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Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing

Bacterial communities attached to surfaces under fluid flow represent a widespread lifestyle of the microbial world. Through shear stress generation and molecular transport regulation, hydrodynamics conveys effects that are very different by nature but strongly coupled. To decipher the influence of...

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Autores principales: Thomen, Philippe, Robert, Jérôme, Monmeyran, Amaury, Bitbol, Anne-Florence, Douarche, Carine, Henry, Nelly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389662/
https://www.ncbi.nlm.nih.gov/pubmed/28403171
http://dx.doi.org/10.1371/journal.pone.0175197
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author Thomen, Philippe
Robert, Jérôme
Monmeyran, Amaury
Bitbol, Anne-Florence
Douarche, Carine
Henry, Nelly
author_facet Thomen, Philippe
Robert, Jérôme
Monmeyran, Amaury
Bitbol, Anne-Florence
Douarche, Carine
Henry, Nelly
author_sort Thomen, Philippe
collection PubMed
description Bacterial communities attached to surfaces under fluid flow represent a widespread lifestyle of the microbial world. Through shear stress generation and molecular transport regulation, hydrodynamics conveys effects that are very different by nature but strongly coupled. To decipher the influence of these levers on bacterial biofilms immersed in moving fluids, we quantitatively and simultaneously investigated physicochemical and biological properties of the biofilm. We designed a millifluidic setup allowing to control hydrodynamic conditions and to monitor biofilm development in real time using microscope imaging. We also conducted a transcriptomic analysis to detect a potential physiological response to hydrodynamics. We discovered that a threshold value of shear stress determined biofilm settlement, with sub-piconewton forces sufficient to prevent biofilm initiation. As a consequence, distinct hydrodynamic conditions, which set spatial distribution of shear stress, promoted distinct colonization patterns with consequences on the growth mode. However, no direct impact of mechanical forces on biofilm growth rate was observed. Consistently, no mechanosensing gene emerged from our differential transcriptomic analysis comparing distinct hydrodynamic conditions. Instead, we found that hydrodynamic molecular transport crucially impacts biofilm growth by controlling oxygen availability. Our results shed light on biofilm response to hydrodynamics and open new avenues to achieve informed design of fluidic setups for investigating, engineering or fighting adherent communities.
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spelling pubmed-53896622017-05-03 Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing Thomen, Philippe Robert, Jérôme Monmeyran, Amaury Bitbol, Anne-Florence Douarche, Carine Henry, Nelly PLoS One Research Article Bacterial communities attached to surfaces under fluid flow represent a widespread lifestyle of the microbial world. Through shear stress generation and molecular transport regulation, hydrodynamics conveys effects that are very different by nature but strongly coupled. To decipher the influence of these levers on bacterial biofilms immersed in moving fluids, we quantitatively and simultaneously investigated physicochemical and biological properties of the biofilm. We designed a millifluidic setup allowing to control hydrodynamic conditions and to monitor biofilm development in real time using microscope imaging. We also conducted a transcriptomic analysis to detect a potential physiological response to hydrodynamics. We discovered that a threshold value of shear stress determined biofilm settlement, with sub-piconewton forces sufficient to prevent biofilm initiation. As a consequence, distinct hydrodynamic conditions, which set spatial distribution of shear stress, promoted distinct colonization patterns with consequences on the growth mode. However, no direct impact of mechanical forces on biofilm growth rate was observed. Consistently, no mechanosensing gene emerged from our differential transcriptomic analysis comparing distinct hydrodynamic conditions. Instead, we found that hydrodynamic molecular transport crucially impacts biofilm growth by controlling oxygen availability. Our results shed light on biofilm response to hydrodynamics and open new avenues to achieve informed design of fluidic setups for investigating, engineering or fighting adherent communities. Public Library of Science 2017-04-12 /pmc/articles/PMC5389662/ /pubmed/28403171 http://dx.doi.org/10.1371/journal.pone.0175197 Text en © 2017 Thomen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Thomen, Philippe
Robert, Jérôme
Monmeyran, Amaury
Bitbol, Anne-Florence
Douarche, Carine
Henry, Nelly
Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing
title Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing
title_full Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing
title_fullStr Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing
title_full_unstemmed Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing
title_short Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing
title_sort bacterial biofilm under flow: first a physical struggle to stay, then a matter of breathing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389662/
https://www.ncbi.nlm.nih.gov/pubmed/28403171
http://dx.doi.org/10.1371/journal.pone.0175197
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