通过生产无毒代谢物去除贝类中的短链毒素:对海产品安全和生物毒素的环境命运的影响。

J Naar, J Kubanek, A Weidner, L Flewelling, A Bourdelais, K Steidinger, D G Baden
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引用次数: 0

摘要

在鞭毛藻短凯伦氏菌大量繁殖期间,牡蛎和蛤蜊等滤食性动物会积累短毒素,通常会达到对人类有毒的水平。在对照水族馆实验中,我们将活牡蛎暴露在有毒的短梭菌中,然后再暴露在无毒的微藻中10周。每周采集牡蛎,分析短叶毒素和短叶毒素代谢物,以量化毒素的生物积累和净化。所有被牡蛎浓缩的PbTx-2立即转化为极性代谢物的混合物,然后从牡蛎中慢慢消除。然而,90%的PbTx-3在毒性暴露两周内被消除,但没有明显的生物转化。腹腔注射含有高水平PbTx-3的牡蛎提取物对小鼠有毒性。去除PbTx-3后收获的牡蛎提取物是无毒的,尽管PbTx-2的代谢物浓度很高。在佛罗里达采集的短链乳杆菌爆发期间和之后的牡蛎含有PbTx-2和PbTx-3的极性代谢物,但不含PbTx-2。再次,PbTx-3浓度是小鼠毒性的一个很好的预测指标。将PbTx-2注入牡蛎或蛤蜊匀浆中,然后在室温下短暂孵育,PbTx-2也能100%转化为极性代谢物。无论是口服还是腹腔注射,这些PbTx-2代谢物都不会杀死小鼠,即使浓度是毒性PbTx-3水平的30倍。
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Brevetoxin Depuration in Shellfish via Production of Non-toxic Metabolites: Consequences for Seafood Safety and the Environmental Fate of Biotoxins.

During blooms of the dinoflagellate Karenia brevis, filter-feeders such as oysters and clams bioaccumulate brevetoxins, often to levels that are toxic to humans. In controlled aquarium experiments, we exposed live oysters to bloom levels of toxic K. brevis, followed by 10 weeks of exposure to non-toxic microalgae. Oysters were harvested weekly and analyzed for brevetoxins and brevetoxin metabolites to quantify toxin bioaccumulation and depuration. All of the PbTx-2 concentrated by oysters was immediately converted to a mixture of polar metabolites that were then slowly eliminated from the oysters. However, 90% of measured PbTx-3 was eliminated within two weeks of toxic exposure but without apparent biotransformation. Extracts of oysters containing high levels of PbTx-3 were toxic to mice by intraperitoneal (IP) injection. Extracts of oysters harvested after PbTx-3 had been eliminated were non-toxic despite high concentrations of PbTx-2 metabolites. Oysters collected in Florida during and after a bloom of K. brevis contained polar metabolites of PbTx-2 as well as PbTx-3, but no PbTx-2. Again, PbTx-3 concentration was a good predictor of mouse toxicity. One hundred percent conversion of PbTx-2 to polar metabolites was also accomplished in vitro by spiking oyster or clam homogenate with PbTx-2, followed by a brief incubation at room temperature. These PbTx-2 metabolites did not kill mice, either orally or by intraperitoneal injection, even at concentrations 30 times greater than toxic PbTx-3 levels.

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Brevetoxin Degradation and By-Product Formation via Natural Sunlight. Competitive ELISA: An Accurate, Quick and Effective Tool to Monitor Brevetoxins in Environmental and Biological Sample. Multi-Laboratory Study of Five Methods for the Determination of Brevetoxins in Shellfish Tissue Extracts. Florida Red Tide: Inhalation Toxicity of Karenia brevis Extract in Rats. An Epidemiologic Approach to the Study of Aerosolized Florida Red Tides.
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