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Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases
BACKGROUND: The prevalence of extended beta-lactamase producing Enterobacteriaceae (ESBL-E) has been constantly increasing over the last few decades. These microorganisms that have acquired broad antibiotic resistance are now common human pathogens. Changes in the gut microbiome, induced by antibiot...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359458/ https://www.ncbi.nlm.nih.gov/pubmed/32665016 http://dx.doi.org/10.1186/s13756-020-00773-y |
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author | Le Bastard, Quentin Chapelet, Guillaume Birgand, Gabriel Hillmann, Benjamin M. Javaudin, François Hayatgheib, Niki Bourigault, Céline Bemer, Pascale De Decker, Laure Batard, Eric Lepelletier, Didier Montassier, Emmanuel |
author_facet | Le Bastard, Quentin Chapelet, Guillaume Birgand, Gabriel Hillmann, Benjamin M. Javaudin, François Hayatgheib, Niki Bourigault, Céline Bemer, Pascale De Decker, Laure Batard, Eric Lepelletier, Didier Montassier, Emmanuel |
author_sort | Le Bastard, Quentin |
collection | PubMed |
description | BACKGROUND: The prevalence of extended beta-lactamase producing Enterobacteriaceae (ESBL-E) has been constantly increasing over the last few decades. These microorganisms that have acquired broad antibiotic resistance are now common human pathogens. Changes in the gut microbiome, induced by antibiotics or other drugs, enable expansion of these microorganisms, but the mechanisms are not yet fully understood. OBJECTIVES: The main objective was to identify specific bacteria and functional pathways and genes characterizing the gut microbiome of nursing home residents carrying ESBL-E, using metagenomics. SUBJECTS AND METHODS: We included 144 residents living in two different nursing homes. All fecal samples were screened for ESBL-E and gut microbiome was characterized using shallow shotgun metagenomic DNA sequencing. RESULTS: Ten nursing home residents were colonized by ESBL-E, namely Escherichia coli, Klebsiella pneumoniae and Enterobacter cloacae species, and were compared to non-carriers. We found that ESBL-E carriers had an alteration in within-sample diversity. Using a bootstrap algorithm, we found that the gut microbiome of ESBL-E carriers was depleted in butyrate-producing species, enriched in succinate-producing species and enriched in pathways involved in intracellular pH homeostasis compared to non-carriers individuals. Several energy metabolism pathways were overrepresented in ESBL-E carriers suggesting a greater ability to metabolize multiple microbiota and mucus layer-derived nutrients. CONCLUSIONS: The gut microbiome of ESBL-E carriers in nursing homes harbors specific taxonomic and functional characteristics, conferring an environment that enables Enterobacteriaceae expansion. Here we describe new functional features associated with ESBL-E carriage that could help us to elucidate the complex interactions leading to colonization persistence in the human gut microbiota. |
format | Online Article Text |
id | pubmed-7359458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73594582020-07-17 Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases Le Bastard, Quentin Chapelet, Guillaume Birgand, Gabriel Hillmann, Benjamin M. Javaudin, François Hayatgheib, Niki Bourigault, Céline Bemer, Pascale De Decker, Laure Batard, Eric Lepelletier, Didier Montassier, Emmanuel Antimicrob Resist Infect Control Research BACKGROUND: The prevalence of extended beta-lactamase producing Enterobacteriaceae (ESBL-E) has been constantly increasing over the last few decades. These microorganisms that have acquired broad antibiotic resistance are now common human pathogens. Changes in the gut microbiome, induced by antibiotics or other drugs, enable expansion of these microorganisms, but the mechanisms are not yet fully understood. OBJECTIVES: The main objective was to identify specific bacteria and functional pathways and genes characterizing the gut microbiome of nursing home residents carrying ESBL-E, using metagenomics. SUBJECTS AND METHODS: We included 144 residents living in two different nursing homes. All fecal samples were screened for ESBL-E and gut microbiome was characterized using shallow shotgun metagenomic DNA sequencing. RESULTS: Ten nursing home residents were colonized by ESBL-E, namely Escherichia coli, Klebsiella pneumoniae and Enterobacter cloacae species, and were compared to non-carriers. We found that ESBL-E carriers had an alteration in within-sample diversity. Using a bootstrap algorithm, we found that the gut microbiome of ESBL-E carriers was depleted in butyrate-producing species, enriched in succinate-producing species and enriched in pathways involved in intracellular pH homeostasis compared to non-carriers individuals. Several energy metabolism pathways were overrepresented in ESBL-E carriers suggesting a greater ability to metabolize multiple microbiota and mucus layer-derived nutrients. CONCLUSIONS: The gut microbiome of ESBL-E carriers in nursing homes harbors specific taxonomic and functional characteristics, conferring an environment that enables Enterobacteriaceae expansion. Here we describe new functional features associated with ESBL-E carriage that could help us to elucidate the complex interactions leading to colonization persistence in the human gut microbiota. BioMed Central 2020-07-14 /pmc/articles/PMC7359458/ /pubmed/32665016 http://dx.doi.org/10.1186/s13756-020-00773-y Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Le Bastard, Quentin Chapelet, Guillaume Birgand, Gabriel Hillmann, Benjamin M. Javaudin, François Hayatgheib, Niki Bourigault, Céline Bemer, Pascale De Decker, Laure Batard, Eric Lepelletier, Didier Montassier, Emmanuel Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases |
title | Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases |
title_full | Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases |
title_fullStr | Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases |
title_full_unstemmed | Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases |
title_short | Gut microbiome signatures of nursing home residents carrying Enterobacteria producing extended-spectrum β-lactamases |
title_sort | gut microbiome signatures of nursing home residents carrying enterobacteria producing extended-spectrum β-lactamases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359458/ https://www.ncbi.nlm.nih.gov/pubmed/32665016 http://dx.doi.org/10.1186/s13756-020-00773-y |
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