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Counteraction of antibiotic production and degradation stabilizes microbial communities
A major challenge in theoretical ecology is understanding how natural microbial communities support species diversity(1-8), and in particular how antibiotic producing, sensitive and resistant species coexist(9-15). While cyclic “rock-paper-scissors” interactions can stabilize communities in spatial...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551410/ https://www.ncbi.nlm.nih.gov/pubmed/25992546 http://dx.doi.org/10.1038/nature14485 |
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author | Kelsic, Eric D. Zhao, Jeffrey Vetsigian, Kalin Kishony, Roy |
author_facet | Kelsic, Eric D. Zhao, Jeffrey Vetsigian, Kalin Kishony, Roy |
author_sort | Kelsic, Eric D. |
collection | PubMed |
description | A major challenge in theoretical ecology is understanding how natural microbial communities support species diversity(1-8), and in particular how antibiotic producing, sensitive and resistant species coexist(9-15). While cyclic “rock-paper-scissors” interactions can stabilize communities in spatial environments(9-11), coexistence in unstructured environments remains an enigma(12,16). Here, using simulations and analytical models, we show that the opposing actions of antibiotic production and degradation enable coexistence even in well-mixed environments. Coexistence depends on 3-way interactions where an antibiotic degrading species attenuates the inhibitory interactions between two other species. These 3-way interactions enable coexistence that is robust to substantial differences in inherent species growth rates and to invasion by “cheating” species that cease producing or degrading antibiotics. At least two antibiotics are required for stability, with greater numbers of antibiotics enabling more complex communities and diverse dynamical behaviors ranging from stable fixed-points to limit cycles and chaos. Together, these results show how multi-species antibiotic interactions can generate ecological stability in both spatial and mixed microbial communities, suggesting strategies for engineering synthetic ecosystems and highlighting the importance of toxin production and degradation for microbial biodiversity. |
format | Online Article Text |
id | pubmed-4551410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-45514102015-11-28 Counteraction of antibiotic production and degradation stabilizes microbial communities Kelsic, Eric D. Zhao, Jeffrey Vetsigian, Kalin Kishony, Roy Nature Article A major challenge in theoretical ecology is understanding how natural microbial communities support species diversity(1-8), and in particular how antibiotic producing, sensitive and resistant species coexist(9-15). While cyclic “rock-paper-scissors” interactions can stabilize communities in spatial environments(9-11), coexistence in unstructured environments remains an enigma(12,16). Here, using simulations and analytical models, we show that the opposing actions of antibiotic production and degradation enable coexistence even in well-mixed environments. Coexistence depends on 3-way interactions where an antibiotic degrading species attenuates the inhibitory interactions between two other species. These 3-way interactions enable coexistence that is robust to substantial differences in inherent species growth rates and to invasion by “cheating” species that cease producing or degrading antibiotics. At least two antibiotics are required for stability, with greater numbers of antibiotics enabling more complex communities and diverse dynamical behaviors ranging from stable fixed-points to limit cycles and chaos. Together, these results show how multi-species antibiotic interactions can generate ecological stability in both spatial and mixed microbial communities, suggesting strategies for engineering synthetic ecosystems and highlighting the importance of toxin production and degradation for microbial biodiversity. 2015-05-28 /pmc/articles/PMC4551410/ /pubmed/25992546 http://dx.doi.org/10.1038/nature14485 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Kelsic, Eric D. Zhao, Jeffrey Vetsigian, Kalin Kishony, Roy Counteraction of antibiotic production and degradation stabilizes microbial communities |
title | Counteraction of antibiotic production and degradation stabilizes microbial communities |
title_full | Counteraction of antibiotic production and degradation stabilizes microbial communities |
title_fullStr | Counteraction of antibiotic production and degradation stabilizes microbial communities |
title_full_unstemmed | Counteraction of antibiotic production and degradation stabilizes microbial communities |
title_short | Counteraction of antibiotic production and degradation stabilizes microbial communities |
title_sort | counteraction of antibiotic production and degradation stabilizes microbial communities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551410/ https://www.ncbi.nlm.nih.gov/pubmed/25992546 http://dx.doi.org/10.1038/nature14485 |
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