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Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community

Interactions among microbial community members can lead to emergent properties, such as enhanced productivity, stability, and robustness. Iron-oxide mats in acidic (pH 2–4), high-temperature (> 65 °C) springs of Yellowstone National Park contain relatively simple microbial communities and are wel...

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Autores principales: Hunt, Kristopher A., Jennings, Ryan M., Inskeep, William P., Carlson, Ross P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177205/
https://www.ncbi.nlm.nih.gov/pubmed/30260956
http://dx.doi.org/10.1371/journal.pcbi.1006431
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author Hunt, Kristopher A.
Jennings, Ryan M.
Inskeep, William P.
Carlson, Ross P.
author_facet Hunt, Kristopher A.
Jennings, Ryan M.
Inskeep, William P.
Carlson, Ross P.
author_sort Hunt, Kristopher A.
collection PubMed
description Interactions among microbial community members can lead to emergent properties, such as enhanced productivity, stability, and robustness. Iron-oxide mats in acidic (pH 2–4), high-temperature (> 65 °C) springs of Yellowstone National Park contain relatively simple microbial communities and are well-characterized geochemically. Consequently, these communities are excellent model systems for studying the metabolic activity of individual populations and key microbial interactions. The primary goals of the current study were to integrate data collected in situ with in silico calculations across process-scales encompassing enzymatic activity, cellular metabolism, community interactions, and ecosystem biogeochemistry, as well as to predict and quantify the functional limits of autotroph-heterotroph interactions. Metagenomic and transcriptomic data were used to reconstruct carbon and energy metabolisms of an important autotroph (Metallosphaera yellowstonensis) and heterotroph (Geoarchaeum sp. OSPB) from the studied Fe(III)-oxide mat communities. Standard and hybrid elementary flux mode and flux balance analyses of metabolic models predicted cellular- and community-level metabolic acclimations to simulated environmental stresses, respectively. In situ geochemical analyses, including oxygen depth-profiles, Fe(III)-oxide deposition rates, stable carbon isotopes and mat biomass concentrations, were combined with cellular models to explore autotroph-heterotroph interactions important to community structure-function. Integration of metabolic modeling with in situ measurements, including the relative population abundance of autotrophs to heterotrophs, demonstrated that Fe(III)-oxide mat communities operate at their maximum total community growth rate (i.e. sum of autotroph and heterotroph growth rates), as opposed to net community growth rate (i.e. total community growth rate subtracting autotroph consumed by heterotroph), as predicted from the maximum power principle. Integration of multiscale data with ecological theory provides a basis for predicting autotroph-heterotroph interactions and community-level cellular organization.
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spelling pubmed-61772052018-10-19 Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community Hunt, Kristopher A. Jennings, Ryan M. Inskeep, William P. Carlson, Ross P. PLoS Comput Biol Research Article Interactions among microbial community members can lead to emergent properties, such as enhanced productivity, stability, and robustness. Iron-oxide mats in acidic (pH 2–4), high-temperature (> 65 °C) springs of Yellowstone National Park contain relatively simple microbial communities and are well-characterized geochemically. Consequently, these communities are excellent model systems for studying the metabolic activity of individual populations and key microbial interactions. The primary goals of the current study were to integrate data collected in situ with in silico calculations across process-scales encompassing enzymatic activity, cellular metabolism, community interactions, and ecosystem biogeochemistry, as well as to predict and quantify the functional limits of autotroph-heterotroph interactions. Metagenomic and transcriptomic data were used to reconstruct carbon and energy metabolisms of an important autotroph (Metallosphaera yellowstonensis) and heterotroph (Geoarchaeum sp. OSPB) from the studied Fe(III)-oxide mat communities. Standard and hybrid elementary flux mode and flux balance analyses of metabolic models predicted cellular- and community-level metabolic acclimations to simulated environmental stresses, respectively. In situ geochemical analyses, including oxygen depth-profiles, Fe(III)-oxide deposition rates, stable carbon isotopes and mat biomass concentrations, were combined with cellular models to explore autotroph-heterotroph interactions important to community structure-function. Integration of metabolic modeling with in situ measurements, including the relative population abundance of autotrophs to heterotrophs, demonstrated that Fe(III)-oxide mat communities operate at their maximum total community growth rate (i.e. sum of autotroph and heterotroph growth rates), as opposed to net community growth rate (i.e. total community growth rate subtracting autotroph consumed by heterotroph), as predicted from the maximum power principle. Integration of multiscale data with ecological theory provides a basis for predicting autotroph-heterotroph interactions and community-level cellular organization. Public Library of Science 2018-09-27 /pmc/articles/PMC6177205/ /pubmed/30260956 http://dx.doi.org/10.1371/journal.pcbi.1006431 Text en © 2018 Hunt et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hunt, Kristopher A.
Jennings, Ryan M.
Inskeep, William P.
Carlson, Ross P.
Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community
title Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community
title_full Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community
title_fullStr Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community
title_full_unstemmed Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community
title_short Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community
title_sort multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177205/
https://www.ncbi.nlm.nih.gov/pubmed/30260956
http://dx.doi.org/10.1371/journal.pcbi.1006431
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