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Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis

BACKGROUND: The coral-Symbiodiniaceae symbiosis is fundamental for the coral reef ecosystem. Corals provide various inorganic nutrients to their algal symbionts in exchange for the photosynthates to meet their metabolic demands. When becoming symbionts, Symbiodiniaceae cells show a reduced prolifera...

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Autores principales: Cui, Guoxin, Liew, Yi Jin, Konciute, Migle K., Zhan, Ye, Hung, Shiou-Han, Thistle, Jana, Gastoldi, Lucia, Schmidt-Roach, Sebastian, Dekker, Job, Aranda, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102920/
https://www.ncbi.nlm.nih.gov/pubmed/35549698
http://dx.doi.org/10.1186/s12915-022-01306-2
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author Cui, Guoxin
Liew, Yi Jin
Konciute, Migle K.
Zhan, Ye
Hung, Shiou-Han
Thistle, Jana
Gastoldi, Lucia
Schmidt-Roach, Sebastian
Dekker, Job
Aranda, Manuel
author_facet Cui, Guoxin
Liew, Yi Jin
Konciute, Migle K.
Zhan, Ye
Hung, Shiou-Han
Thistle, Jana
Gastoldi, Lucia
Schmidt-Roach, Sebastian
Dekker, Job
Aranda, Manuel
author_sort Cui, Guoxin
collection PubMed
description BACKGROUND: The coral-Symbiodiniaceae symbiosis is fundamental for the coral reef ecosystem. Corals provide various inorganic nutrients to their algal symbionts in exchange for the photosynthates to meet their metabolic demands. When becoming symbionts, Symbiodiniaceae cells show a reduced proliferation rate and a different life history. While it is generally believed that the animal hosts play critical roles in regulating these processes, far less is known about the molecular underpinnings that allow the corals to induce the changes in their symbionts. RESULTS: We tested symbiont cell proliferation and life stage changes in vitro in response to different nutrient-limiting conditions to determine the key nutrients and to compare the respective symbiont transcriptomic profiles to cells in hospite. We then examined the effects of nutrient repletion on symbiont proliferation in coral hosts and quantified life stage transitions in vitro using time-lapse confocal imaging. Here, we show that symbionts in hospite share gene expression and pathway activation profiles with free-living cells under nitrogen-limited conditions, strongly suggesting that symbiont proliferation in symbiosis is limited by nitrogen availability. CONCLUSIONS: We demonstrate that nitrogen limitation not only suppresses cell proliferation but also life stage transition to maintain symbionts in the immobile coccoid stage. Nutrient repletion experiments in corals further confirmed that nitrogen availability is the major factor limiting symbiont density in hospite. Our study emphasizes the importance of nitrogen in coral-algae interactions and, more importantly, sheds light on the crucial role of nitrogen in symbiont life history regulation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01306-2.
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spelling pubmed-91029202022-05-14 Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis Cui, Guoxin Liew, Yi Jin Konciute, Migle K. Zhan, Ye Hung, Shiou-Han Thistle, Jana Gastoldi, Lucia Schmidt-Roach, Sebastian Dekker, Job Aranda, Manuel BMC Biol Research Article BACKGROUND: The coral-Symbiodiniaceae symbiosis is fundamental for the coral reef ecosystem. Corals provide various inorganic nutrients to their algal symbionts in exchange for the photosynthates to meet their metabolic demands. When becoming symbionts, Symbiodiniaceae cells show a reduced proliferation rate and a different life history. While it is generally believed that the animal hosts play critical roles in regulating these processes, far less is known about the molecular underpinnings that allow the corals to induce the changes in their symbionts. RESULTS: We tested symbiont cell proliferation and life stage changes in vitro in response to different nutrient-limiting conditions to determine the key nutrients and to compare the respective symbiont transcriptomic profiles to cells in hospite. We then examined the effects of nutrient repletion on symbiont proliferation in coral hosts and quantified life stage transitions in vitro using time-lapse confocal imaging. Here, we show that symbionts in hospite share gene expression and pathway activation profiles with free-living cells under nitrogen-limited conditions, strongly suggesting that symbiont proliferation in symbiosis is limited by nitrogen availability. CONCLUSIONS: We demonstrate that nitrogen limitation not only suppresses cell proliferation but also life stage transition to maintain symbionts in the immobile coccoid stage. Nutrient repletion experiments in corals further confirmed that nitrogen availability is the major factor limiting symbiont density in hospite. Our study emphasizes the importance of nitrogen in coral-algae interactions and, more importantly, sheds light on the crucial role of nitrogen in symbiont life history regulation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01306-2. BioMed Central 2022-05-13 /pmc/articles/PMC9102920/ /pubmed/35549698 http://dx.doi.org/10.1186/s12915-022-01306-2 Text en © The Author(s) 2022 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 Article
Cui, Guoxin
Liew, Yi Jin
Konciute, Migle K.
Zhan, Ye
Hung, Shiou-Han
Thistle, Jana
Gastoldi, Lucia
Schmidt-Roach, Sebastian
Dekker, Job
Aranda, Manuel
Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis
title Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis
title_full Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis
title_fullStr Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis
title_full_unstemmed Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis
title_short Nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis
title_sort nutritional control regulates symbiont proliferation and life history in coral-dinoflagellate symbiosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102920/
https://www.ncbi.nlm.nih.gov/pubmed/35549698
http://dx.doi.org/10.1186/s12915-022-01306-2
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