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A biophysical limit for quorum sensing in biofilms

Bacteria grow on surfaces in complex immobile communities known as biofilms, which are composed of cells embedded in an extracellular matrix. Within biofilms, bacteria often interact with members of their own species and cooperate or compete with members of other species via quorum sensing (QS). QS...

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Autores principales: Narla, Avaneesh V., Borenstein, David Bruce, Wingreen, Ned S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166027/
https://www.ncbi.nlm.nih.gov/pubmed/34006640
http://dx.doi.org/10.1073/pnas.2022818118
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author Narla, Avaneesh V.
Borenstein, David Bruce
Wingreen, Ned S.
author_facet Narla, Avaneesh V.
Borenstein, David Bruce
Wingreen, Ned S.
author_sort Narla, Avaneesh V.
collection PubMed
description Bacteria grow on surfaces in complex immobile communities known as biofilms, which are composed of cells embedded in an extracellular matrix. Within biofilms, bacteria often interact with members of their own species and cooperate or compete with members of other species via quorum sensing (QS). QS is a process by which microbes produce, secrete, and subsequently detect small molecules called autoinducers (AIs) to assess their local population density. We explore the competitive advantage of QS through agent-based simulations of a spatial model in which colony expansion via extracellular matrix production provides greater access to a limiting diffusible nutrient. We note a significant difference in results based on whether AI production is constitutive or limited by nutrient availability: If AI production is constitutive, simple QS-based matrix-production strategies can be far superior to any fixed strategy. However, if AI production is limited by nutrient availability, QS-based strategies fail to provide a significant advantage over fixed strategies. To explain this dichotomy, we derive a biophysical limit for the dynamic range of nutrient-limited AI concentrations in biofilms. This range is remarkably small (less than 10-fold) for the realistic case in which a growth-limiting diffusible nutrient is taken up within a narrow active growth layer. This biophysical limit implies that for QS to be most effective in biofilms AI production should be a protected function not directly tied to metabolism.
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spelling pubmed-81660272021-06-10 A biophysical limit for quorum sensing in biofilms Narla, Avaneesh V. Borenstein, David Bruce Wingreen, Ned S. Proc Natl Acad Sci U S A Biological Sciences Bacteria grow on surfaces in complex immobile communities known as biofilms, which are composed of cells embedded in an extracellular matrix. Within biofilms, bacteria often interact with members of their own species and cooperate or compete with members of other species via quorum sensing (QS). QS is a process by which microbes produce, secrete, and subsequently detect small molecules called autoinducers (AIs) to assess their local population density. We explore the competitive advantage of QS through agent-based simulations of a spatial model in which colony expansion via extracellular matrix production provides greater access to a limiting diffusible nutrient. We note a significant difference in results based on whether AI production is constitutive or limited by nutrient availability: If AI production is constitutive, simple QS-based matrix-production strategies can be far superior to any fixed strategy. However, if AI production is limited by nutrient availability, QS-based strategies fail to provide a significant advantage over fixed strategies. To explain this dichotomy, we derive a biophysical limit for the dynamic range of nutrient-limited AI concentrations in biofilms. This range is remarkably small (less than 10-fold) for the realistic case in which a growth-limiting diffusible nutrient is taken up within a narrow active growth layer. This biophysical limit implies that for QS to be most effective in biofilms AI production should be a protected function not directly tied to metabolism. National Academy of Sciences 2021-05-25 2021-05-18 /pmc/articles/PMC8166027/ /pubmed/34006640 http://dx.doi.org/10.1073/pnas.2022818118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Narla, Avaneesh V.
Borenstein, David Bruce
Wingreen, Ned S.
A biophysical limit for quorum sensing in biofilms
title A biophysical limit for quorum sensing in biofilms
title_full A biophysical limit for quorum sensing in biofilms
title_fullStr A biophysical limit for quorum sensing in biofilms
title_full_unstemmed A biophysical limit for quorum sensing in biofilms
title_short A biophysical limit for quorum sensing in biofilms
title_sort biophysical limit for quorum sensing in biofilms
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166027/
https://www.ncbi.nlm.nih.gov/pubmed/34006640
http://dx.doi.org/10.1073/pnas.2022818118
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