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In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies

Many species of bacteria collectively sense and respond to their social and physical environment via ‘quorum sensing’ (QS), a communication system controlling extracellular cooperative traits. Despite detailed understanding of the mechanisms of signal production and response, there remains considera...

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Autores principales: Wang, Yifei, Rattray, Jennifer B., Thomas, Stephen A., Gurney, James, Brown, Sam P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248119/
https://www.ncbi.nlm.nih.gov/pubmed/32451396
http://dx.doi.org/10.1038/s41598-020-65076-z
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author Wang, Yifei
Rattray, Jennifer B.
Thomas, Stephen A.
Gurney, James
Brown, Sam P.
author_facet Wang, Yifei
Rattray, Jennifer B.
Thomas, Stephen A.
Gurney, James
Brown, Sam P.
author_sort Wang, Yifei
collection PubMed
description Many species of bacteria collectively sense and respond to their social and physical environment via ‘quorum sensing’ (QS), a communication system controlling extracellular cooperative traits. Despite detailed understanding of the mechanisms of signal production and response, there remains considerable debate over the functional role(s) of QS: in short, what is it for? Experimental studies have found support for diverse functional roles: density sensing, mass-transfer sensing, genotype sensing, etc. While consistent with theory, these results cannot separate whether these functions were drivers of QS adaption, or simply artifacts or ‘spandrels’ of systems shaped by distinct ecological pressures. The challenge of separating spandrels from drivers of adaptation is particularly hard to address using extant bacterial species with poorly understood current ecologies (let alone their ecological histories). To understand the relationship between defined ecological challenges and trajectories of QS evolution, we used an agent-based simulation modeling approach. Given genetic mixing, our simulations produce behaviors that recapitulate features of diverse microbial QS systems, including coercive (high signal/low response) and generalized reciprocity (signal auto-regulation) strategists — that separately and in combination contribute to QS-dependent resilience of QS-controlled cooperation in the face of diverse cheats. We contrast our in silico results given defined ecological challenges with bacterial QS architectures that have evolved under largely unknown ecological contexts, highlighting the critical role of genetic constraints in shaping the shorter term (experimental evolution) dynamics of QS. More broadly, we see experimental evolution of digital organisms as a complementary tool in the search to understand the emergence of complex QS architectures and functions.
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spelling pubmed-72481192020-06-04 In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies Wang, Yifei Rattray, Jennifer B. Thomas, Stephen A. Gurney, James Brown, Sam P. Sci Rep Article Many species of bacteria collectively sense and respond to their social and physical environment via ‘quorum sensing’ (QS), a communication system controlling extracellular cooperative traits. Despite detailed understanding of the mechanisms of signal production and response, there remains considerable debate over the functional role(s) of QS: in short, what is it for? Experimental studies have found support for diverse functional roles: density sensing, mass-transfer sensing, genotype sensing, etc. While consistent with theory, these results cannot separate whether these functions were drivers of QS adaption, or simply artifacts or ‘spandrels’ of systems shaped by distinct ecological pressures. The challenge of separating spandrels from drivers of adaptation is particularly hard to address using extant bacterial species with poorly understood current ecologies (let alone their ecological histories). To understand the relationship between defined ecological challenges and trajectories of QS evolution, we used an agent-based simulation modeling approach. Given genetic mixing, our simulations produce behaviors that recapitulate features of diverse microbial QS systems, including coercive (high signal/low response) and generalized reciprocity (signal auto-regulation) strategists — that separately and in combination contribute to QS-dependent resilience of QS-controlled cooperation in the face of diverse cheats. We contrast our in silico results given defined ecological challenges with bacterial QS architectures that have evolved under largely unknown ecological contexts, highlighting the critical role of genetic constraints in shaping the shorter term (experimental evolution) dynamics of QS. More broadly, we see experimental evolution of digital organisms as a complementary tool in the search to understand the emergence of complex QS architectures and functions. Nature Publishing Group UK 2020-05-25 /pmc/articles/PMC7248119/ /pubmed/32451396 http://dx.doi.org/10.1038/s41598-020-65076-z Text en © The Author(s) 2020 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
Wang, Yifei
Rattray, Jennifer B.
Thomas, Stephen A.
Gurney, James
Brown, Sam P.
In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies
title In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies
title_full In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies
title_fullStr In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies
title_full_unstemmed In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies
title_short In silico bacteria evolve robust cooperaion via complex quorum-sensing strategies
title_sort in silico bacteria evolve robust cooperaion via complex quorum-sensing strategies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248119/
https://www.ncbi.nlm.nih.gov/pubmed/32451396
http://dx.doi.org/10.1038/s41598-020-65076-z
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