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A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense

Marine dinoflagellates of the genus Alexandrium are the proximal source of neurotoxins associated with Paralytic Shellfish Poisoning. The production of these toxins, the toxin biosynthesis and, thus, the cellular toxicity can be influenced by abiotic and biotic factors. There is, however, a lack of...

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Autores principales: Wohlrab, Sylke, Iversen, Morten H., John, Uwe
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993940/
https://www.ncbi.nlm.nih.gov/pubmed/21124775
http://dx.doi.org/10.1371/journal.pone.0015039
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author Wohlrab, Sylke
Iversen, Morten H.
John, Uwe
author_facet Wohlrab, Sylke
Iversen, Morten H.
John, Uwe
author_sort Wohlrab, Sylke
collection PubMed
description Marine dinoflagellates of the genus Alexandrium are the proximal source of neurotoxins associated with Paralytic Shellfish Poisoning. The production of these toxins, the toxin biosynthesis and, thus, the cellular toxicity can be influenced by abiotic and biotic factors. There is, however, a lack of substantial evidence concerning the toxins' ecological function such as grazing defense. Waterborne cues from copepods have been previously found to induce a species-specific increase in toxin content in Alexandrium minutum. However, it remains speculative in which context these species-specific responses evolved and if it occurs in other Alexandrium species as well. In this study we exposed Alexandrium tamarense to three copepod species (Calanus helgolandicus, Acartia clausii, and Oithona similis) and their corresponding cues. We show that the species-specific response towards copepod-cues is not restricted to one Alexandrium species and that co-evolutionary processes might be involved in these responses, thus giving additional evidence for the defensive role of phycotoxins. Through a functional genomic approach we gained insights into the underlying molecular processes which could trigger the different outcomes of these species-specific responses and consequently lead to increased toxin content in Alexandrium tamarense. We propose that the regulation of serine/threonine kinase signaling pathways has a major influence in directing the external stimuli i.e. copepod-cues, into different intracellular cascades and networks in A. tamarense. Our results show that A. tamarense can sense potential predating copepods and respond to the received information by increasing its toxin production. Furthermore, we demonstrate how a functional genomic approach can be used to investigate species interactions within the plankton community.
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spelling pubmed-29939402010-12-01 A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense Wohlrab, Sylke Iversen, Morten H. John, Uwe PLoS One Research Article Marine dinoflagellates of the genus Alexandrium are the proximal source of neurotoxins associated with Paralytic Shellfish Poisoning. The production of these toxins, the toxin biosynthesis and, thus, the cellular toxicity can be influenced by abiotic and biotic factors. There is, however, a lack of substantial evidence concerning the toxins' ecological function such as grazing defense. Waterborne cues from copepods have been previously found to induce a species-specific increase in toxin content in Alexandrium minutum. However, it remains speculative in which context these species-specific responses evolved and if it occurs in other Alexandrium species as well. In this study we exposed Alexandrium tamarense to three copepod species (Calanus helgolandicus, Acartia clausii, and Oithona similis) and their corresponding cues. We show that the species-specific response towards copepod-cues is not restricted to one Alexandrium species and that co-evolutionary processes might be involved in these responses, thus giving additional evidence for the defensive role of phycotoxins. Through a functional genomic approach we gained insights into the underlying molecular processes which could trigger the different outcomes of these species-specific responses and consequently lead to increased toxin content in Alexandrium tamarense. We propose that the regulation of serine/threonine kinase signaling pathways has a major influence in directing the external stimuli i.e. copepod-cues, into different intracellular cascades and networks in A. tamarense. Our results show that A. tamarense can sense potential predating copepods and respond to the received information by increasing its toxin production. Furthermore, we demonstrate how a functional genomic approach can be used to investigate species interactions within the plankton community. Public Library of Science 2010-11-29 /pmc/articles/PMC2993940/ /pubmed/21124775 http://dx.doi.org/10.1371/journal.pone.0015039 Text en Wohlrab et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wohlrab, Sylke
Iversen, Morten H.
John, Uwe
A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense
title A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense
title_full A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense
title_fullStr A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense
title_full_unstemmed A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense
title_short A Molecular and Co-Evolutionary Context for Grazer Induced Toxin Production in Alexandrium tamarense
title_sort molecular and co-evolutionary context for grazer induced toxin production in alexandrium tamarense
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993940/
https://www.ncbi.nlm.nih.gov/pubmed/21124775
http://dx.doi.org/10.1371/journal.pone.0015039
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