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Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish

BACKGROUND: Marine holobionts depend on microbial members for health and nutrient cycling. This is particularly evident in cnidarian-algae symbioses that facilitate energy and nutrient acquisition. However, this partnership is highly sensitive to environmental change—including eutrophication—that ca...

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Autores principales: Röthig, Till, Puntin, Giulia, Wong, Jane C. Y., Burian, Alfred, McLeod, Wendy, Baker, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173792/
https://www.ncbi.nlm.nih.gov/pubmed/34078452
http://dx.doi.org/10.1186/s40168-021-01075-0
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author Röthig, Till
Puntin, Giulia
Wong, Jane C. Y.
Burian, Alfred
McLeod, Wendy
Baker, David M.
author_facet Röthig, Till
Puntin, Giulia
Wong, Jane C. Y.
Burian, Alfred
McLeod, Wendy
Baker, David M.
author_sort Röthig, Till
collection PubMed
description BACKGROUND: Marine holobionts depend on microbial members for health and nutrient cycling. This is particularly evident in cnidarian-algae symbioses that facilitate energy and nutrient acquisition. However, this partnership is highly sensitive to environmental change—including eutrophication—that causes dysbiosis and contributes to global coral reef decline. Yet, some holobionts exhibit resistance to dysbiosis in eutrophic environments, including the obligate photosymbiotic scyphomedusa Cassiopea xamachana. METHODS: Our aim was to assess the mechanisms in C. xamachana that stabilize symbiotic relationships. We combined labelled bicarbonate ((13)C) and nitrate ((15)N) with metabarcoding approaches to evaluate nutrient cycling and microbial community composition in symbiotic and aposymbiotic medusae. RESULTS: C-fixation and cycling by algal Symbiodiniaceae was essential for C. xamachana as even at high heterotrophic feeding rates aposymbiotic medusae continuously lost weight. Heterotrophically acquired C and N were readily shared among host and algae. This was in sharp contrast to nitrate assimilation by Symbiodiniaceae, which appeared to be strongly restricted. Instead, the bacterial microbiome seemed to play a major role in the holobiont’s DIN assimilation as uptake rates showed a significant positive relationship with phylogenetic diversity of medusa-associated bacteria. This is corroborated by inferred functional capacity that links the dominant bacterial taxa (~90 %) to nitrogen cycling. Observed bacterial community structure differed between apo- and symbiotic C. xamachana putatively highlighting enrichment of ammonium oxidizers and nitrite reducers and depletion of nitrogen-fixers in symbiotic medusae. CONCLUSION: Host, algal symbionts, and bacterial associates contribute to regulated nutrient assimilation and cycling in C. xamachana. We found that the bacterial microbiome of symbiotic medusae was seemingly structured to increase DIN removal and enforce algal N-limitation—a mechanism that would help to stabilize the host-algae relationship even under eutrophic conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01075-0.
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spelling pubmed-81737922021-06-03 Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish Röthig, Till Puntin, Giulia Wong, Jane C. Y. Burian, Alfred McLeod, Wendy Baker, David M. Microbiome Research BACKGROUND: Marine holobionts depend on microbial members for health and nutrient cycling. This is particularly evident in cnidarian-algae symbioses that facilitate energy and nutrient acquisition. However, this partnership is highly sensitive to environmental change—including eutrophication—that causes dysbiosis and contributes to global coral reef decline. Yet, some holobionts exhibit resistance to dysbiosis in eutrophic environments, including the obligate photosymbiotic scyphomedusa Cassiopea xamachana. METHODS: Our aim was to assess the mechanisms in C. xamachana that stabilize symbiotic relationships. We combined labelled bicarbonate ((13)C) and nitrate ((15)N) with metabarcoding approaches to evaluate nutrient cycling and microbial community composition in symbiotic and aposymbiotic medusae. RESULTS: C-fixation and cycling by algal Symbiodiniaceae was essential for C. xamachana as even at high heterotrophic feeding rates aposymbiotic medusae continuously lost weight. Heterotrophically acquired C and N were readily shared among host and algae. This was in sharp contrast to nitrate assimilation by Symbiodiniaceae, which appeared to be strongly restricted. Instead, the bacterial microbiome seemed to play a major role in the holobiont’s DIN assimilation as uptake rates showed a significant positive relationship with phylogenetic diversity of medusa-associated bacteria. This is corroborated by inferred functional capacity that links the dominant bacterial taxa (~90 %) to nitrogen cycling. Observed bacterial community structure differed between apo- and symbiotic C. xamachana putatively highlighting enrichment of ammonium oxidizers and nitrite reducers and depletion of nitrogen-fixers in symbiotic medusae. CONCLUSION: Host, algal symbionts, and bacterial associates contribute to regulated nutrient assimilation and cycling in C. xamachana. We found that the bacterial microbiome of symbiotic medusae was seemingly structured to increase DIN removal and enforce algal N-limitation—a mechanism that would help to stabilize the host-algae relationship even under eutrophic conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01075-0. BioMed Central 2021-06-02 /pmc/articles/PMC8173792/ /pubmed/34078452 http://dx.doi.org/10.1186/s40168-021-01075-0 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
Röthig, Till
Puntin, Giulia
Wong, Jane C. Y.
Burian, Alfred
McLeod, Wendy
Baker, David M.
Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish
title Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish
title_full Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish
title_fullStr Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish
title_full_unstemmed Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish
title_short Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish
title_sort holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173792/
https://www.ncbi.nlm.nih.gov/pubmed/34078452
http://dx.doi.org/10.1186/s40168-021-01075-0
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