biological features that allow a pathogen to survive in the hospital environment are mostly unknown. The extinction of bacterial epidemics in hospitals is mostly attributed to changes in medical practice, including infection control, but the role of bacterial adaptation has never been documented...

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Autores principales: Petitjean, Marie, Juarez, Paulo, Meunier, Alexandre, Daguindau, Etienne, Puja, Hélène, Bertrand, Xavier, Valot, Benoit, Hocquet, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715434/
https://www.ncbi.nlm.nih.gov/pubmed/34473016
http://dx.doi.org/10.1099/mgen.0.000629
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author Petitjean, Marie
Juarez, Paulo
Meunier, Alexandre
Daguindau, Etienne
Puja, Hélène
Bertrand, Xavier
Valot, Benoit
Hocquet, Didier
author_facet Petitjean, Marie
Juarez, Paulo
Meunier, Alexandre
Daguindau, Etienne
Puja, Hélène
Bertrand, Xavier
Valot, Benoit
Hocquet, Didier
author_sort Petitjean, Marie
collection PubMed
description The biological features that allow a pathogen to survive in the hospital environment are mostly unknown. The extinction of bacterial epidemics in hospitals is mostly attributed to changes in medical practice, including infection control, but the role of bacterial adaptation has never been documented. We analysed a collection of Pseudomonas aeruginosa isolates belonging to the Besançon Epidemic Strain (BES), responsible for a 12year nosocomial outbreak, using a genotype-to-phenotype approach. Bayesian analysis estimated the emergence of the clone in the hospital 5 years before its opening, during the creation of its water distribution network made of copper. BES survived better than the reference strains PAO1 and PA14 in a copper solution due to a genomic island containing 13 metal-resistance genes and was specifically able to proliferate in the ubiquitous amoeba Vermamoeba vermiformis. Mutations affecting amino-acid metabolism, antibiotic resistance, lipopolysaccharide biosynthesis, and regulation were enriched during the spread of BES. Seven distinct regulatory mutations attenuated the overexpression of the genes encoding the efflux pump MexAB-OprM over time. The fitness of BES decreased over time in correlation with its genome size. Overall, the resistance to inhibitors and predators presumably aided the proliferation and propagation of BES in the plumbing system of the hospital. The pathogen further spread among patients via multiple routes of contamination. The decreased prevalence of patients infected by BES mirrored the parallel and convergent genomic evolution and reduction that affected bacterial fitness. Along with infection control measures, this may have participated in the extinction of BES in the hospital setting.
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spelling pubmed-87154342021-12-29 The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital Petitjean, Marie Juarez, Paulo Meunier, Alexandre Daguindau, Etienne Puja, Hélène Bertrand, Xavier Valot, Benoit Hocquet, Didier Microb Genom Research Articles The biological features that allow a pathogen to survive in the hospital environment are mostly unknown. The extinction of bacterial epidemics in hospitals is mostly attributed to changes in medical practice, including infection control, but the role of bacterial adaptation has never been documented. We analysed a collection of Pseudomonas aeruginosa isolates belonging to the Besançon Epidemic Strain (BES), responsible for a 12year nosocomial outbreak, using a genotype-to-phenotype approach. Bayesian analysis estimated the emergence of the clone in the hospital 5 years before its opening, during the creation of its water distribution network made of copper. BES survived better than the reference strains PAO1 and PA14 in a copper solution due to a genomic island containing 13 metal-resistance genes and was specifically able to proliferate in the ubiquitous amoeba Vermamoeba vermiformis. Mutations affecting amino-acid metabolism, antibiotic resistance, lipopolysaccharide biosynthesis, and regulation were enriched during the spread of BES. Seven distinct regulatory mutations attenuated the overexpression of the genes encoding the efflux pump MexAB-OprM over time. The fitness of BES decreased over time in correlation with its genome size. Overall, the resistance to inhibitors and predators presumably aided the proliferation and propagation of BES in the plumbing system of the hospital. The pathogen further spread among patients via multiple routes of contamination. The decreased prevalence of patients infected by BES mirrored the parallel and convergent genomic evolution and reduction that affected bacterial fitness. Along with infection control measures, this may have participated in the extinction of BES in the hospital setting. Microbiology Society 2021-09-02 /pmc/articles/PMC8715434/ /pubmed/34473016 http://dx.doi.org/10.1099/mgen.0.000629 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License.
spellingShingle Research Articles
Petitjean, Marie
Juarez, Paulo
Meunier, Alexandre
Daguindau, Etienne
Puja, Hélène
Bertrand, Xavier
Valot, Benoit
Hocquet, Didier
The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital
title The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital
title_full The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital
title_fullStr The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital
title_full_unstemmed The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital
title_short The rise and the fall of a Pseudomonas aeruginosa endemic lineage in a hospital
title_sort rise and the fall of a pseudomonas aeruginosa endemic lineage in a hospital
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715434/
https://www.ncbi.nlm.nih.gov/pubmed/34473016
http://dx.doi.org/10.1099/mgen.0.000629
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