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Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity
Quorum-sensing bacteria in a growing colony of cells send out signalling molecules (so-called “autoinducers”) and themselves sense the autoinducer concentration in their vicinity. Once—due to increased local cell density inside a “cluster” of the growing colony—the concentration of autoinducers exce...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700081/ https://www.ncbi.nlm.nih.gov/pubmed/31427659 http://dx.doi.org/10.1038/s41598-019-48525-2 |
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author | Kindler, Oliver Pulkkinen, Otto Cherstvy, Andrey G. Metzler, Ralf |
author_facet | Kindler, Oliver Pulkkinen, Otto Cherstvy, Andrey G. Metzler, Ralf |
author_sort | Kindler, Oliver |
collection | PubMed |
description | Quorum-sensing bacteria in a growing colony of cells send out signalling molecules (so-called “autoinducers”) and themselves sense the autoinducer concentration in their vicinity. Once—due to increased local cell density inside a “cluster” of the growing colony—the concentration of autoinducers exceeds a threshold value, cells in this clusters get “induced” into a communal, multi-cell biofilm-forming mode in a cluster-wide burst event. We analyse quantitatively the influence of spatial disorder, the local heterogeneity of the spatial distribution of cells in the colony, and additional physical parameters such as the autoinducer signal range on the induction dynamics of the cell colony. Spatial inhomogeneity with higher local cell concentrations in clusters leads to earlier but more localised induction events, while homogeneous distributions lead to comparatively delayed but more concerted induction of the cell colony, and, thus, a behaviour close to the mean-field dynamics. We quantify the induction dynamics with quantifiers such as the time series of induction events and burst sizes, the grouping into induction families, and the mean autoinducer concentration levels. Consequences for different scenarios of biofilm growth are discussed, providing possible cues for biofilm control in both health care and biotechnology. |
format | Online Article Text |
id | pubmed-6700081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67000812019-08-21 Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity Kindler, Oliver Pulkkinen, Otto Cherstvy, Andrey G. Metzler, Ralf Sci Rep Article Quorum-sensing bacteria in a growing colony of cells send out signalling molecules (so-called “autoinducers”) and themselves sense the autoinducer concentration in their vicinity. Once—due to increased local cell density inside a “cluster” of the growing colony—the concentration of autoinducers exceeds a threshold value, cells in this clusters get “induced” into a communal, multi-cell biofilm-forming mode in a cluster-wide burst event. We analyse quantitatively the influence of spatial disorder, the local heterogeneity of the spatial distribution of cells in the colony, and additional physical parameters such as the autoinducer signal range on the induction dynamics of the cell colony. Spatial inhomogeneity with higher local cell concentrations in clusters leads to earlier but more localised induction events, while homogeneous distributions lead to comparatively delayed but more concerted induction of the cell colony, and, thus, a behaviour close to the mean-field dynamics. We quantify the induction dynamics with quantifiers such as the time series of induction events and burst sizes, the grouping into induction families, and the mean autoinducer concentration levels. Consequences for different scenarios of biofilm growth are discussed, providing possible cues for biofilm control in both health care and biotechnology. Nature Publishing Group UK 2019-08-19 /pmc/articles/PMC6700081/ /pubmed/31427659 http://dx.doi.org/10.1038/s41598-019-48525-2 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Kindler, Oliver Pulkkinen, Otto Cherstvy, Andrey G. Metzler, Ralf Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity |
title | Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity |
title_full | Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity |
title_fullStr | Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity |
title_full_unstemmed | Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity |
title_short | Burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity |
title_sort | burst statistics in an early biofilm quorum sensing model: the role of spatial colony-growth heterogeneity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700081/ https://www.ncbi.nlm.nih.gov/pubmed/31427659 http://dx.doi.org/10.1038/s41598-019-48525-2 |
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