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Ecological drivers of bacterial community assembly in synthetic phycospheres
In the nutrient-rich region surrounding marine phytoplankton cells, heterotrophic bacterioplankton transform a major fraction of recently fixed carbon through the uptake and catabolism of phytoplankton metabolites. We sought to understand the rules by which marine bacterial communities assemble in t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035482/ https://www.ncbi.nlm.nih.gov/pubmed/32015111 http://dx.doi.org/10.1073/pnas.1917265117 |
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author | Fu, He Uchimiya, Mario Gore, Jeff Moran, Mary Ann |
author_facet | Fu, He Uchimiya, Mario Gore, Jeff Moran, Mary Ann |
author_sort | Fu, He |
collection | PubMed |
description | In the nutrient-rich region surrounding marine phytoplankton cells, heterotrophic bacterioplankton transform a major fraction of recently fixed carbon through the uptake and catabolism of phytoplankton metabolites. We sought to understand the rules by which marine bacterial communities assemble in these nutrient-enhanced phycospheres, specifically addressing the role of host resources in driving community coalescence. Synthetic systems with varying combinations of known exometabolites of marine phytoplankton were inoculated with seawater bacterial assemblages, and communities were transferred daily to mimic the average duration of natural phycospheres. We found that bacterial community assembly was predictable from linear combinations of the taxa maintained on each individual metabolite in the mixture, weighted for the growth each supported. Deviations from this simple additive resource model were observed but also attributed to resource-based factors via enhanced bacterial growth when host metabolites were available concurrently. The ability of photosynthetic hosts to shape bacterial associates through excreted metabolites represents a mechanism by which microbiomes with beneficial effects on host growth could be recruited. In the surface ocean, resource-based assembly of host-associated communities may underpin the evolution and maintenance of microbial interactions and determine the fate of a substantial portion of Earth’s primary production. |
format | Online Article Text |
id | pubmed-7035482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-70354822020-02-28 Ecological drivers of bacterial community assembly in synthetic phycospheres Fu, He Uchimiya, Mario Gore, Jeff Moran, Mary Ann Proc Natl Acad Sci U S A Biological Sciences In the nutrient-rich region surrounding marine phytoplankton cells, heterotrophic bacterioplankton transform a major fraction of recently fixed carbon through the uptake and catabolism of phytoplankton metabolites. We sought to understand the rules by which marine bacterial communities assemble in these nutrient-enhanced phycospheres, specifically addressing the role of host resources in driving community coalescence. Synthetic systems with varying combinations of known exometabolites of marine phytoplankton were inoculated with seawater bacterial assemblages, and communities were transferred daily to mimic the average duration of natural phycospheres. We found that bacterial community assembly was predictable from linear combinations of the taxa maintained on each individual metabolite in the mixture, weighted for the growth each supported. Deviations from this simple additive resource model were observed but also attributed to resource-based factors via enhanced bacterial growth when host metabolites were available concurrently. The ability of photosynthetic hosts to shape bacterial associates through excreted metabolites represents a mechanism by which microbiomes with beneficial effects on host growth could be recruited. In the surface ocean, resource-based assembly of host-associated communities may underpin the evolution and maintenance of microbial interactions and determine the fate of a substantial portion of Earth’s primary production. National Academy of Sciences 2020-02-18 2020-02-03 /pmc/articles/PMC7035482/ /pubmed/32015111 http://dx.doi.org/10.1073/pnas.1917265117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ 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 Fu, He Uchimiya, Mario Gore, Jeff Moran, Mary Ann Ecological drivers of bacterial community assembly in synthetic phycospheres |
title | Ecological drivers of bacterial community assembly in synthetic phycospheres |
title_full | Ecological drivers of bacterial community assembly in synthetic phycospheres |
title_fullStr | Ecological drivers of bacterial community assembly in synthetic phycospheres |
title_full_unstemmed | Ecological drivers of bacterial community assembly in synthetic phycospheres |
title_short | Ecological drivers of bacterial community assembly in synthetic phycospheres |
title_sort | ecological drivers of bacterial community assembly in synthetic phycospheres |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035482/ https://www.ncbi.nlm.nih.gov/pubmed/32015111 http://dx.doi.org/10.1073/pnas.1917265117 |
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