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Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen

Metabolic interactions with endosymbiotic photosynthetic dinoflagellate Symbiodinium spp. are fundamental to reef-building corals (Scleractinia) thriving in nutrient-poor tropical seas. Yet, detailed understanding at the single-cell level of nutrient assimilation, translocation, and utilization with...

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Autores principales: Kopp, C., Pernice, M., Domart-Coulon, I., Djediat, C., Spangenberg, J. E., Alexander, D. T. L., Hignette, M., Meziane, T., Meibom, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656441/
https://www.ncbi.nlm.nih.gov/pubmed/23674611
http://dx.doi.org/10.1128/mBio.00052-13
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author Kopp, C.
Pernice, M.
Domart-Coulon, I.
Djediat, C.
Spangenberg, J. E.
Alexander, D. T. L.
Hignette, M.
Meziane, T.
Meibom, A.
author_facet Kopp, C.
Pernice, M.
Domart-Coulon, I.
Djediat, C.
Spangenberg, J. E.
Alexander, D. T. L.
Hignette, M.
Meziane, T.
Meibom, A.
author_sort Kopp, C.
collection PubMed
description Metabolic interactions with endosymbiotic photosynthetic dinoflagellate Symbiodinium spp. are fundamental to reef-building corals (Scleractinia) thriving in nutrient-poor tropical seas. Yet, detailed understanding at the single-cell level of nutrient assimilation, translocation, and utilization within this fundamental symbiosis is lacking. Using pulse-chase (15)N labeling and quantitative ion microprobe isotopic imaging (NanoSIMS; nanoscale secondary-ion mass spectrometry), we visualized these dynamic processes in tissues of the symbiotic coral Pocillopora damicornis at the subcellular level. Assimilation of ammonium, nitrate, and aspartic acid resulted in rapid incorporation of nitrogen into uric acid crystals (after ~45 min), forming temporary N storage sites within the dinoflagellate endosymbionts. Subsequent intracellular remobilization of this metabolite was accompanied by translocation of nitrogenous compounds to the coral host, starting at ~6 h. Within the coral tissue, nitrogen is utilized in specific cellular compartments in all four epithelia, including mucus chambers, Golgi bodies, and vesicles in calicoblastic cells. Our study shows how nitrogen-limited symbiotic corals take advantage of sudden changes in nitrogen availability; this opens new perspectives for functional studies of nutrient storage and remobilization in microbial symbioses in changing reef environments.
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spelling pubmed-36564412013-05-17 Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen Kopp, C. Pernice, M. Domart-Coulon, I. Djediat, C. Spangenberg, J. E. Alexander, D. T. L. Hignette, M. Meziane, T. Meibom, A. mBio Research Article Metabolic interactions with endosymbiotic photosynthetic dinoflagellate Symbiodinium spp. are fundamental to reef-building corals (Scleractinia) thriving in nutrient-poor tropical seas. Yet, detailed understanding at the single-cell level of nutrient assimilation, translocation, and utilization within this fundamental symbiosis is lacking. Using pulse-chase (15)N labeling and quantitative ion microprobe isotopic imaging (NanoSIMS; nanoscale secondary-ion mass spectrometry), we visualized these dynamic processes in tissues of the symbiotic coral Pocillopora damicornis at the subcellular level. Assimilation of ammonium, nitrate, and aspartic acid resulted in rapid incorporation of nitrogen into uric acid crystals (after ~45 min), forming temporary N storage sites within the dinoflagellate endosymbionts. Subsequent intracellular remobilization of this metabolite was accompanied by translocation of nitrogenous compounds to the coral host, starting at ~6 h. Within the coral tissue, nitrogen is utilized in specific cellular compartments in all four epithelia, including mucus chambers, Golgi bodies, and vesicles in calicoblastic cells. Our study shows how nitrogen-limited symbiotic corals take advantage of sudden changes in nitrogen availability; this opens new perspectives for functional studies of nutrient storage and remobilization in microbial symbioses in changing reef environments. American Society of Microbiology 2013-05-14 /pmc/articles/PMC3656441/ /pubmed/23674611 http://dx.doi.org/10.1128/mBio.00052-13 Text en Copyright © 2013 Kopp et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kopp, C.
Pernice, M.
Domart-Coulon, I.
Djediat, C.
Spangenberg, J. E.
Alexander, D. T. L.
Hignette, M.
Meziane, T.
Meibom, A.
Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen
title Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen
title_full Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen
title_fullStr Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen
title_full_unstemmed Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen
title_short Highly Dynamic Cellular-Level Response of Symbiotic Coral to a Sudden Increase in Environmental Nitrogen
title_sort highly dynamic cellular-level response of symbiotic coral to a sudden increase in environmental nitrogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656441/
https://www.ncbi.nlm.nih.gov/pubmed/23674611
http://dx.doi.org/10.1128/mBio.00052-13
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