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Heat stress destabilizes symbiotic nutrient cycling in corals

Recurrent mass bleaching events are pushing coral reefs worldwide to the brink of ecological collapse. While the symptoms and consequences of this breakdown of the coral–algal symbiosis have been extensively characterized, our understanding of the underlying causes remains incomplete. Here, we inves...

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Autores principales: Rädecker, Nils, Pogoreutz, Claudia, Gegner, Hagen M., Cárdenas, Anny, Roth, Florian, Bougoure, Jeremy, Guagliardo, Paul, Wild, Christian, Pernice, Mathieu, Raina, Jean-Baptiste, Meibom, Anders, Voolstra, Christian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865147/
https://www.ncbi.nlm.nih.gov/pubmed/33500354
http://dx.doi.org/10.1073/pnas.2022653118
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author Rädecker, Nils
Pogoreutz, Claudia
Gegner, Hagen M.
Cárdenas, Anny
Roth, Florian
Bougoure, Jeremy
Guagliardo, Paul
Wild, Christian
Pernice, Mathieu
Raina, Jean-Baptiste
Meibom, Anders
Voolstra, Christian R.
author_facet Rädecker, Nils
Pogoreutz, Claudia
Gegner, Hagen M.
Cárdenas, Anny
Roth, Florian
Bougoure, Jeremy
Guagliardo, Paul
Wild, Christian
Pernice, Mathieu
Raina, Jean-Baptiste
Meibom, Anders
Voolstra, Christian R.
author_sort Rädecker, Nils
collection PubMed
description Recurrent mass bleaching events are pushing coral reefs worldwide to the brink of ecological collapse. While the symptoms and consequences of this breakdown of the coral–algal symbiosis have been extensively characterized, our understanding of the underlying causes remains incomplete. Here, we investigated the nutrient fluxes and the physiological as well as molecular responses of the widespread coral Stylophora pistillata to heat stress prior to the onset of bleaching to identify processes involved in the breakdown of the coral–algal symbiosis. We show that altered nutrient cycling during heat stress is a primary driver of the functional breakdown of the symbiosis. Heat stress increased the metabolic energy demand of the coral host, which was compensated by the catabolic degradation of amino acids. The resulting shift from net uptake to release of ammonium by the coral holobiont subsequently promoted the growth of algal symbionts and retention of photosynthates. Together, these processes form a feedback loop that will gradually lead to the decoupling of carbon translocation from the symbiont to the host. Energy limitation and altered symbiotic nutrient cycling are thus key factors in the early heat stress response, directly contributing to the breakdown of the coral–algal symbiosis. Interpreting the stability of the coral holobiont in light of its metabolic interactions provides a missing link in our understanding of the environmental drivers of bleaching and may ultimately help uncover fundamental processes underpinning the functioning of endosymbioses in general.
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spelling pubmed-78651472021-02-17 Heat stress destabilizes symbiotic nutrient cycling in corals Rädecker, Nils Pogoreutz, Claudia Gegner, Hagen M. Cárdenas, Anny Roth, Florian Bougoure, Jeremy Guagliardo, Paul Wild, Christian Pernice, Mathieu Raina, Jean-Baptiste Meibom, Anders Voolstra, Christian R. Proc Natl Acad Sci U S A Biological Sciences Recurrent mass bleaching events are pushing coral reefs worldwide to the brink of ecological collapse. While the symptoms and consequences of this breakdown of the coral–algal symbiosis have been extensively characterized, our understanding of the underlying causes remains incomplete. Here, we investigated the nutrient fluxes and the physiological as well as molecular responses of the widespread coral Stylophora pistillata to heat stress prior to the onset of bleaching to identify processes involved in the breakdown of the coral–algal symbiosis. We show that altered nutrient cycling during heat stress is a primary driver of the functional breakdown of the symbiosis. Heat stress increased the metabolic energy demand of the coral host, which was compensated by the catabolic degradation of amino acids. The resulting shift from net uptake to release of ammonium by the coral holobiont subsequently promoted the growth of algal symbionts and retention of photosynthates. Together, these processes form a feedback loop that will gradually lead to the decoupling of carbon translocation from the symbiont to the host. Energy limitation and altered symbiotic nutrient cycling are thus key factors in the early heat stress response, directly contributing to the breakdown of the coral–algal symbiosis. Interpreting the stability of the coral holobiont in light of its metabolic interactions provides a missing link in our understanding of the environmental drivers of bleaching and may ultimately help uncover fundamental processes underpinning the functioning of endosymbioses in general. National Academy of Sciences 2021-02-02 2021-01-26 /pmc/articles/PMC7865147/ /pubmed/33500354 http://dx.doi.org/10.1073/pnas.2022653118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Rädecker, Nils
Pogoreutz, Claudia
Gegner, Hagen M.
Cárdenas, Anny
Roth, Florian
Bougoure, Jeremy
Guagliardo, Paul
Wild, Christian
Pernice, Mathieu
Raina, Jean-Baptiste
Meibom, Anders
Voolstra, Christian R.
Heat stress destabilizes symbiotic nutrient cycling in corals
title Heat stress destabilizes symbiotic nutrient cycling in corals
title_full Heat stress destabilizes symbiotic nutrient cycling in corals
title_fullStr Heat stress destabilizes symbiotic nutrient cycling in corals
title_full_unstemmed Heat stress destabilizes symbiotic nutrient cycling in corals
title_short Heat stress destabilizes symbiotic nutrient cycling in corals
title_sort heat stress destabilizes symbiotic nutrient cycling in corals
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7865147/
https://www.ncbi.nlm.nih.gov/pubmed/33500354
http://dx.doi.org/10.1073/pnas.2022653118
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