Abstract

Concentrations of the paralytic shellfish toxins GTX6, C1+2, GTX5, C3+4, dcSTX, dcNEO and dcGTX2+3 were determined by LC-FLD in composite samples of whole soft tissues of mussels (Mytilus galloprovincialis), cockles (Cerastoderma edule) and razor shells (Solen marginatus) after exposure to a Gymnodinium catenatum bloom. Specimens were harvested weekly during three months under natural depuration conditions in the Mira branch of Aveiro lagoon, Portugal. Under the decline of G. catenatum cell densities, elimination or transformation of the uptake toxins associated with the ingestion of toxic cells differed among the surveyed species. Ratio between the toxins dcSTX plus dcGTX2+3 plus dcNEO and toxins GTX6 plus GTX5 plus C1+2 plus C3+4 was used to illustrate the biotransformation occurring in the bivalves. Enhancement of the ratios was observed for razor shells and cockles seven weeks after the peak of the algal bloom. Most likely it reflects more intense biotransformation in razor shells and cockles than in mussels. Conversion into toxins of higher toxicity may prolong the bivalve toxicity. These results show the complexity of toxin elimination in bivalves under post-bloom conditions and emphasize the pertinence of monitoring programs of bivalve toxicity in order to protect human health.

Highlights

  • Paralytic shellfish toxins (PST) are neurotoxic alkaloyds naturally produced by marine dinoflagellates belonging to the genera Alexandrium, Gymnodinium and Pyrodinium (Gedaria et al, 2007; Krock et al, 2007)

  • Gymnodinium catenatum was the PST-producer species as it has been reported in previous works in Portugal (Botelho et al, 2019)

  • The results showed higher proportion of C1+2 in cockles (34%) than in mussels (24%) and in razor shells (16%), while the compound GTX5 reached 24% in razor shells, clearly above the 13% in mussels and 11% in cockles

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Summary

Introduction

Paralytic shellfish toxins (PST) are neurotoxic alkaloyds naturally produced by marine dinoflagellates belonging to the genera Alexandrium, Gymnodinium and Pyrodinium (Gedaria et al, 2007; Krock et al, 2007). This group of toxins comprises a vast range of saxitoxin derivatives. Bivalves as filter feeding organisms may accumulate and biotransform those compounds in their tissues during toxic algal blooms (Bricelj and Shumway, 1998). Oshima (1995b) proposed PSTs transformation pathways in shellfish tissues (Figure 1). As result of the balance among uptake of ingested toxins, biotransformation and elimination processes, consumption of contaminated bivalves may represent a serious risk for human health (Arnich and Thébault, 2018; García et al, 2005; Gessner et al, 1997)

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