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Historical contingencies and phage induction diversify bacterioplankton communities at the microscale

In many natural environments, microorganisms decompose microscale resource patches made of complex organic matter. The growth and collapse of populations on these resource patches unfold within spatial ranges of a few hundred micrometers or less, making such microscale ecosystems hotspots of heterot...

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Autores principales: Szabo, Rachel E., Pontrelli, Sammy, Grilli, Jacopo, Schwartzman, Julia A., Pollak, Shaul, Sauer, Uwe, Cordero, Otto X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335236/
https://www.ncbi.nlm.nih.gov/pubmed/35862452
http://dx.doi.org/10.1073/pnas.2117748119
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author Szabo, Rachel E.
Pontrelli, Sammy
Grilli, Jacopo
Schwartzman, Julia A.
Pollak, Shaul
Sauer, Uwe
Cordero, Otto X.
author_facet Szabo, Rachel E.
Pontrelli, Sammy
Grilli, Jacopo
Schwartzman, Julia A.
Pollak, Shaul
Sauer, Uwe
Cordero, Otto X.
author_sort Szabo, Rachel E.
collection PubMed
description In many natural environments, microorganisms decompose microscale resource patches made of complex organic matter. The growth and collapse of populations on these resource patches unfold within spatial ranges of a few hundred micrometers or less, making such microscale ecosystems hotspots of heterotrophic metabolism. Despite the potential importance of patch-level dynamics for the large-scale functioning of heterotrophic microbial communities, we have not yet been able to delineate the ecological processes that control natural populations at the microscale. Here, we address this challenge by characterizing the natural marine communities that assembled on over 1,000 individual microscale particles of chitin, the most abundant marine polysaccharide. Using low-template shotgun metagenomics and imaging, we find significant variation in microscale community composition despite the similarity in initial species pools across replicates. Chitin-degrading taxa that were rare in seawater established large populations on a subset of particles, resulting in a wide range of predicted chitinolytic abilities and biomass at the level of individual particles. We show, through a mathematical model, that this variability can be attributed to stochastic colonization and historical contingencies affecting the tempo of growth on particles. We find evidence that one biological process leading to such noisy growth across particles is differential predation by temperate bacteriophages of chitin-degrading strains, the keystone members of the community. Thus, initial stochasticity in assembly states on individual particles, amplified through ecological interactions, may have significant consequences for the diversity and functionality of systems of microscale patches.
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spelling pubmed-93352362022-07-30 Historical contingencies and phage induction diversify bacterioplankton communities at the microscale Szabo, Rachel E. Pontrelli, Sammy Grilli, Jacopo Schwartzman, Julia A. Pollak, Shaul Sauer, Uwe Cordero, Otto X. Proc Natl Acad Sci U S A Biological Sciences In many natural environments, microorganisms decompose microscale resource patches made of complex organic matter. The growth and collapse of populations on these resource patches unfold within spatial ranges of a few hundred micrometers or less, making such microscale ecosystems hotspots of heterotrophic metabolism. Despite the potential importance of patch-level dynamics for the large-scale functioning of heterotrophic microbial communities, we have not yet been able to delineate the ecological processes that control natural populations at the microscale. Here, we address this challenge by characterizing the natural marine communities that assembled on over 1,000 individual microscale particles of chitin, the most abundant marine polysaccharide. Using low-template shotgun metagenomics and imaging, we find significant variation in microscale community composition despite the similarity in initial species pools across replicates. Chitin-degrading taxa that were rare in seawater established large populations on a subset of particles, resulting in a wide range of predicted chitinolytic abilities and biomass at the level of individual particles. We show, through a mathematical model, that this variability can be attributed to stochastic colonization and historical contingencies affecting the tempo of growth on particles. We find evidence that one biological process leading to such noisy growth across particles is differential predation by temperate bacteriophages of chitin-degrading strains, the keystone members of the community. Thus, initial stochasticity in assembly states on individual particles, amplified through ecological interactions, may have significant consequences for the diversity and functionality of systems of microscale patches. National Academy of Sciences 2022-07-21 2022-07-26 /pmc/articles/PMC9335236/ /pubmed/35862452 http://dx.doi.org/10.1073/pnas.2117748119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Szabo, Rachel E.
Pontrelli, Sammy
Grilli, Jacopo
Schwartzman, Julia A.
Pollak, Shaul
Sauer, Uwe
Cordero, Otto X.
Historical contingencies and phage induction diversify bacterioplankton communities at the microscale
title Historical contingencies and phage induction diversify bacterioplankton communities at the microscale
title_full Historical contingencies and phage induction diversify bacterioplankton communities at the microscale
title_fullStr Historical contingencies and phage induction diversify bacterioplankton communities at the microscale
title_full_unstemmed Historical contingencies and phage induction diversify bacterioplankton communities at the microscale
title_short Historical contingencies and phage induction diversify bacterioplankton communities at the microscale
title_sort historical contingencies and phage induction diversify bacterioplankton communities at the microscale
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335236/
https://www.ncbi.nlm.nih.gov/pubmed/35862452
http://dx.doi.org/10.1073/pnas.2117748119
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