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Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating
Much of our understanding of bacterial behavior stems from studies in liquid culture. In nature, however, bacteria frequently live in densely packed spatially-structured communities. How does spatial structure affect bacterial cooperative behaviors? In this work, we examine rhamnolipid production—a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821651/ https://www.ncbi.nlm.nih.gov/pubmed/35132084 http://dx.doi.org/10.1038/s41467-022-28321-9 |
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author | Monaco, Hilary Liu, Kevin S. Sereno, Tiago Deforet, Maxime Taylor, Bradford P. Chen, Yanyan Reagor, Caleb C. Xavier, Joao B. |
author_facet | Monaco, Hilary Liu, Kevin S. Sereno, Tiago Deforet, Maxime Taylor, Bradford P. Chen, Yanyan Reagor, Caleb C. Xavier, Joao B. |
author_sort | Monaco, Hilary |
collection | PubMed |
description | Much of our understanding of bacterial behavior stems from studies in liquid culture. In nature, however, bacteria frequently live in densely packed spatially-structured communities. How does spatial structure affect bacterial cooperative behaviors? In this work, we examine rhamnolipid production—a cooperative and virulent behavior of Pseudomonas aeruginosa. Here we show that, in striking contrast to well-mixed liquid culture, rhamnolipid gene expression in spatially-structured colonies is strongly associated with colony specific growth rate, and is impacted by perturbation with diffusible quorum signals. To interpret these findings, we construct a data-driven statistical inference model which captures a length-scale of bacterial interaction that develops over time. Finally, we find that perturbation of P. aeruginosa swarms with quorum signals preserves the cooperating genotype in competition, rather than creating opportunities for cheaters. Overall, our data demonstrate that the complex response to spatial localization is key to preserving bacterial cooperative behaviors. |
format | Online Article Text |
id | pubmed-8821651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88216512022-02-18 Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating Monaco, Hilary Liu, Kevin S. Sereno, Tiago Deforet, Maxime Taylor, Bradford P. Chen, Yanyan Reagor, Caleb C. Xavier, Joao B. Nat Commun Article Much of our understanding of bacterial behavior stems from studies in liquid culture. In nature, however, bacteria frequently live in densely packed spatially-structured communities. How does spatial structure affect bacterial cooperative behaviors? In this work, we examine rhamnolipid production—a cooperative and virulent behavior of Pseudomonas aeruginosa. Here we show that, in striking contrast to well-mixed liquid culture, rhamnolipid gene expression in spatially-structured colonies is strongly associated with colony specific growth rate, and is impacted by perturbation with diffusible quorum signals. To interpret these findings, we construct a data-driven statistical inference model which captures a length-scale of bacterial interaction that develops over time. Finally, we find that perturbation of P. aeruginosa swarms with quorum signals preserves the cooperating genotype in competition, rather than creating opportunities for cheaters. Overall, our data demonstrate that the complex response to spatial localization is key to preserving bacterial cooperative behaviors. Nature Publishing Group UK 2022-02-07 /pmc/articles/PMC8821651/ /pubmed/35132084 http://dx.doi.org/10.1038/s41467-022-28321-9 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 Monaco, Hilary Liu, Kevin S. Sereno, Tiago Deforet, Maxime Taylor, Bradford P. Chen, Yanyan Reagor, Caleb C. Xavier, Joao B. Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating |
title | Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating |
title_full | Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating |
title_fullStr | Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating |
title_full_unstemmed | Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating |
title_short | Spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating |
title_sort | spatial-temporal dynamics of a microbial cooperative behavior resistant to cheating |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821651/ https://www.ncbi.nlm.nih.gov/pubmed/35132084 http://dx.doi.org/10.1038/s41467-022-28321-9 |
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