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Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana
BACKGROUND: Coral reefs are among the most diverse and productive ecosystems on Earth. This success relies on the coral’s association with a wide range of microorganisms, including dinoflagellates of the family Symbiodiniaceae that provide coral hosts with most of their organic carbon requirements....
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140459/ https://www.ncbi.nlm.nih.gov/pubmed/34020587 http://dx.doi.org/10.1186/s12866-021-02211-4 |
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author | Maire, Justin Blackall, Linda L. van Oppen, Madeleine J. H. |
author_facet | Maire, Justin Blackall, Linda L. van Oppen, Madeleine J. H. |
author_sort | Maire, Justin |
collection | PubMed |
description | BACKGROUND: Coral reefs are among the most diverse and productive ecosystems on Earth. This success relies on the coral’s association with a wide range of microorganisms, including dinoflagellates of the family Symbiodiniaceae that provide coral hosts with most of their organic carbon requirements. While bacterial associates have long been overlooked, research on these microorganisms is gaining traction, and deciphering bacterial identity and function is greatly enhancing our understanding of cnidarian biology. Here, we investigated bacterial communities in defensive tissues (acontia) of the coral model, the sea anemone Exaiptasia diaphana. Acontia are internal filaments that are ejected upon detection of an external threat and release toxins to repel predators. RESULTS: Using culturing techniques and 16S rRNA gene metabarcoding we identified bacterial communities associated with acontia of four Great Barrier Reef-sourced E. diaphana genotypes. We show that bacterial communities are similar across genotypes, and dominated by Alteromonadaceae, Vibrionaceae, Rhodobacteraceae, and Saprospiraceae. By analyzing abundant amplicon sequence variants (ASVs) from metabarcoding data from acontia and comparing these to data from whole anemones, we identified five potentially important bacterial genera of the acontia microbiome: Vibrio, Sulfitobacter, Marivita, Alteromonas, and Lewinella. The role of these bacteria within the acontia remains uninvestigated but could entail assistance in defense processes such as toxin production. CONCLUSIONS: This study provides insight into potential bacterial involvement in cnidarian defense tissues and highlights the need to study bacterial communities in individual compartments within a holobiont. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02211-4. |
format | Online Article Text |
id | pubmed-8140459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81404592021-05-25 Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana Maire, Justin Blackall, Linda L. van Oppen, Madeleine J. H. BMC Microbiol Research BACKGROUND: Coral reefs are among the most diverse and productive ecosystems on Earth. This success relies on the coral’s association with a wide range of microorganisms, including dinoflagellates of the family Symbiodiniaceae that provide coral hosts with most of their organic carbon requirements. While bacterial associates have long been overlooked, research on these microorganisms is gaining traction, and deciphering bacterial identity and function is greatly enhancing our understanding of cnidarian biology. Here, we investigated bacterial communities in defensive tissues (acontia) of the coral model, the sea anemone Exaiptasia diaphana. Acontia are internal filaments that are ejected upon detection of an external threat and release toxins to repel predators. RESULTS: Using culturing techniques and 16S rRNA gene metabarcoding we identified bacterial communities associated with acontia of four Great Barrier Reef-sourced E. diaphana genotypes. We show that bacterial communities are similar across genotypes, and dominated by Alteromonadaceae, Vibrionaceae, Rhodobacteraceae, and Saprospiraceae. By analyzing abundant amplicon sequence variants (ASVs) from metabarcoding data from acontia and comparing these to data from whole anemones, we identified five potentially important bacterial genera of the acontia microbiome: Vibrio, Sulfitobacter, Marivita, Alteromonas, and Lewinella. The role of these bacteria within the acontia remains uninvestigated but could entail assistance in defense processes such as toxin production. CONCLUSIONS: This study provides insight into potential bacterial involvement in cnidarian defense tissues and highlights the need to study bacterial communities in individual compartments within a holobiont. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02211-4. BioMed Central 2021-05-21 /pmc/articles/PMC8140459/ /pubmed/34020587 http://dx.doi.org/10.1186/s12866-021-02211-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Maire, Justin Blackall, Linda L. van Oppen, Madeleine J. H. Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana |
title | Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana |
title_full | Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana |
title_fullStr | Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana |
title_full_unstemmed | Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana |
title_short | Microbiome characterization of defensive tissues in the model anemone Exaiptasia diaphana |
title_sort | microbiome characterization of defensive tissues in the model anemone exaiptasia diaphana |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140459/ https://www.ncbi.nlm.nih.gov/pubmed/34020587 http://dx.doi.org/10.1186/s12866-021-02211-4 |
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