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Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum
Bacterial remineralization of algal organic matter fuels algal growth but is rarely quantified. Consequently, we cannot currently predict whether some bacterial taxa may provide more remineralized nutrients to algae than others. Here, we quantified bacterial incorporation of algal-derived complex di...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499878/ https://www.ncbi.nlm.nih.gov/pubmed/37704622 http://dx.doi.org/10.1038/s41467-023-41179-9 |
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author | Mayali, Xavier Samo, Ty J. Kimbrel, Jeff A. Morris, Megan M. Rolison, Kristina Swink, Courtney Ramon, Christina Kim, Young-Mo Munoz-Munoz, Nathalie Nicora, Carrie Purvine, Sam Lipton, Mary Stuart, Rhona K. Weber, Peter K. |
author_facet | Mayali, Xavier Samo, Ty J. Kimbrel, Jeff A. Morris, Megan M. Rolison, Kristina Swink, Courtney Ramon, Christina Kim, Young-Mo Munoz-Munoz, Nathalie Nicora, Carrie Purvine, Sam Lipton, Mary Stuart, Rhona K. Weber, Peter K. |
author_sort | Mayali, Xavier |
collection | PubMed |
description | Bacterial remineralization of algal organic matter fuels algal growth but is rarely quantified. Consequently, we cannot currently predict whether some bacterial taxa may provide more remineralized nutrients to algae than others. Here, we quantified bacterial incorporation of algal-derived complex dissolved organic carbon and nitrogen and algal incorporation of remineralized carbon and nitrogen in fifteen bacterial co-cultures growing with the diatom Phaeodactylum tricornutum at the single-cell level using isotope tracing and nanoSIMS. We found unexpected strain-to-strain and cell-to-cell variability in net carbon and nitrogen incorporation, including non-ubiquitous complex organic nitrogen utilization and remineralization. We used these data to identify three distinct functional guilds of metabolic interactions, which we termed macromolecule remineralizers, macromolecule users, and small-molecule users, the latter exhibiting efficient growth under low carbon availability. The functional guilds were not linked to phylogeny and could not be elucidated strictly from metabolic capacity as predicted by comparative genomics, highlighting the need for direct activity-based measurements in ecological studies of microbial metabolic interactions. |
format | Online Article Text |
id | pubmed-10499878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104998782023-09-15 Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum Mayali, Xavier Samo, Ty J. Kimbrel, Jeff A. Morris, Megan M. Rolison, Kristina Swink, Courtney Ramon, Christina Kim, Young-Mo Munoz-Munoz, Nathalie Nicora, Carrie Purvine, Sam Lipton, Mary Stuart, Rhona K. Weber, Peter K. Nat Commun Article Bacterial remineralization of algal organic matter fuels algal growth but is rarely quantified. Consequently, we cannot currently predict whether some bacterial taxa may provide more remineralized nutrients to algae than others. Here, we quantified bacterial incorporation of algal-derived complex dissolved organic carbon and nitrogen and algal incorporation of remineralized carbon and nitrogen in fifteen bacterial co-cultures growing with the diatom Phaeodactylum tricornutum at the single-cell level using isotope tracing and nanoSIMS. We found unexpected strain-to-strain and cell-to-cell variability in net carbon and nitrogen incorporation, including non-ubiquitous complex organic nitrogen utilization and remineralization. We used these data to identify three distinct functional guilds of metabolic interactions, which we termed macromolecule remineralizers, macromolecule users, and small-molecule users, the latter exhibiting efficient growth under low carbon availability. The functional guilds were not linked to phylogeny and could not be elucidated strictly from metabolic capacity as predicted by comparative genomics, highlighting the need for direct activity-based measurements in ecological studies of microbial metabolic interactions. Nature Publishing Group UK 2023-09-13 /pmc/articles/PMC10499878/ /pubmed/37704622 http://dx.doi.org/10.1038/s41467-023-41179-9 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mayali, Xavier Samo, Ty J. Kimbrel, Jeff A. Morris, Megan M. Rolison, Kristina Swink, Courtney Ramon, Christina Kim, Young-Mo Munoz-Munoz, Nathalie Nicora, Carrie Purvine, Sam Lipton, Mary Stuart, Rhona K. Weber, Peter K. Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum |
title | Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum |
title_full | Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum |
title_fullStr | Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum |
title_full_unstemmed | Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum |
title_short | Single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom Phaeodactylum tricornutum |
title_sort | single-cell isotope tracing reveals functional guilds of bacteria associated with the diatom phaeodactylum tricornutum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499878/ https://www.ncbi.nlm.nih.gov/pubmed/37704622 http://dx.doi.org/10.1038/s41467-023-41179-9 |
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