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MAP Technical Reports Series No. 106 UNEP

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7.2.2.5 DSP compromised seafoods<br />

- 125 -<br />

Causative shellfish in Japan were the mussels Mytilus edulis and M. coruscum, the<br />

scallops Patinopecten yessoensis and Chlamys nipponensis akazara, and the short-necked<br />

clams Tapes japonica and Gomphina melaegis, while in European Atlantic coasts M. edulis and<br />

in Adriatic and French Mediterranean coast M. galloprovincialis. In Japan and in the Atlantic<br />

coast of Spain and France the infestation period ranges from April to September and the highest<br />

toxicity of shellfish is observed from May to August, though it may vary locally (Yasumoto et al.,<br />

1978, 1980, 1984; Campos et al., 1982; Berthomé et al., 1986; Delmas et al., 1993). In<br />

Scandinavia, on the contrary, oysters in February and mussels in October have caused DSP<br />

(Edebo et al., 1988). According to the provisions of the Italian Laws on toxic shellfish (Ministero<br />

della Sanità, 1978; 1990a,b,c) the level of DSP biotoxins present in mussels from intensive<br />

farms and natural beds along the coasts of Emilia-Romagna made them unsuitable for sale for<br />

human consumption for a duration of 8 months (Viviani et al., 1990) for two consecutive periods,<br />

from June 1989 to January 1990 and from June 1990 to January 1991. Okadaic acid and DTX-1<br />

were found in Western European shellfish (Dahl and Yndestad, 1985), while YTX was detected<br />

in <strong>No</strong>rwegian blue mussels in addition to acidic components (Lee et al., 1987). PTXs have not<br />

been reported from European shellfish but few attempts have been made to detect these<br />

components because of lack of routine methodology for their detection (Krogh, 1989). In<br />

hepatopancreas of highly toxic mussels of Adriatic sea the presence of okadaic acid has been<br />

evidenced through 1 H NMR spectroscopy. In addition, structural elucidation of the components<br />

of two further toxic fractions is still in progress (Fattorusso et al., 1992).<br />

The method of cooking did not alter toxicity of the causative shellfish but intoxication<br />

could be avoided if the digestive glands were eliminated beforehand (Yasumoto et al., 1978;<br />

1990). Comparative analysis for DSP in various shellfish collected from the same area was<br />

conducted in Japan and the highest toxicity was found in the blue mussels, with less toxicity in<br />

scallops, and very little in oysters. The differences were noted between mussels cultivated at<br />

different depths, with concentrations differing by factors of two to three (Yasumoto et al., 1978;<br />

1980). Also the first results obtained in the Adriatic sea (Boni et al., 1992) show that not all<br />

species of bivalve molluscs, living in the same habitat infested by the microalgae, manifest an<br />

analogous functional attitude towards the absorption and concentration of the enterotoxin in their<br />

tissues. In particular, although they were drawn out of the same habitat, while values of 4 MU<br />

(calculated according to IFREMER) were found in mussels, in Tapes semidecussatus the risk<br />

level was never passed, in C. gallina, O. edulis and V. verrucosa DSP was not detected.<br />

7.2.2.6 DSP detoxification in bivalve molluscs<br />

Two DSP depuration experiments have been undertaken in 1989: one in laboratory<br />

conditions and the other one in an oyster culture pond (Lassus et al., 1991). Two different sets<br />

of diarrheic toxins (DSP) contaminated mussels have been used, respectively at high (3 MU)<br />

and low (1 MU) initial toxic levels. These two sets were contaminated during two Dinophysis spp.<br />

blooms, which occurred in June 1989 respectively along French Mediterranean (Sete) and West-<br />

Brittany coasts (Douarnenex Bay). Depuration rates have been estimated simultaneously by<br />

mouse test and high pressure liquid chromatography (HPLC). For highly toxic mussels, results<br />

evidence a better depuration rate in the oyster culture pond with 0.5 MU g -1 in digestive glands<br />

after 20 days and 1.0 MU g -1 in laboratory conditions after 42 days. For lower initial toxic level (1<br />

MU), time needed for depuration is of course shorter but similar disparity is observed between<br />

laboratory and pond experiments are assumed to be the causative factors for observed<br />

differences in depuration rates (Lassus et al., 1991).

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