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The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid

The polyether toxin, okadaic acid, causes diarrhetic shellfish poisoning in humans. Despite extensive research into its cellular targets using rodent models, we know little about its putative effect(s) on innate immunity. We inoculated larvae of the greater wax moth, Galleria mellonella, with physio...

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Autores principales: Coates, Christopher J., Lim, Jenson, Harman, Katie, Rowley, Andrew F., Griffiths, David J., Emery, Helena, Layton, Will
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556153/
https://www.ncbi.nlm.nih.gov/pubmed/30426330
http://dx.doi.org/10.1007/s10565-018-09448-2
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author Coates, Christopher J.
Lim, Jenson
Harman, Katie
Rowley, Andrew F.
Griffiths, David J.
Emery, Helena
Layton, Will
author_facet Coates, Christopher J.
Lim, Jenson
Harman, Katie
Rowley, Andrew F.
Griffiths, David J.
Emery, Helena
Layton, Will
author_sort Coates, Christopher J.
collection PubMed
description The polyether toxin, okadaic acid, causes diarrhetic shellfish poisoning in humans. Despite extensive research into its cellular targets using rodent models, we know little about its putative effect(s) on innate immunity. We inoculated larvae of the greater wax moth, Galleria mellonella, with physiologically relevant doses of okadaic acid by direct injection into the haemocoel (body cavity) and/or gavage (force-feeding). We monitored larval survival and employed a range of cellular and biochemical assays to assess the potential harmful effects of okadaic acid. Okadaic acid at concentrations ≥ 75 ng/larva (≥ 242 μg/kg) led to significant reductions in larval survival (> 65%) and circulating haemocyte (blood cell) numbers (> 50%) within 24 h post-inoculation. In the haemolymph, okadaic acid reduced haemocyte viability and increased phenoloxidase activities. In the midgut, okadaic acid induced oxidative damage as determined by increases in superoxide dismutase activity and levels of malondialdehyde (i.e. lipid peroxidation). Our observations of insect larvae correspond broadly to data published using rodent models of shellfish-poisoning toxidrome, including complementary LD(50) values: 206–242 μg/kg in mice, ~ 239 μg/kg in G. mellonella. These data support the use of this insect as a surrogate model for the investigation of marine toxins, which offers distinct ethical and financial incentives. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-018-09448-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-65561532019-06-21 The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid Coates, Christopher J. Lim, Jenson Harman, Katie Rowley, Andrew F. Griffiths, David J. Emery, Helena Layton, Will Cell Biol Toxicol Original Article The polyether toxin, okadaic acid, causes diarrhetic shellfish poisoning in humans. Despite extensive research into its cellular targets using rodent models, we know little about its putative effect(s) on innate immunity. We inoculated larvae of the greater wax moth, Galleria mellonella, with physiologically relevant doses of okadaic acid by direct injection into the haemocoel (body cavity) and/or gavage (force-feeding). We monitored larval survival and employed a range of cellular and biochemical assays to assess the potential harmful effects of okadaic acid. Okadaic acid at concentrations ≥ 75 ng/larva (≥ 242 μg/kg) led to significant reductions in larval survival (> 65%) and circulating haemocyte (blood cell) numbers (> 50%) within 24 h post-inoculation. In the haemolymph, okadaic acid reduced haemocyte viability and increased phenoloxidase activities. In the midgut, okadaic acid induced oxidative damage as determined by increases in superoxide dismutase activity and levels of malondialdehyde (i.e. lipid peroxidation). Our observations of insect larvae correspond broadly to data published using rodent models of shellfish-poisoning toxidrome, including complementary LD(50) values: 206–242 μg/kg in mice, ~ 239 μg/kg in G. mellonella. These data support the use of this insect as a surrogate model for the investigation of marine toxins, which offers distinct ethical and financial incentives. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-018-09448-2) contains supplementary material, which is available to authorized users. Springer Netherlands 2018-11-13 2019 /pmc/articles/PMC6556153/ /pubmed/30426330 http://dx.doi.org/10.1007/s10565-018-09448-2 Text en © The Author(s) 2018 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Article
Coates, Christopher J.
Lim, Jenson
Harman, Katie
Rowley, Andrew F.
Griffiths, David J.
Emery, Helena
Layton, Will
The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid
title The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid
title_full The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid
title_fullStr The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid
title_full_unstemmed The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid
title_short The insect, Galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid
title_sort insect, galleria mellonella, is a compatible model for evaluating the toxicology of okadaic acid
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556153/
https://www.ncbi.nlm.nih.gov/pubmed/30426330
http://dx.doi.org/10.1007/s10565-018-09448-2
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