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Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible
With each cell division, phytoplankton create new space for primary colonization by marine bacteria. Although this surface microenvironment is available to all planktonic bacterial colonizers, we show the assembly of bacterial consortia on a cosmopolitan marine diatom to be highly specific and repro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242391/ https://www.ncbi.nlm.nih.gov/pubmed/32203123 http://dx.doi.org/10.1038/s41396-020-0631-5 |
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author | Mönnich, Julian Tebben, Jan Bergemann, Jennifer Case, Rebecca Wohlrab, Sylke Harder, Tilmann |
author_facet | Mönnich, Julian Tebben, Jan Bergemann, Jennifer Case, Rebecca Wohlrab, Sylke Harder, Tilmann |
author_sort | Mönnich, Julian |
collection | PubMed |
description | With each cell division, phytoplankton create new space for primary colonization by marine bacteria. Although this surface microenvironment is available to all planktonic bacterial colonizers, we show the assembly of bacterial consortia on a cosmopolitan marine diatom to be highly specific and reproducible. While phytoplankton–bacteria interactions play fundamental roles in marine ecosystems, namely primary production and the carbon cycle, the ecological paradigm behind epiphytic microbiome assembly remains poorly understood. In a replicated and repeated primary colonization experiment, we exposed the axenic diatom Thalassiosira rotula to several complex and compositionally different bacterial inocula derived from phytoplankton species of varying degrees of relatedness to the axenic Thalassiosira host or natural seawater. This revealed a convergent assembly of diverse and compositionally different bacterial inocula, containing up to 2071 operational taxonomic units (OTUs), towards a stable and reproducible core community. Four of these OTUs already accounted for a cumulative abundance of 60%. This core community was dominated by Rhodobacteraceae (30.5%), Alteromonadaceae (27.7%), and Oceanospirillales (18.5%) which was qualitatively and quantitatively most similar to its conspecific original. These findings reject a lottery assembly model of bacterial colonization and suggest selective microhabitat filtering. This is likely due to diatom host traits such as surface properties and different levels of specialization resulting in reciprocal stable-state associations. |
format | Online Article Text |
id | pubmed-7242391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72423912020-05-29 Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible Mönnich, Julian Tebben, Jan Bergemann, Jennifer Case, Rebecca Wohlrab, Sylke Harder, Tilmann ISME J Article With each cell division, phytoplankton create new space for primary colonization by marine bacteria. Although this surface microenvironment is available to all planktonic bacterial colonizers, we show the assembly of bacterial consortia on a cosmopolitan marine diatom to be highly specific and reproducible. While phytoplankton–bacteria interactions play fundamental roles in marine ecosystems, namely primary production and the carbon cycle, the ecological paradigm behind epiphytic microbiome assembly remains poorly understood. In a replicated and repeated primary colonization experiment, we exposed the axenic diatom Thalassiosira rotula to several complex and compositionally different bacterial inocula derived from phytoplankton species of varying degrees of relatedness to the axenic Thalassiosira host or natural seawater. This revealed a convergent assembly of diverse and compositionally different bacterial inocula, containing up to 2071 operational taxonomic units (OTUs), towards a stable and reproducible core community. Four of these OTUs already accounted for a cumulative abundance of 60%. This core community was dominated by Rhodobacteraceae (30.5%), Alteromonadaceae (27.7%), and Oceanospirillales (18.5%) which was qualitatively and quantitatively most similar to its conspecific original. These findings reject a lottery assembly model of bacterial colonization and suggest selective microhabitat filtering. This is likely due to diatom host traits such as surface properties and different levels of specialization resulting in reciprocal stable-state associations. Nature Publishing Group UK 2020-03-23 2020-06 /pmc/articles/PMC7242391/ /pubmed/32203123 http://dx.doi.org/10.1038/s41396-020-0631-5 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Mönnich, Julian Tebben, Jan Bergemann, Jennifer Case, Rebecca Wohlrab, Sylke Harder, Tilmann Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible |
title | Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible |
title_full | Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible |
title_fullStr | Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible |
title_full_unstemmed | Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible |
title_short | Niche-based assembly of bacterial consortia on the diatom Thalassiosira rotula is stable and reproducible |
title_sort | niche-based assembly of bacterial consortia on the diatom thalassiosira rotula is stable and reproducible |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242391/ https://www.ncbi.nlm.nih.gov/pubmed/32203123 http://dx.doi.org/10.1038/s41396-020-0631-5 |
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