Cargando…
A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies
Southern Ocean (SO) diatoms play an important role in global carbon flux, and their influence on carbon export is directly linked to interactions with epiphytic bacteria. Bacterial symbionts that increase diatom growth promote atmospheric carbon uptake, while bacterial degraders divert diatom biomas...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723598/ https://www.ncbi.nlm.nih.gov/pubmed/37938401 http://dx.doi.org/10.1038/s43705-022-00181-w |
_version_ | 1784844218931347456 |
---|---|
author | Andrew, Sarah Wilson, Travis Smith, Stephanie Marchetti, Adrian Septer, Alecia N. |
author_facet | Andrew, Sarah Wilson, Travis Smith, Stephanie Marchetti, Adrian Septer, Alecia N. |
author_sort | Andrew, Sarah |
collection | PubMed |
description | Southern Ocean (SO) diatoms play an important role in global carbon flux, and their influence on carbon export is directly linked to interactions with epiphytic bacteria. Bacterial symbionts that increase diatom growth promote atmospheric carbon uptake, while bacterial degraders divert diatom biomass into the microbial loop where it can then be released as carbon dioxide through respiration. To further explore SO diatom-bacterial associations, a natural model system is needed that is representative of these diverse and important interactions. Here, we use concurrent cultivation to isolate a species of the ecologically-important SO diatom, Pseudo-nitzschia subcurvata, and its co-occurring bacteria. Although vitamin-depleted, axenic Pseudo-nitzschia grew poorly in culture, addition of a co-isolated Roseobacter promoted diatom growth, while addition of a co-isolated Flavobacterium negatively impacted diatom growth. Microscopy revealed both bacterial isolates are physically associated with diatom cells and genome sequencing identified important predicted functions including vitamin synthesis, motility, cell attachment mechanisms, and diverse antimicrobial weapons that could be used for interbacterial competition. These findings revealed the natural coexistence of competing symbiotic strategies of diatom-associated bacteria in the SO, and the utility of this tripartite system, composed of a diatom and two bacterial strains, as a co-culture model to probe ecological-relevant interactions between diatoms and the bacteria that compete for access to the phycosphere. |
format | Online Article Text |
id | pubmed-9723598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97235982023-01-04 A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies Andrew, Sarah Wilson, Travis Smith, Stephanie Marchetti, Adrian Septer, Alecia N. ISME Commun Article Southern Ocean (SO) diatoms play an important role in global carbon flux, and their influence on carbon export is directly linked to interactions with epiphytic bacteria. Bacterial symbionts that increase diatom growth promote atmospheric carbon uptake, while bacterial degraders divert diatom biomass into the microbial loop where it can then be released as carbon dioxide through respiration. To further explore SO diatom-bacterial associations, a natural model system is needed that is representative of these diverse and important interactions. Here, we use concurrent cultivation to isolate a species of the ecologically-important SO diatom, Pseudo-nitzschia subcurvata, and its co-occurring bacteria. Although vitamin-depleted, axenic Pseudo-nitzschia grew poorly in culture, addition of a co-isolated Roseobacter promoted diatom growth, while addition of a co-isolated Flavobacterium negatively impacted diatom growth. Microscopy revealed both bacterial isolates are physically associated with diatom cells and genome sequencing identified important predicted functions including vitamin synthesis, motility, cell attachment mechanisms, and diverse antimicrobial weapons that could be used for interbacterial competition. These findings revealed the natural coexistence of competing symbiotic strategies of diatom-associated bacteria in the SO, and the utility of this tripartite system, composed of a diatom and two bacterial strains, as a co-culture model to probe ecological-relevant interactions between diatoms and the bacteria that compete for access to the phycosphere. Nature Publishing Group UK 2022-10-03 /pmc/articles/PMC9723598/ /pubmed/37938401 http://dx.doi.org/10.1038/s43705-022-00181-w 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 Andrew, Sarah Wilson, Travis Smith, Stephanie Marchetti, Adrian Septer, Alecia N. A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies |
title | A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies |
title_full | A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies |
title_fullStr | A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies |
title_full_unstemmed | A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies |
title_short | A tripartite model system for Southern Ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies |
title_sort | tripartite model system for southern ocean diatom-bacterial interactions reveals the coexistence of competing symbiotic strategies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723598/ https://www.ncbi.nlm.nih.gov/pubmed/37938401 http://dx.doi.org/10.1038/s43705-022-00181-w |
work_keys_str_mv | AT andrewsarah atripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT wilsontravis atripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT smithstephanie atripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT marchettiadrian atripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT septeralecian atripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT andrewsarah tripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT wilsontravis tripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT smithstephanie tripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT marchettiadrian tripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies AT septeralecian tripartitemodelsystemforsouthernoceandiatombacterialinteractionsrevealsthecoexistenceofcompetingsymbioticstrategies |