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A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm

Biofilms are complex communities of bacteria that exhibit a variety of collective behaviors. These behaviors improve their ability to survive in many different environments. One of these collective behaviors seen in Bacillus subtilis is the ability for starving cells to stop the growth of other cell...

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Autores principales: Ford, Noah, Fisher, Garth, Prindle, Arthur, Chopp, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857140/
https://www.ncbi.nlm.nih.gov/pubmed/33856558
http://dx.doi.org/10.1007/s11538-021-00887-3
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author Ford, Noah
Fisher, Garth
Prindle, Arthur
Chopp, David
author_facet Ford, Noah
Fisher, Garth
Prindle, Arthur
Chopp, David
author_sort Ford, Noah
collection PubMed
description Biofilms are complex communities of bacteria that exhibit a variety of collective behaviors. These behaviors improve their ability to survive in many different environments. One of these collective behaviors seen in Bacillus subtilis is the ability for starving cells to stop the growth of other cells using potassium signaling and voltage changes. This signaling produces an oscillatory growth pattern so that during periods of low growth the nutrients diffuse deeper into the biofilm and reach the nutrient-starved, interior regions of the biomass. In this paper, we develop a mathematical model to describe this oscillatory behavior, and we use this model to develop a two-dimensional simulation that reproduces many of the important features seen in the experimental data. This simulation allows us to examine the spatial patterning of the oscillatory behavior to better understand the relationships between the various regions of the biofilm. Studying the spatial components of the metabolic and voltage oscillations could allow for the development of new control techniques for biofilms with complex shapes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11538-021-00887-3.
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spelling pubmed-88571402022-02-23 A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm Ford, Noah Fisher, Garth Prindle, Arthur Chopp, David Bull Math Biol Original Article Biofilms are complex communities of bacteria that exhibit a variety of collective behaviors. These behaviors improve their ability to survive in many different environments. One of these collective behaviors seen in Bacillus subtilis is the ability for starving cells to stop the growth of other cells using potassium signaling and voltage changes. This signaling produces an oscillatory growth pattern so that during periods of low growth the nutrients diffuse deeper into the biofilm and reach the nutrient-starved, interior regions of the biomass. In this paper, we develop a mathematical model to describe this oscillatory behavior, and we use this model to develop a two-dimensional simulation that reproduces many of the important features seen in the experimental data. This simulation allows us to examine the spatial patterning of the oscillatory behavior to better understand the relationships between the various regions of the biofilm. Studying the spatial components of the metabolic and voltage oscillations could allow for the development of new control techniques for biofilms with complex shapes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11538-021-00887-3. Springer US 2021-04-15 2021 /pmc/articles/PMC8857140/ /pubmed/33856558 http://dx.doi.org/10.1007/s11538-021-00887-3 Text en © The Author(s) 2021, corrected publication 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Ford, Noah
Fisher, Garth
Prindle, Arthur
Chopp, David
A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm
title A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm
title_full A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm
title_fullStr A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm
title_full_unstemmed A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm
title_short A Two-Dimensional Model of Potassium Signaling and Oscillatory Growth in a Biofilm
title_sort two-dimensional model of potassium signaling and oscillatory growth in a biofilm
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857140/
https://www.ncbi.nlm.nih.gov/pubmed/33856558
http://dx.doi.org/10.1007/s11538-021-00887-3
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