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Social Evolution Selects for Redundancy in Bacterial Quorum Sensing

Quorum sensing is a process of chemical communication that bacteria use to monitor cell density and coordinate cooperative behaviors. Quorum sensing relies on extracellular signal molecules and cognate receptor pairs. While a single quorum-sensing system is sufficient to probe cell density, bacteria...

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Autores principales: Even-Tov, Eran, Omer Bendori, Shira, Valastyan, Julie, Ke, Xiaobo, Pollak, Shaul, Bareia, Tasneem, Ben-Zion, Ishay, Bassler, Bonnie L., Eldar, Avigdor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771773/
https://www.ncbi.nlm.nih.gov/pubmed/26927849
http://dx.doi.org/10.1371/journal.pbio.1002386
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author Even-Tov, Eran
Omer Bendori, Shira
Valastyan, Julie
Ke, Xiaobo
Pollak, Shaul
Bareia, Tasneem
Ben-Zion, Ishay
Bassler, Bonnie L.
Eldar, Avigdor
author_facet Even-Tov, Eran
Omer Bendori, Shira
Valastyan, Julie
Ke, Xiaobo
Pollak, Shaul
Bareia, Tasneem
Ben-Zion, Ishay
Bassler, Bonnie L.
Eldar, Avigdor
author_sort Even-Tov, Eran
collection PubMed
description Quorum sensing is a process of chemical communication that bacteria use to monitor cell density and coordinate cooperative behaviors. Quorum sensing relies on extracellular signal molecules and cognate receptor pairs. While a single quorum-sensing system is sufficient to probe cell density, bacteria frequently use multiple quorum-sensing systems to regulate the same cooperative behaviors. The potential benefits of these redundant network structures are not clear. Here, we combine modeling and experimental analyses of the Bacillus subtilis and Vibrio harveyi quorum-sensing networks to show that accumulation of multiple quorum-sensing systems may be driven by a facultative cheating mechanism. We demonstrate that a strain that has acquired an additional quorum-sensing system can exploit its ancestor that possesses one fewer system, but nonetheless, resume full cooperation with its kin when it is fixed in the population. We identify the molecular network design criteria required for this advantage. Our results suggest that increased complexity in bacterial social signaling circuits can evolve without providing an adaptive advantage in a clonal population.
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spelling pubmed-47717732016-03-07 Social Evolution Selects for Redundancy in Bacterial Quorum Sensing Even-Tov, Eran Omer Bendori, Shira Valastyan, Julie Ke, Xiaobo Pollak, Shaul Bareia, Tasneem Ben-Zion, Ishay Bassler, Bonnie L. Eldar, Avigdor PLoS Biol Research Article Quorum sensing is a process of chemical communication that bacteria use to monitor cell density and coordinate cooperative behaviors. Quorum sensing relies on extracellular signal molecules and cognate receptor pairs. While a single quorum-sensing system is sufficient to probe cell density, bacteria frequently use multiple quorum-sensing systems to regulate the same cooperative behaviors. The potential benefits of these redundant network structures are not clear. Here, we combine modeling and experimental analyses of the Bacillus subtilis and Vibrio harveyi quorum-sensing networks to show that accumulation of multiple quorum-sensing systems may be driven by a facultative cheating mechanism. We demonstrate that a strain that has acquired an additional quorum-sensing system can exploit its ancestor that possesses one fewer system, but nonetheless, resume full cooperation with its kin when it is fixed in the population. We identify the molecular network design criteria required for this advantage. Our results suggest that increased complexity in bacterial social signaling circuits can evolve without providing an adaptive advantage in a clonal population. Public Library of Science 2016-02-29 /pmc/articles/PMC4771773/ /pubmed/26927849 http://dx.doi.org/10.1371/journal.pbio.1002386 Text en © 2016 Even-Tov 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Even-Tov, Eran
Omer Bendori, Shira
Valastyan, Julie
Ke, Xiaobo
Pollak, Shaul
Bareia, Tasneem
Ben-Zion, Ishay
Bassler, Bonnie L.
Eldar, Avigdor
Social Evolution Selects for Redundancy in Bacterial Quorum Sensing
title Social Evolution Selects for Redundancy in Bacterial Quorum Sensing
title_full Social Evolution Selects for Redundancy in Bacterial Quorum Sensing
title_fullStr Social Evolution Selects for Redundancy in Bacterial Quorum Sensing
title_full_unstemmed Social Evolution Selects for Redundancy in Bacterial Quorum Sensing
title_short Social Evolution Selects for Redundancy in Bacterial Quorum Sensing
title_sort social evolution selects for redundancy in bacterial quorum sensing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771773/
https://www.ncbi.nlm.nih.gov/pubmed/26927849
http://dx.doi.org/10.1371/journal.pbio.1002386
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