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Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates

SIMPLE SUMMARY: The invasive red seaweed Asparagopsis armata exhibits a strong invasive behavior, producing harmful secondary metabolites that negatively affect the surrounding community. This study addressed the antioxidant defenses, oxidative damage, and a neuronal parameter, as well as the fatty...

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Autores principales: Silva, Carla O., Simões, Tiago, Félix, Rafael, Soares, Amadeu M.V.M., Barata, Carlos, Novais, Sara C., Lemos, Marco F.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002046/
https://www.ncbi.nlm.nih.gov/pubmed/33799463
http://dx.doi.org/10.3390/biology10030223
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author Silva, Carla O.
Simões, Tiago
Félix, Rafael
Soares, Amadeu M.V.M.
Barata, Carlos
Novais, Sara C.
Lemos, Marco F.L.
author_facet Silva, Carla O.
Simões, Tiago
Félix, Rafael
Soares, Amadeu M.V.M.
Barata, Carlos
Novais, Sara C.
Lemos, Marco F.L.
author_sort Silva, Carla O.
collection PubMed
description SIMPLE SUMMARY: The invasive red seaweed Asparagopsis armata exhibits a strong invasive behavior, producing harmful secondary metabolites that negatively affect the surrounding community. This study addressed the antioxidant defenses, oxidative damage, and a neuronal parameter, as well as the fatty acid composition responses to sublethal concentrations of A. armata released compounds on the marine snail Gibbula umbilicalis and the shrimp Palaemon serratus. Results revealed that the test species had different metabolic responses to the A. armata exudate concentrations tested. Impacts in G. umbilicalis does not seem to arise from oxidative stress or neurotoxicity, while for P. elegans, an inhibition of AChE and the decrease of antioxidant capacity and increase of LPO suggest neurotoxicity and oxidative stress as contributing to the observed toxicity. Additionally, there were different fatty acid profile changes between species, but omega-3 PUFAs ARA and DPA increased in both invertebrates, indicating a common regulation mechanism of inflammation and immunity responses. ABSTRACT: The seaweed Asparagopsis armata exhibits a strong invasive behavior, producing halogenated compounds with effective biological effects. This study addresses the biochemical responses to sublethal concentrations of A. armata exudate on the marine snail Gibbula umbilicalis whole body and the shrimp Palaemon elegans eyes and hepatopancreas. Antioxidant defenses superoxide dismutase (SOD) and glutathione-S-transferase (GST), oxidative damage endpoints lipid peroxidation (LPO) and DNA damage, the neuronal parameter acetylcholinesterase (AChE), and the fatty acid profile were evaluated. Results revealed different metabolic responses in both species. Despite previous studies indicating that the exudate affected G. umbilicalis’ survival and behavior, this does not seem to result from oxidative stress or neurotoxicity. For P. elegans, the inhibition of AChE and the decrease of antioxidant capacity is concomitant with the increase of LPO, suggesting neurotoxicity and oxidative stress as contributor mechanisms of toxicity for this species. Fatty acid profile changes were more pronounced for P. elegans with a general increase in polyunsaturated fatty acids (PUFAs) with the exudate exposure, which commonly means a defense mechanism protecting from membrane disruption. Nonetheless, the omega-3 PUFAs arachidonic acid (ARA) and docosapentaenoic acid (DPA) increased in both invertebrates, indicating a common regulation mechanism of inflammation and immunity responses.
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spelling pubmed-80020462021-03-28 Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates Silva, Carla O. Simões, Tiago Félix, Rafael Soares, Amadeu M.V.M. Barata, Carlos Novais, Sara C. Lemos, Marco F.L. Biology (Basel) Article SIMPLE SUMMARY: The invasive red seaweed Asparagopsis armata exhibits a strong invasive behavior, producing harmful secondary metabolites that negatively affect the surrounding community. This study addressed the antioxidant defenses, oxidative damage, and a neuronal parameter, as well as the fatty acid composition responses to sublethal concentrations of A. armata released compounds on the marine snail Gibbula umbilicalis and the shrimp Palaemon serratus. Results revealed that the test species had different metabolic responses to the A. armata exudate concentrations tested. Impacts in G. umbilicalis does not seem to arise from oxidative stress or neurotoxicity, while for P. elegans, an inhibition of AChE and the decrease of antioxidant capacity and increase of LPO suggest neurotoxicity and oxidative stress as contributing to the observed toxicity. Additionally, there were different fatty acid profile changes between species, but omega-3 PUFAs ARA and DPA increased in both invertebrates, indicating a common regulation mechanism of inflammation and immunity responses. ABSTRACT: The seaweed Asparagopsis armata exhibits a strong invasive behavior, producing halogenated compounds with effective biological effects. This study addresses the biochemical responses to sublethal concentrations of A. armata exudate on the marine snail Gibbula umbilicalis whole body and the shrimp Palaemon elegans eyes and hepatopancreas. Antioxidant defenses superoxide dismutase (SOD) and glutathione-S-transferase (GST), oxidative damage endpoints lipid peroxidation (LPO) and DNA damage, the neuronal parameter acetylcholinesterase (AChE), and the fatty acid profile were evaluated. Results revealed different metabolic responses in both species. Despite previous studies indicating that the exudate affected G. umbilicalis’ survival and behavior, this does not seem to result from oxidative stress or neurotoxicity. For P. elegans, the inhibition of AChE and the decrease of antioxidant capacity is concomitant with the increase of LPO, suggesting neurotoxicity and oxidative stress as contributor mechanisms of toxicity for this species. Fatty acid profile changes were more pronounced for P. elegans with a general increase in polyunsaturated fatty acids (PUFAs) with the exudate exposure, which commonly means a defense mechanism protecting from membrane disruption. Nonetheless, the omega-3 PUFAs arachidonic acid (ARA) and docosapentaenoic acid (DPA) increased in both invertebrates, indicating a common regulation mechanism of inflammation and immunity responses. MDPI 2021-03-14 /pmc/articles/PMC8002046/ /pubmed/33799463 http://dx.doi.org/10.3390/biology10030223 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Silva, Carla O.
Simões, Tiago
Félix, Rafael
Soares, Amadeu M.V.M.
Barata, Carlos
Novais, Sara C.
Lemos, Marco F.L.
Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates
title Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates
title_full Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates
title_fullStr Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates
title_full_unstemmed Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates
title_short Asparagopsis armata Exudate Cocktail: The Quest for the Mechanisms of Toxic Action of an Invasive Seaweed on Marine Invertebrates
title_sort asparagopsis armata exudate cocktail: the quest for the mechanisms of toxic action of an invasive seaweed on marine invertebrates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002046/
https://www.ncbi.nlm.nih.gov/pubmed/33799463
http://dx.doi.org/10.3390/biology10030223
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