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Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture
In the wild, bacteria are most frequently found in the form of multicellular structures called biofilms. Biofilms grow at the surface of abiotic and living materials with wide-ranging mechanical properties. The opportunistic pathogen Pseudomonas aeruginosa forms biofilms on indwelling medical device...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127718/ https://www.ncbi.nlm.nih.gov/pubmed/36786569 http://dx.doi.org/10.1128/mbio.03518-22 |
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author | Cont, Alice Vermeil, Joseph Persat, Alexandre |
author_facet | Cont, Alice Vermeil, Joseph Persat, Alexandre |
author_sort | Cont, Alice |
collection | PubMed |
description | In the wild, bacteria are most frequently found in the form of multicellular structures called biofilms. Biofilms grow at the surface of abiotic and living materials with wide-ranging mechanical properties. The opportunistic pathogen Pseudomonas aeruginosa forms biofilms on indwelling medical devices and on soft tissues, including burn wounds and the airway mucosa. Despite the critical role of substrates in the foundation of biofilms, we still lack a clear understanding of how material mechanics regulate their architecture and the physiology of resident bacteria. Here, we demonstrate that physical properties of hydrogel material substrates define P. aeruginosa biofilm architecture. We show that hydrogel mesh size regulates twitching motility, a surface exploration mechanism priming biofilms, ultimately controlling the organization of single cells in the multicellular community. The resulting architectural transitions increase P. aeruginosa’s tolerance to colistin, a last-resort antibiotic. In addition, mechanical regulation of twitching motility affects P. aeruginosa clonal lineages, so that biofilms are more mixed on relatively denser materials. Our results thereby establish material properties as a factor that dramatically affects biofilm architecture, antibiotic efficacy, and evolution of the resident population. |
format | Online Article Text |
id | pubmed-10127718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101277182023-04-26 Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture Cont, Alice Vermeil, Joseph Persat, Alexandre mBio Research Article In the wild, bacteria are most frequently found in the form of multicellular structures called biofilms. Biofilms grow at the surface of abiotic and living materials with wide-ranging mechanical properties. The opportunistic pathogen Pseudomonas aeruginosa forms biofilms on indwelling medical devices and on soft tissues, including burn wounds and the airway mucosa. Despite the critical role of substrates in the foundation of biofilms, we still lack a clear understanding of how material mechanics regulate their architecture and the physiology of resident bacteria. Here, we demonstrate that physical properties of hydrogel material substrates define P. aeruginosa biofilm architecture. We show that hydrogel mesh size regulates twitching motility, a surface exploration mechanism priming biofilms, ultimately controlling the organization of single cells in the multicellular community. The resulting architectural transitions increase P. aeruginosa’s tolerance to colistin, a last-resort antibiotic. In addition, mechanical regulation of twitching motility affects P. aeruginosa clonal lineages, so that biofilms are more mixed on relatively denser materials. Our results thereby establish material properties as a factor that dramatically affects biofilm architecture, antibiotic efficacy, and evolution of the resident population. American Society for Microbiology 2023-02-14 /pmc/articles/PMC10127718/ /pubmed/36786569 http://dx.doi.org/10.1128/mbio.03518-22 Text en Copyright © 2023 Cont et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Cont, Alice Vermeil, Joseph Persat, Alexandre Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture |
title | Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture |
title_full | Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture |
title_fullStr | Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture |
title_full_unstemmed | Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture |
title_short | Material Substrate Physical Properties Control Pseudomonas aeruginosa Biofilm Architecture |
title_sort | material substrate physical properties control pseudomonas aeruginosa biofilm architecture |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127718/ https://www.ncbi.nlm.nih.gov/pubmed/36786569 http://dx.doi.org/10.1128/mbio.03518-22 |
work_keys_str_mv | AT contalice materialsubstratephysicalpropertiescontrolpseudomonasaeruginosabiofilmarchitecture AT vermeiljoseph materialsubstratephysicalpropertiescontrolpseudomonasaeruginosabiofilmarchitecture AT persatalexandre materialsubstratephysicalpropertiescontrolpseudomonasaeruginosabiofilmarchitecture |