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Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability

Multi-step substrate consumption pathways can promote microbial biodiversity via cross-feeding. If one cell type preferentially consumes a primary substrate rather than the subsequently formed intermediates, then other cell types can specialize in consuming the intermediates. While this mechanism fo...

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Autores principales: Dolinšek, Jan, Ramoneda, Josep, Johnson, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723679/
https://www.ncbi.nlm.nih.gov/pubmed/37938324
http://dx.doi.org/10.1038/s43705-022-00160-1
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author Dolinšek, Jan
Ramoneda, Josep
Johnson, David R.
author_facet Dolinšek, Jan
Ramoneda, Josep
Johnson, David R.
author_sort Dolinšek, Jan
collection PubMed
description Multi-step substrate consumption pathways can promote microbial biodiversity via cross-feeding. If one cell type preferentially consumes a primary substrate rather than the subsequently formed intermediates, then other cell types can specialize in consuming the intermediates. While this mechanism for promoting biodiversity is established, predicting the long-term persistence of such cross-feeding interactions remains challenging. Under what conditions will the interaction (and thus biodiversity) persist or disappear? To address this question, we propagated co-cultures of two isogenic strains of the bacterium Pseudomonas stutzeri. One completely reduces nitrate to nitrogen gas but preferentially reduces nitrate rather than nitrite (referred to as the generalist), while the other only reduces nitrite to nitrogen gas (referred to as the specialist). We found that the two strains coexist via nitrite cross-feeding when grown together, but the initial ratio of specialist-to-generalist (r(S/G)) determines the long-term dynamics of the co-culture. Co-cultures with large initial r(S/G)s converge to the same r(S/G) and persist thereafter. Co-cultures with small initial r(S/G)s also converge to the same r(S/G) but then become increasingly dominated by the generalist. The likely cause of these different dynamics is that the initial r(S/G) determines the initial environment, which in turn determines the initial selection pressures and phenotypes acquired by the generalist. Our results demonstrate that initial community composition controls the long-term dynamics and persistence of a cross-feeding interaction, and is therefore an important factor for community development and for engineering communities to achieve desired outcomes.
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spelling pubmed-97236792023-01-04 Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability Dolinšek, Jan Ramoneda, Josep Johnson, David R. ISME Commun Article Multi-step substrate consumption pathways can promote microbial biodiversity via cross-feeding. If one cell type preferentially consumes a primary substrate rather than the subsequently formed intermediates, then other cell types can specialize in consuming the intermediates. While this mechanism for promoting biodiversity is established, predicting the long-term persistence of such cross-feeding interactions remains challenging. Under what conditions will the interaction (and thus biodiversity) persist or disappear? To address this question, we propagated co-cultures of two isogenic strains of the bacterium Pseudomonas stutzeri. One completely reduces nitrate to nitrogen gas but preferentially reduces nitrate rather than nitrite (referred to as the generalist), while the other only reduces nitrite to nitrogen gas (referred to as the specialist). We found that the two strains coexist via nitrite cross-feeding when grown together, but the initial ratio of specialist-to-generalist (r(S/G)) determines the long-term dynamics of the co-culture. Co-cultures with large initial r(S/G)s converge to the same r(S/G) and persist thereafter. Co-cultures with small initial r(S/G)s also converge to the same r(S/G) but then become increasingly dominated by the generalist. The likely cause of these different dynamics is that the initial r(S/G) determines the initial environment, which in turn determines the initial selection pressures and phenotypes acquired by the generalist. Our results demonstrate that initial community composition controls the long-term dynamics and persistence of a cross-feeding interaction, and is therefore an important factor for community development and for engineering communities to achieve desired outcomes. Nature Publishing Group UK 2022-08-24 /pmc/articles/PMC9723679/ /pubmed/37938324 http://dx.doi.org/10.1038/s43705-022-00160-1 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
Dolinšek, Jan
Ramoneda, Josep
Johnson, David R.
Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability
title Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability
title_full Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability
title_fullStr Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability
title_full_unstemmed Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability
title_short Initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability
title_sort initial community composition determines the long-term dynamics of a microbial cross-feeding interaction by modulating niche availability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723679/
https://www.ncbi.nlm.nih.gov/pubmed/37938324
http://dx.doi.org/10.1038/s43705-022-00160-1
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