Phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture

Abstract The fundamental question of whether different microbial species will co-exist or compete in a given environment depends on context, composition and environmental constraints. Model microbial systems can yield some general principles related to this question. In this study we employed a natu...

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Autores principales: Nymul Khan, Yukari Maezato, Ryan S. McClure, Colin J. Brislawn, Jennifer M. Mobberley, Nancy Isern, William B. Chrisler, Lye Meng Markillie, Brett M. Barney, Hyun-Seob Song, William C. Nelson, Hans C. Bernstein
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/c7f655fb6f8f41f3a20d2783e62fb91e
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spelling oai:doaj.org-article:c7f655fb6f8f41f3a20d2783e62fb91e2021-12-02T15:08:49ZPhenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture10.1038/s41598-017-18630-12045-2322https://doaj.org/article/c7f655fb6f8f41f3a20d2783e62fb91e2018-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-18630-1https://doaj.org/toc/2045-2322Abstract The fundamental question of whether different microbial species will co-exist or compete in a given environment depends on context, composition and environmental constraints. Model microbial systems can yield some general principles related to this question. In this study we employed a naturally occurring co-culture composed of heterotrophic bacteria, Halomonas sp. HL-48 and Marinobacter sp. HL-58, to ask two fundamental scientific questions: 1) how do the phenotypes of two naturally co-existing species respond to partnership as compared to axenic growth? and 2) how do growth and molecular phenotypes of these species change with respect to competitive and commensal interactions? We hypothesized – and confirmed – that co-cultivation under glucose as the sole carbon source would result in competitive interactions. Similarly, when glucose was swapped with xylose, the interactions became commensal because Marinobacter HL-58 was supported by metabolites derived from Halomonas HL-48. Each species responded to partnership by changing both its growth and molecular phenotype as assayed via batch growth kinetics and global transcriptomics. These phenotypic responses depended on nutrient availability and so the environment ultimately controlled how they responded to each other. This simplified model community revealed that microbial interactions are context-specific and different environmental conditions dictate how interspecies partnerships will unfold.Nymul KhanYukari MaezatoRyan S. McClureColin J. BrislawnJennifer M. MobberleyNancy IsernWilliam B. ChrislerLye Meng MarkillieBrett M. BarneyHyun-Seob SongWilliam C. NelsonHans C. BernsteinNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Nymul Khan
Yukari Maezato
Ryan S. McClure
Colin J. Brislawn
Jennifer M. Mobberley
Nancy Isern
William B. Chrisler
Lye Meng Markillie
Brett M. Barney
Hyun-Seob Song
William C. Nelson
Hans C. Bernstein
Phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture
description Abstract The fundamental question of whether different microbial species will co-exist or compete in a given environment depends on context, composition and environmental constraints. Model microbial systems can yield some general principles related to this question. In this study we employed a naturally occurring co-culture composed of heterotrophic bacteria, Halomonas sp. HL-48 and Marinobacter sp. HL-58, to ask two fundamental scientific questions: 1) how do the phenotypes of two naturally co-existing species respond to partnership as compared to axenic growth? and 2) how do growth and molecular phenotypes of these species change with respect to competitive and commensal interactions? We hypothesized – and confirmed – that co-cultivation under glucose as the sole carbon source would result in competitive interactions. Similarly, when glucose was swapped with xylose, the interactions became commensal because Marinobacter HL-58 was supported by metabolites derived from Halomonas HL-48. Each species responded to partnership by changing both its growth and molecular phenotype as assayed via batch growth kinetics and global transcriptomics. These phenotypic responses depended on nutrient availability and so the environment ultimately controlled how they responded to each other. This simplified model community revealed that microbial interactions are context-specific and different environmental conditions dictate how interspecies partnerships will unfold.
format article
author Nymul Khan
Yukari Maezato
Ryan S. McClure
Colin J. Brislawn
Jennifer M. Mobberley
Nancy Isern
William B. Chrisler
Lye Meng Markillie
Brett M. Barney
Hyun-Seob Song
William C. Nelson
Hans C. Bernstein
author_facet Nymul Khan
Yukari Maezato
Ryan S. McClure
Colin J. Brislawn
Jennifer M. Mobberley
Nancy Isern
William B. Chrisler
Lye Meng Markillie
Brett M. Barney
Hyun-Seob Song
William C. Nelson
Hans C. Bernstein
author_sort Nymul Khan
title Phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture
title_short Phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture
title_full Phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture
title_fullStr Phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture
title_full_unstemmed Phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture
title_sort phenotypic responses to interspecies competition and commensalism in a naturally-derived microbial co-culture
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/c7f655fb6f8f41f3a20d2783e62fb91e
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