Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kelsic, Eric D., Zhao, Jeffrey, Vetsigian, Kalin, Kishony, Roy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
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
_version_ 1782387570914623488
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
work_keys_str_mv AT kelsicericd counteractionofantibioticproductionanddegradationstabilizesmicrobialcommunities
AT zhaojeffrey counteractionofantibioticproductionanddegradationstabilizesmicrobialcommunities
AT vetsigiankalin counteractionofantibioticproductionanddegradationstabilizesmicrobialcommunities
AT kishonyroy counteractionofantibioticproductionanddegradationstabilizesmicrobialcommunities