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Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea
Settlement of pelagic coral larvae is commonly induced by chemical cues that originate from biofilms and coralline algae. These natural settlement cues initiate signal pathways leading to attachment and metamorphosis of the coral larva. In order to investigate the settlement process and its natural...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381176/ https://www.ncbi.nlm.nih.gov/pubmed/30783133 http://dx.doi.org/10.1038/s41598-019-38794-2 |
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author | Moeller, Mareen Nietzer, Samuel Schupp, Peter J. |
author_facet | Moeller, Mareen Nietzer, Samuel Schupp, Peter J. |
author_sort | Moeller, Mareen |
collection | PubMed |
description | Settlement of pelagic coral larvae is commonly induced by chemical cues that originate from biofilms and coralline algae. These natural settlement cues initiate signal pathways leading to attachment and metamorphosis of the coral larva. In order to investigate the settlement process and its natural inducers, it is necessary to gain a better understanding of these signal pathways. At present, the pathways and neurotransmitters involved in this signal transduction are still widely unknown. In this study, we exposed larvae of the brooding coral Leptastrea purpurea to five neuroactive compounds known to be present in cnidarians, and K(+) Ions. All compounds were applied at different dilutions and settlement behavior of the larvae was documented over 48 h. Dopamine, glutamic acid and epinephrine significantly induced settlement in the coral larvae. The highest observed metamorphosis response was 54% in 10(−5) M dopamine. Serotonin, L-DOPA and K(+) ions did not have an influence on settlement behavior in our experiments. Exposing larvae to settlement-inducing neurotransmitters and thus bypassing the initial induction could be utilized in coral aquaculture. The active neurotransmitters should be used to further study the settlement process in L. purpurea in greater detail. Their role and relevance should also be assessed for other coral species as they may represent or reveal a universal inducer for coral settlement. |
format | Online Article Text |
id | pubmed-6381176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63811762019-02-22 Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea Moeller, Mareen Nietzer, Samuel Schupp, Peter J. Sci Rep Article Settlement of pelagic coral larvae is commonly induced by chemical cues that originate from biofilms and coralline algae. These natural settlement cues initiate signal pathways leading to attachment and metamorphosis of the coral larva. In order to investigate the settlement process and its natural inducers, it is necessary to gain a better understanding of these signal pathways. At present, the pathways and neurotransmitters involved in this signal transduction are still widely unknown. In this study, we exposed larvae of the brooding coral Leptastrea purpurea to five neuroactive compounds known to be present in cnidarians, and K(+) Ions. All compounds were applied at different dilutions and settlement behavior of the larvae was documented over 48 h. Dopamine, glutamic acid and epinephrine significantly induced settlement in the coral larvae. The highest observed metamorphosis response was 54% in 10(−5) M dopamine. Serotonin, L-DOPA and K(+) ions did not have an influence on settlement behavior in our experiments. Exposing larvae to settlement-inducing neurotransmitters and thus bypassing the initial induction could be utilized in coral aquaculture. The active neurotransmitters should be used to further study the settlement process in L. purpurea in greater detail. Their role and relevance should also be assessed for other coral species as they may represent or reveal a universal inducer for coral settlement. Nature Publishing Group UK 2019-02-19 /pmc/articles/PMC6381176/ /pubmed/30783133 http://dx.doi.org/10.1038/s41598-019-38794-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Moeller, Mareen Nietzer, Samuel Schupp, Peter J. Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea |
title | Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea |
title_full | Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea |
title_fullStr | Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea |
title_full_unstemmed | Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea |
title_short | Neuroactive compounds induce larval settlement in the scleractinian coral Leptastrea purpurea |
title_sort | neuroactive compounds induce larval settlement in the scleractinian coral leptastrea purpurea |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381176/ https://www.ncbi.nlm.nih.gov/pubmed/30783133 http://dx.doi.org/10.1038/s41598-019-38794-2 |
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