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Lineage-specific symbionts mediate differential coral responses to thermal stress

BACKGROUND: Ocean warming is a leading cause of increasing episodes of coral bleaching, the dissociation between coral hosts and their dinoflagellate algal symbionts in the family Symbiodiniaceae. While the diversity and flexibility of Symbiodiniaceae is presumably responsible for variations in cora...

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Autores principales: Wang, Chenying, Zheng, Xinqing, Kvitt, Hagit, Sheng, Huaxia, Sun, Danye, Niu, Gaofeng, Tchernov, Dan, Shi, Tuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521517/
https://www.ncbi.nlm.nih.gov/pubmed/37752514
http://dx.doi.org/10.1186/s40168-023-01653-4
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author Wang, Chenying
Zheng, Xinqing
Kvitt, Hagit
Sheng, Huaxia
Sun, Danye
Niu, Gaofeng
Tchernov, Dan
Shi, Tuo
author_facet Wang, Chenying
Zheng, Xinqing
Kvitt, Hagit
Sheng, Huaxia
Sun, Danye
Niu, Gaofeng
Tchernov, Dan
Shi, Tuo
author_sort Wang, Chenying
collection PubMed
description BACKGROUND: Ocean warming is a leading cause of increasing episodes of coral bleaching, the dissociation between coral hosts and their dinoflagellate algal symbionts in the family Symbiodiniaceae. While the diversity and flexibility of Symbiodiniaceae is presumably responsible for variations in coral response to physical stressors such as elevated temperature, there is little data directly comparing physiological performance that accounts for symbiont identity associated with the same coral host species. Here, using Pocillopora damicornis harboring genotypically distinct Symbiodiniaceae strains, we examined the physiological responses of the coral holobiont and the dynamics of symbiont community change under thermal stress in a laboratory-controlled experiment. RESULTS: We found that P. damicornis dominated with symbionts of metahaplotype D1-D4-D6 in the genus Durusdinium (i.e., PdD holobiont) was more robust to thermal stress than its counterpart with symbionts of metahaplotype C42-C1-C1b-C1c in the genus Cladocopium (i.e., PdC holobiont). Under ambient temperature, however, the thermally sensitive Cladocopium spp. exhibited higher photosynthetic efficiency and translocated more fixed carbon to the host, likely facilitating faster coral growth and calcification. Moreover, we observed a thermally induced increase in Durusdinium proportion in the PdC holobiont; however, this “symbiont shuffling” in the background was overwhelmed by the overall Cladocopium dominance, which coincided with faster coral bleaching and reduced calcification. CONCLUSIONS: These findings support that lineage-specific symbiont dominance is a driver of distinct coral responses to thermal stress. In addition, we found that “symbiont shuffling” may begin with stress-forced, subtle changes in the rare biosphere to eventually trade off growth for increased resilience. Furthermore, the flexibility in corals’ association with thermally tolerant symbiont lineages to adapt or acclimatize to future warming oceans should be viewed with conservative optimism as the current rate of environmental changes may outpace the evolutionary capabilities of corals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01653-4.
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spelling pubmed-105215172023-09-27 Lineage-specific symbionts mediate differential coral responses to thermal stress Wang, Chenying Zheng, Xinqing Kvitt, Hagit Sheng, Huaxia Sun, Danye Niu, Gaofeng Tchernov, Dan Shi, Tuo Microbiome Research BACKGROUND: Ocean warming is a leading cause of increasing episodes of coral bleaching, the dissociation between coral hosts and their dinoflagellate algal symbionts in the family Symbiodiniaceae. While the diversity and flexibility of Symbiodiniaceae is presumably responsible for variations in coral response to physical stressors such as elevated temperature, there is little data directly comparing physiological performance that accounts for symbiont identity associated with the same coral host species. Here, using Pocillopora damicornis harboring genotypically distinct Symbiodiniaceae strains, we examined the physiological responses of the coral holobiont and the dynamics of symbiont community change under thermal stress in a laboratory-controlled experiment. RESULTS: We found that P. damicornis dominated with symbionts of metahaplotype D1-D4-D6 in the genus Durusdinium (i.e., PdD holobiont) was more robust to thermal stress than its counterpart with symbionts of metahaplotype C42-C1-C1b-C1c in the genus Cladocopium (i.e., PdC holobiont). Under ambient temperature, however, the thermally sensitive Cladocopium spp. exhibited higher photosynthetic efficiency and translocated more fixed carbon to the host, likely facilitating faster coral growth and calcification. Moreover, we observed a thermally induced increase in Durusdinium proportion in the PdC holobiont; however, this “symbiont shuffling” in the background was overwhelmed by the overall Cladocopium dominance, which coincided with faster coral bleaching and reduced calcification. CONCLUSIONS: These findings support that lineage-specific symbiont dominance is a driver of distinct coral responses to thermal stress. In addition, we found that “symbiont shuffling” may begin with stress-forced, subtle changes in the rare biosphere to eventually trade off growth for increased resilience. Furthermore, the flexibility in corals’ association with thermally tolerant symbiont lineages to adapt or acclimatize to future warming oceans should be viewed with conservative optimism as the current rate of environmental changes may outpace the evolutionary capabilities of corals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01653-4. BioMed Central 2023-09-26 /pmc/articles/PMC10521517/ /pubmed/37752514 http://dx.doi.org/10.1186/s40168-023-01653-4 Text en © The Author(s) 2023 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 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
Wang, Chenying
Zheng, Xinqing
Kvitt, Hagit
Sheng, Huaxia
Sun, Danye
Niu, Gaofeng
Tchernov, Dan
Shi, Tuo
Lineage-specific symbionts mediate differential coral responses to thermal stress
title Lineage-specific symbionts mediate differential coral responses to thermal stress
title_full Lineage-specific symbionts mediate differential coral responses to thermal stress
title_fullStr Lineage-specific symbionts mediate differential coral responses to thermal stress
title_full_unstemmed Lineage-specific symbionts mediate differential coral responses to thermal stress
title_short Lineage-specific symbionts mediate differential coral responses to thermal stress
title_sort lineage-specific symbionts mediate differential coral responses to thermal stress
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521517/
https://www.ncbi.nlm.nih.gov/pubmed/37752514
http://dx.doi.org/10.1186/s40168-023-01653-4
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