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Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas

Antifouling biocides such as organotin compounds and their alternatives are potent toxicants in marine ecosystems. In this study, we employed several molecular and biochemical response systems of the Pacific oyster Crassostrea gigas to understand a potential mode of action of antifouling biocides (i...

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Autores principales: Park, Mi Seon, Kim, Young Dae, Kim, Bo-Mi, Kim, Youn-Jung, Kim, Jang Kyun, Rhee, Jae-Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179263/
https://www.ncbi.nlm.nih.gov/pubmed/28006823
http://dx.doi.org/10.1371/journal.pone.0168978
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author Park, Mi Seon
Kim, Young Dae
Kim, Bo-Mi
Kim, Youn-Jung
Kim, Jang Kyun
Rhee, Jae-Sung
author_facet Park, Mi Seon
Kim, Young Dae
Kim, Bo-Mi
Kim, Youn-Jung
Kim, Jang Kyun
Rhee, Jae-Sung
author_sort Park, Mi Seon
collection PubMed
description Antifouling biocides such as organotin compounds and their alternatives are potent toxicants in marine ecosystems. In this study, we employed several molecular and biochemical response systems of the Pacific oyster Crassostrea gigas to understand a potential mode of action of antifouling biocides (i.e. tributyltin (TBT), diuron and irgarol) after exposure to different concentrations (0.01, 0.1, and 1 μg L(-1)) for 96 h. As a result, all the three antifouling biocides strongly induced the antioxidant defense system. TBT reduced both enzymatic activity and mRNA expression of Na(+)/K(+)-ATPase and acetylcholinesterase (AChE). Lower levels of both Na(+)/K(+)-ATPase activity and AChE mRNA expression were observed in the diuron-exposed oysters compared to the control, while the irgarol treatment reduced only the transcriptional expression of AChE gene. We also analyzed transcript profile of heat shock protein (Hsp) superfamily in same experimental conditions. All antifouling biocides tested in this study significantly modulated mRNA expression of Hsp superfamily with strong induction of Hsp70 family. Taken together, overall results indicate that representative organotin TBT and alternatives have potential hazardous effects on the gill of C. gigas within relatively short time period. Our results also suggest that analyzing a series of molecular and biochemical parameters can be a way of understanding and uncovering the mode of action of emerging antifouling biocides. In particular, it was revealed that Pacific oysters have different sensitivities depend on the antifouling biocides.
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spelling pubmed-51792632017-01-04 Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas Park, Mi Seon Kim, Young Dae Kim, Bo-Mi Kim, Youn-Jung Kim, Jang Kyun Rhee, Jae-Sung PLoS One Research Article Antifouling biocides such as organotin compounds and their alternatives are potent toxicants in marine ecosystems. In this study, we employed several molecular and biochemical response systems of the Pacific oyster Crassostrea gigas to understand a potential mode of action of antifouling biocides (i.e. tributyltin (TBT), diuron and irgarol) after exposure to different concentrations (0.01, 0.1, and 1 μg L(-1)) for 96 h. As a result, all the three antifouling biocides strongly induced the antioxidant defense system. TBT reduced both enzymatic activity and mRNA expression of Na(+)/K(+)-ATPase and acetylcholinesterase (AChE). Lower levels of both Na(+)/K(+)-ATPase activity and AChE mRNA expression were observed in the diuron-exposed oysters compared to the control, while the irgarol treatment reduced only the transcriptional expression of AChE gene. We also analyzed transcript profile of heat shock protein (Hsp) superfamily in same experimental conditions. All antifouling biocides tested in this study significantly modulated mRNA expression of Hsp superfamily with strong induction of Hsp70 family. Taken together, overall results indicate that representative organotin TBT and alternatives have potential hazardous effects on the gill of C. gigas within relatively short time period. Our results also suggest that analyzing a series of molecular and biochemical parameters can be a way of understanding and uncovering the mode of action of emerging antifouling biocides. In particular, it was revealed that Pacific oysters have different sensitivities depend on the antifouling biocides. Public Library of Science 2016-12-22 /pmc/articles/PMC5179263/ /pubmed/28006823 http://dx.doi.org/10.1371/journal.pone.0168978 Text en © 2016 Park 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Park, Mi Seon
Kim, Young Dae
Kim, Bo-Mi
Kim, Youn-Jung
Kim, Jang Kyun
Rhee, Jae-Sung
Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas
title Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas
title_full Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas
title_fullStr Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas
title_full_unstemmed Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas
title_short Effects of Antifouling Biocides on Molecular and Biochemical Defense System in the Gill of the Pacific Oyster Crassostrea gigas
title_sort effects of antifouling biocides on molecular and biochemical defense system in the gill of the pacific oyster crassostrea gigas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179263/
https://www.ncbi.nlm.nih.gov/pubmed/28006823
http://dx.doi.org/10.1371/journal.pone.0168978
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