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Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation
By nature of their small size, dense growth and frequent need for extracellular metabolism, microbes face persistent public goods dilemmas. Genetic assortment is the only general solution stabilizing cooperation, but all known mechanisms structuring microbial populations depend on the availability o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303878/ https://www.ncbi.nlm.nih.gov/pubmed/28165005 http://dx.doi.org/10.1038/ncomms14371 |
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author | McNally, Luke Bernardy, Eryn Thomas, Jacob Kalziqi, Arben Pentz, Jennifer Brown, Sam P. Hammer, Brian K. Yunker, Peter J. Ratcliff, William C. |
author_facet | McNally, Luke Bernardy, Eryn Thomas, Jacob Kalziqi, Arben Pentz, Jennifer Brown, Sam P. Hammer, Brian K. Yunker, Peter J. Ratcliff, William C. |
author_sort | McNally, Luke |
collection | PubMed |
description | By nature of their small size, dense growth and frequent need for extracellular metabolism, microbes face persistent public goods dilemmas. Genetic assortment is the only general solution stabilizing cooperation, but all known mechanisms structuring microbial populations depend on the availability of free space, an often unrealistic constraint. Here we describe a class of self-organization that operates within densely packed bacterial populations. Through mathematical modelling and experiments with Vibrio cholerae, we show how killing adjacent competitors via the Type VI secretion system (T6SS) precipitates phase separation via the ‘Model A' universality class of order-disorder transition mediated by killing. We mathematically demonstrate that T6SS-mediated killing should favour the evolution of public goods cooperation, and empirically support this prediction using a phylogenetic comparative analysis. This work illustrates the twin role played by the T6SS, dealing death to local competitors while simultaneously creating conditions potentially favouring the evolution of cooperation with kin. |
format | Online Article Text |
id | pubmed-5303878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53038782017-02-27 Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation McNally, Luke Bernardy, Eryn Thomas, Jacob Kalziqi, Arben Pentz, Jennifer Brown, Sam P. Hammer, Brian K. Yunker, Peter J. Ratcliff, William C. Nat Commun Article By nature of their small size, dense growth and frequent need for extracellular metabolism, microbes face persistent public goods dilemmas. Genetic assortment is the only general solution stabilizing cooperation, but all known mechanisms structuring microbial populations depend on the availability of free space, an often unrealistic constraint. Here we describe a class of self-organization that operates within densely packed bacterial populations. Through mathematical modelling and experiments with Vibrio cholerae, we show how killing adjacent competitors via the Type VI secretion system (T6SS) precipitates phase separation via the ‘Model A' universality class of order-disorder transition mediated by killing. We mathematically demonstrate that T6SS-mediated killing should favour the evolution of public goods cooperation, and empirically support this prediction using a phylogenetic comparative analysis. This work illustrates the twin role played by the T6SS, dealing death to local competitors while simultaneously creating conditions potentially favouring the evolution of cooperation with kin. Nature Publishing Group 2017-02-06 /pmc/articles/PMC5303878/ /pubmed/28165005 http://dx.doi.org/10.1038/ncomms14371 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article McNally, Luke Bernardy, Eryn Thomas, Jacob Kalziqi, Arben Pentz, Jennifer Brown, Sam P. Hammer, Brian K. Yunker, Peter J. Ratcliff, William C. Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation |
title | Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation |
title_full | Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation |
title_fullStr | Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation |
title_full_unstemmed | Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation |
title_short | Killing by Type VI secretion drives genetic phase separation and correlates with increased cooperation |
title_sort | killing by type vi secretion drives genetic phase separation and correlates with increased cooperation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303878/ https://www.ncbi.nlm.nih.gov/pubmed/28165005 http://dx.doi.org/10.1038/ncomms14371 |
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