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Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel

Multispecies microbial adherent communities are widespread in nature and organisms, although the principles of their assembly and development remain unclear. Here, we test the possibility of establishing a simplified but relevant model of multispecies biofilm in a non-invasive laboratory setup for t...

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Autores principales: Monmeyran, A., Benyoussef, W., Thomen, P., Dahmane, N., Baliarda, A., Jules, M., Aymerich, S., Henry, N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342524/
https://www.ncbi.nlm.nih.gov/pubmed/34354076
http://dx.doi.org/10.1038/s41522-021-00233-4
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author Monmeyran, A.
Benyoussef, W.
Thomen, P.
Dahmane, N.
Baliarda, A.
Jules, M.
Aymerich, S.
Henry, N.
author_facet Monmeyran, A.
Benyoussef, W.
Thomen, P.
Dahmane, N.
Baliarda, A.
Jules, M.
Aymerich, S.
Henry, N.
author_sort Monmeyran, A.
collection PubMed
description Multispecies microbial adherent communities are widespread in nature and organisms, although the principles of their assembly and development remain unclear. Here, we test the possibility of establishing a simplified but relevant model of multispecies biofilm in a non-invasive laboratory setup for the real-time monitoring of community development. We demonstrate that the four chosen species (Bacillus thuringiensis, Pseudomonas fluorescens, Kocuria varians, and Rhodocyclus sp.) form a dynamic community that deterministically reaches its equilibrium after ~30 h of growth. We reveal the emergence of complexity in this simplified community as reported by an increase in spatial heterogeneity and non-monotonic developmental kinetics. Importantly, we find interspecies interactions consisting of competition for resources—particularly oxygen—and both direct and indirect physical interactions. The simplified experimental model opens new avenues to the study of adherent bacterial communities and their behavior in the context of rapid global change.
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spelling pubmed-83425242021-08-20 Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel Monmeyran, A. Benyoussef, W. Thomen, P. Dahmane, N. Baliarda, A. Jules, M. Aymerich, S. Henry, N. NPJ Biofilms Microbiomes Article Multispecies microbial adherent communities are widespread in nature and organisms, although the principles of their assembly and development remain unclear. Here, we test the possibility of establishing a simplified but relevant model of multispecies biofilm in a non-invasive laboratory setup for the real-time monitoring of community development. We demonstrate that the four chosen species (Bacillus thuringiensis, Pseudomonas fluorescens, Kocuria varians, and Rhodocyclus sp.) form a dynamic community that deterministically reaches its equilibrium after ~30 h of growth. We reveal the emergence of complexity in this simplified community as reported by an increase in spatial heterogeneity and non-monotonic developmental kinetics. Importantly, we find interspecies interactions consisting of competition for resources—particularly oxygen—and both direct and indirect physical interactions. The simplified experimental model opens new avenues to the study of adherent bacterial communities and their behavior in the context of rapid global change. Nature Publishing Group UK 2021-08-05 /pmc/articles/PMC8342524/ /pubmed/34354076 http://dx.doi.org/10.1038/s41522-021-00233-4 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 Article
Monmeyran, A.
Benyoussef, W.
Thomen, P.
Dahmane, N.
Baliarda, A.
Jules, M.
Aymerich, S.
Henry, N.
Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel
title Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel
title_full Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel
title_fullStr Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel
title_full_unstemmed Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel
title_short Four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel
title_sort four species of bacteria deterministically assemble to form a stable biofilm in a millifluidic channel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342524/
https://www.ncbi.nlm.nih.gov/pubmed/34354076
http://dx.doi.org/10.1038/s41522-021-00233-4
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