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Frequency modulation of a bacterial quorum sensing response

In quorum sensing, bacteria secrete or release small molecules into the environment that, once they reach a certain threshold, trigger a behavioural change in the population. As the concentration of these so-called autoinducers is supposed to reflect population density, they were originally assumed...

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Autores principales: Bettenworth, Vera, van Vliet, Simon, Turkowyd, Bartosz, Bamberger, Annika, Wendt, Heiko, McIntosh, Matthew, Steinchen, Wieland, Endesfelder, Ulrike, Becker, Anke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120067/
https://www.ncbi.nlm.nih.gov/pubmed/35589697
http://dx.doi.org/10.1038/s41467-022-30307-6
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author Bettenworth, Vera
van Vliet, Simon
Turkowyd, Bartosz
Bamberger, Annika
Wendt, Heiko
McIntosh, Matthew
Steinchen, Wieland
Endesfelder, Ulrike
Becker, Anke
author_facet Bettenworth, Vera
van Vliet, Simon
Turkowyd, Bartosz
Bamberger, Annika
Wendt, Heiko
McIntosh, Matthew
Steinchen, Wieland
Endesfelder, Ulrike
Becker, Anke
author_sort Bettenworth, Vera
collection PubMed
description In quorum sensing, bacteria secrete or release small molecules into the environment that, once they reach a certain threshold, trigger a behavioural change in the population. As the concentration of these so-called autoinducers is supposed to reflect population density, they were originally assumed to be continuously produced by all cells in a population. However, here we show that in the α-proteobacterium Sinorhizobium meliloti expression of the autoinducer synthase gene is realized in asynchronous stochastic pulses that result from scarcity and, presumably, low binding affinity of the key activator. Physiological cues modulate pulse frequency, and pulse frequency in turn modulates the velocity with which autoinducer levels in the environment reach the threshold to trigger the quorum sensing response. We therefore propose that frequency-modulated pulsing in S. meliloti represents the molecular mechanism for a collective decision-making process in which each cell’s physiological state and need for behavioural adaptation is encoded in the pulse frequency with which it expresses the autoinducer synthase gene; the pulse frequencies of all members of the population are then integrated in the common pool of autoinducers, and only once this vote crosses the threshold, the response behaviour is initiated.
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spelling pubmed-91200672022-05-21 Frequency modulation of a bacterial quorum sensing response Bettenworth, Vera van Vliet, Simon Turkowyd, Bartosz Bamberger, Annika Wendt, Heiko McIntosh, Matthew Steinchen, Wieland Endesfelder, Ulrike Becker, Anke Nat Commun Article In quorum sensing, bacteria secrete or release small molecules into the environment that, once they reach a certain threshold, trigger a behavioural change in the population. As the concentration of these so-called autoinducers is supposed to reflect population density, they were originally assumed to be continuously produced by all cells in a population. However, here we show that in the α-proteobacterium Sinorhizobium meliloti expression of the autoinducer synthase gene is realized in asynchronous stochastic pulses that result from scarcity and, presumably, low binding affinity of the key activator. Physiological cues modulate pulse frequency, and pulse frequency in turn modulates the velocity with which autoinducer levels in the environment reach the threshold to trigger the quorum sensing response. We therefore propose that frequency-modulated pulsing in S. meliloti represents the molecular mechanism for a collective decision-making process in which each cell’s physiological state and need for behavioural adaptation is encoded in the pulse frequency with which it expresses the autoinducer synthase gene; the pulse frequencies of all members of the population are then integrated in the common pool of autoinducers, and only once this vote crosses the threshold, the response behaviour is initiated. Nature Publishing Group UK 2022-05-19 /pmc/articles/PMC9120067/ /pubmed/35589697 http://dx.doi.org/10.1038/s41467-022-30307-6 Text en © The Author(s) 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 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
Bettenworth, Vera
van Vliet, Simon
Turkowyd, Bartosz
Bamberger, Annika
Wendt, Heiko
McIntosh, Matthew
Steinchen, Wieland
Endesfelder, Ulrike
Becker, Anke
Frequency modulation of a bacterial quorum sensing response
title Frequency modulation of a bacterial quorum sensing response
title_full Frequency modulation of a bacterial quorum sensing response
title_fullStr Frequency modulation of a bacterial quorum sensing response
title_full_unstemmed Frequency modulation of a bacterial quorum sensing response
title_short Frequency modulation of a bacterial quorum sensing response
title_sort frequency modulation of a bacterial quorum sensing response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120067/
https://www.ncbi.nlm.nih.gov/pubmed/35589697
http://dx.doi.org/10.1038/s41467-022-30307-6
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