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Human-associated microbiota suppress invading bacteria even under disruption by antibiotics
In light of their adverse impacts on resident microbial communities, it is widely predicted that broad-spectrum antibiotics can promote the spread of resistance by releasing resistant strains from competition with other strains and species. We investigated the competitive suppression of a resistant...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397715/ https://www.ncbi.nlm.nih.gov/pubmed/33712700 http://dx.doi.org/10.1038/s41396-021-00929-7 |
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author | Letten, Andrew D. Baumgartner, Michael Pfrunder-Cardozo, Katia R. Levine, Jonathan M. Hall, Alex R. |
author_facet | Letten, Andrew D. Baumgartner, Michael Pfrunder-Cardozo, Katia R. Levine, Jonathan M. Hall, Alex R. |
author_sort | Letten, Andrew D. |
collection | PubMed |
description | In light of their adverse impacts on resident microbial communities, it is widely predicted that broad-spectrum antibiotics can promote the spread of resistance by releasing resistant strains from competition with other strains and species. We investigated the competitive suppression of a resistant strain of Escherichia coli inoculated into human-associated communities in the presence and absence of the broad and narrow spectrum antibiotics rifampicin and polymyxin B, respectively. We found strong evidence of community-level suppression of the resistant strain in the absence of antibiotics and, despite large changes in community composition and abundance following rifampicin exposure, suppression of the invading resistant strain was maintained in both antibiotic treatments. Instead, the strength of competitive suppression was more strongly associated with the source community (stool sample from individual human donor). This suggests microbiome composition strongly influences the competitive suppression of antibiotic-resistant strains, but at least some antibiotic-associated disruption can be tolerated before competitive release is observed. A deeper understanding of this association will aid the development of ecologically-aware strategies for managing antibiotic resistance. |
format | Online Article Text |
id | pubmed-8397715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83977152021-09-15 Human-associated microbiota suppress invading bacteria even under disruption by antibiotics Letten, Andrew D. Baumgartner, Michael Pfrunder-Cardozo, Katia R. Levine, Jonathan M. Hall, Alex R. ISME J Brief Communication In light of their adverse impacts on resident microbial communities, it is widely predicted that broad-spectrum antibiotics can promote the spread of resistance by releasing resistant strains from competition with other strains and species. We investigated the competitive suppression of a resistant strain of Escherichia coli inoculated into human-associated communities in the presence and absence of the broad and narrow spectrum antibiotics rifampicin and polymyxin B, respectively. We found strong evidence of community-level suppression of the resistant strain in the absence of antibiotics and, despite large changes in community composition and abundance following rifampicin exposure, suppression of the invading resistant strain was maintained in both antibiotic treatments. Instead, the strength of competitive suppression was more strongly associated with the source community (stool sample from individual human donor). This suggests microbiome composition strongly influences the competitive suppression of antibiotic-resistant strains, but at least some antibiotic-associated disruption can be tolerated before competitive release is observed. A deeper understanding of this association will aid the development of ecologically-aware strategies for managing antibiotic resistance. Nature Publishing Group UK 2021-03-12 2021-09 /pmc/articles/PMC8397715/ /pubmed/33712700 http://dx.doi.org/10.1038/s41396-021-00929-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Communication Letten, Andrew D. Baumgartner, Michael Pfrunder-Cardozo, Katia R. Levine, Jonathan M. Hall, Alex R. Human-associated microbiota suppress invading bacteria even under disruption by antibiotics |
title | Human-associated microbiota suppress invading bacteria even under disruption by antibiotics |
title_full | Human-associated microbiota suppress invading bacteria even under disruption by antibiotics |
title_fullStr | Human-associated microbiota suppress invading bacteria even under disruption by antibiotics |
title_full_unstemmed | Human-associated microbiota suppress invading bacteria even under disruption by antibiotics |
title_short | Human-associated microbiota suppress invading bacteria even under disruption by antibiotics |
title_sort | human-associated microbiota suppress invading bacteria even under disruption by antibiotics |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397715/ https://www.ncbi.nlm.nih.gov/pubmed/33712700 http://dx.doi.org/10.1038/s41396-021-00929-7 |
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