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Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy
Bacteria commonly form dense biofilms encased in extracellular polymeric substances (EPS). Biofilms are often extremely tolerant to antimicrobials but their reliance on shared EPS may also be a weakness as social evolution theory predicts that inhibiting shared traits can select against resistance....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952394/ https://www.ncbi.nlm.nih.gov/pubmed/31919364 http://dx.doi.org/10.1038/s41467-019-13660-x |
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author | Dieltjens, Lise Appermans, Kenny Lissens, Maries Lories, Bram Kim, Wook Van der Eycken, Erik V. Foster, Kevin R. Steenackers, Hans P. |
author_facet | Dieltjens, Lise Appermans, Kenny Lissens, Maries Lories, Bram Kim, Wook Van der Eycken, Erik V. Foster, Kevin R. Steenackers, Hans P. |
author_sort | Dieltjens, Lise |
collection | PubMed |
description | Bacteria commonly form dense biofilms encased in extracellular polymeric substances (EPS). Biofilms are often extremely tolerant to antimicrobials but their reliance on shared EPS may also be a weakness as social evolution theory predicts that inhibiting shared traits can select against resistance. Here we show that EPS of Salmonella biofilms is a cooperative trait whose benefit is shared among cells, and that EPS inhibition reduces both cell attachment and antimicrobial tolerance. We then compare an EPS inhibitor to conventional antimicrobials in an evolutionary experiment. While resistance against conventional antimicrobials rapidly evolves, we see no evolution of resistance to EPS inhibition. We further show that a resistant strain is outcompeted by a susceptible strain under EPS inhibitor treatment, explaining why resistance does not evolve. Our work suggests that targeting cooperative traits is a viable solution to the problem of antimicrobial resistance. |
format | Online Article Text |
id | pubmed-6952394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69523942020-01-13 Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy Dieltjens, Lise Appermans, Kenny Lissens, Maries Lories, Bram Kim, Wook Van der Eycken, Erik V. Foster, Kevin R. Steenackers, Hans P. Nat Commun Article Bacteria commonly form dense biofilms encased in extracellular polymeric substances (EPS). Biofilms are often extremely tolerant to antimicrobials but their reliance on shared EPS may also be a weakness as social evolution theory predicts that inhibiting shared traits can select against resistance. Here we show that EPS of Salmonella biofilms is a cooperative trait whose benefit is shared among cells, and that EPS inhibition reduces both cell attachment and antimicrobial tolerance. We then compare an EPS inhibitor to conventional antimicrobials in an evolutionary experiment. While resistance against conventional antimicrobials rapidly evolves, we see no evolution of resistance to EPS inhibition. We further show that a resistant strain is outcompeted by a susceptible strain under EPS inhibitor treatment, explaining why resistance does not evolve. Our work suggests that targeting cooperative traits is a viable solution to the problem of antimicrobial resistance. Nature Publishing Group UK 2020-01-09 /pmc/articles/PMC6952394/ /pubmed/31919364 http://dx.doi.org/10.1038/s41467-019-13660-x Text en © The Author(s) 2020 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 Dieltjens, Lise Appermans, Kenny Lissens, Maries Lories, Bram Kim, Wook Van der Eycken, Erik V. Foster, Kevin R. Steenackers, Hans P. Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy |
title | Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy |
title_full | Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy |
title_fullStr | Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy |
title_full_unstemmed | Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy |
title_short | Inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy |
title_sort | inhibiting bacterial cooperation is an evolutionarily robust anti-biofilm strategy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952394/ https://www.ncbi.nlm.nih.gov/pubmed/31919364 http://dx.doi.org/10.1038/s41467-019-13660-x |
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