4.7 Article

Structural Characterization of Maitotoxins Produced by Toxic Gambierdiscus Species

期刊

MARINE DRUGS
卷 20, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/md20070453

关键词

ciguatera poisoning; mass spectrometry; nuclear magnetic resonance spectroscopy; dinoflagellate; benthic; bioassay; acute toxicity

资金

  1. New Zealand Food Safety Science and Research Centre
  2. Cawthron Institute Capability Investment Fund
  3. Seafood Safety research programme [CAWX1801]
  4. Research Council of Norway through the Norwegian NMR platform NNP [139593/140]
  5. National Research Council of Canada

向作者/读者索取更多资源

Identifying compounds responsible for toxicity in Gambierdiscus species is crucial in determining their role in ciguatera poisoning. Two new MTX analogs, MTX-6 and MTX-7, were isolated from G. cheloniae CAWD232 and G. honu CAWD242, respectively. This study provides the most extensive structural characterization of an MTX analog since the complete structure of MTX-1 in 1993.
Identifying compounds responsible for the observed toxicity of the Gambierdiscus species is a critical step to ascertaining whether they contribute to ciguatera poisoning. Macroalgae samples were collected during research expeditions to Rarotonga (Cook Islands) and North Meyer Island (Kermadec Islands), from which two new Gambierdiscus species were characterized, G. cheloniae CAWD232 and G. honu CAWD242. Previous chemical and toxicological investigations of these species demonstrated that they did not produce the routinely monitored Pacific ciguatoxins nor maitotoxin-1 (MTX-1), yet were highly toxic to mice via intraperitoneal (i.p.) injection. Bioassay-guided fractionation of methanolic extracts, incorporating wet chemistry and chromatographic techniques, was used to isolate two new MTX analogs; MTX-6 from G. cheloniae CAWD232 and MTX-7 from G. honu CAWD242. Structural characterization of the new MTX analogs used a combination of analytical chemistry techniques, including LC-MS, LC-MS/MS, HR-MS, oxidative cleavage and reduction, and NMR spectroscopy. A substantial portion of the MTX-7 structure was elucidated, and (to a lesser extent) that of MTX-6. Key differences from MTX-1 included monosulfation, additional hydroxyl groups, an extra double bond, and in the case of MTX-7, an additional methyl group. To date, this is the most extensive structural characterization performed on an MTX analog since the complete structure of MTX-1 was published in 1993. MTX-7 was extremely toxic to mice via i.p. injection (LD50 of 0.235 mu g/kg), although no toxicity was observed at the highest dose rate via oral administration (155.8 mu g/kg). Future research is required to investigate the bioaccumulation and likely biotransformation of the MTX analogs in the marine food web.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据