LC-MS/MS Analysis of Cyanotoxins in Bivalve Mollusks—Method Development, Validation and First Evidence of Occurrence of Nodularin in Mussels (Mytilus edulis) and Oysters (Magallana gigas) from the West Coast of Sweden

Author:

España Amórtegui Julio César12ORCID,Pekar Heidi13,Retrato Mark Dennis Chico4ORCID,Persson Malin1,Karlson Bengt5ORCID,Bergquist Jonas4ORCID,Zuberovic-Muratovic Aida14

Affiliation:

1. Science Department, Swedish Food Agency, Box 622, SE-751 26 Uppsala, Sweden

2. Chemistry Department, Science Faculty, Universidad Nacional de Colombia, Cr. 45 N° 26-85, Bogotá P.O. Box 111321, Colombia

3. Stockholm Water and Waste Company, Bryggerivägen 10, SE-106 36 Stockholm, Sweden

4. Department of Chemistry, Biomedical Center, Analytical Chemistry and Neurochemistry, Uppsala University, Box 599, SE-751 24 Uppsala, Sweden

5. Research and Development, Oceanography, Swedish Meteorological and Hydrological Institute, Sven Källfelts Gata 15, SE-426 71 Västra Frölunda, Sweden

Abstract

In this paper, an LC-MS/MS method for the simultaneous identification and quantification of cyanotoxins with hydrophilic and lipophilic properties in edible bivalves is presented. The method includes 17 cyanotoxins comprising 13 microcystins (MCs), nodularin (NOD), anatoxin-a (ATX-a), homoanatoxin (h-ATX) and cylindrospermopsin (CYN). A benefit to the presented method is the possibility for the MS detection of MC-LR-[Dha7] and MC-LR-[Asp3] as separately identified and MS-resolved MRM signals, two congeners which were earlier detected together. The performance of the method was evaluated by in-house validation using spiked mussel samples in the quantification range of 3.12–200 µg/kg. The method was found to be linear over the full calibration range for all included cyanotoxins except CYN for which a quadratic regression was used. The method showed limitations for MC-LF (R2 = 0.94), MC-LA (R2 ≤ 0.98) and MC-LW (R2 ≤ 0.98). The recoveries for ATX-a, h-ATX, CYN, NOD, MC-LF and MC-LW were lower than desired (<70%), but stable. Despite the given limitations, the validation results showed that the method was specific and robust for the investigated parameters. The results demonstrate the suitability of the method to be applied as a reliable monitoring tool for the presented group of cyanotoxins, as well as highlight the compromises that need to be included if multi-toxin methods are to be used for the analysis of cyanotoxins with a broader range of chemical properties. Furthermore, the method was used to analyze 13 samples of mussels (Mytilus edulis) and oysters (Magallana gigas) collected in the 2020–2022 summers along the coast of Bohuslän (Sweden). A complementary qualitative analysis for the presence of cyanotoxins in phytoplankton samples collected from marine waters around southern Sweden was performed with the method. Nodularin was identified in all samples and quantified in bivalve samples in the range of 7–397 µg/kg. Toxins produced by cyanobacteria are not included in the European Union regulatory monitoring of bivalves; thus, the results presented in this study can be useful in providing the basis for future work including cyanotoxins within the frame of regulatory monitoring to increase seafood safety.

Funder

Swedish Foundation For Strategic Research

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Toxicology

Reference63 articles.

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5. Ecogenomics and Taxonomy of Cyanobacteria Phylum;Walter;Front. Microbiol.,2017

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