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Variation and Profile of Paralytic Shellfish Poisoning Toxins in Jinhae Bay, Korea

  • Mok, Jong-Soo (Southeast Sea Fisheries Research Institute, National Fisheries Research and Development Institute) ;
  • Song, Ki-Cheol (West Sea Fisheries Research Institute, National Fisheries Research and Development Institute) ;
  • Lee, Ka-Jeong (Food and Safety Research Division, National Fisheries Research and Development Institute) ;
  • Kim, Ji-Hoe (Food and Safety Research Division, National Fisheries Research and Development Institute)
  • Received : 2013.05.22
  • Accepted : 2013.07.16
  • Published : 2013.09.30

Abstract

To understand critical aspects of paralytic shellfish poisoning (PSP) in a chief area of bivalve production in Korea, seasonal variation in PSP toxins in bivalves collected from Jinhae Bay, Korea in 2009 was surveyed by the pre-column high-performance liquid chromatography oxidation method. We also confirmed the profiles of major bivalves such as oysters Crassostrea gigas and mussels Mytilus galloprovincialis in Jinhae Bay. PSP toxins in the bivalves showed remarkable seasonal variation. PSP toxin levels were detected from April to May in 2009, and the highest total toxin levels at all stations were recorded in May. The major toxins in bivalves were gonyautoxin [GTX] 1&4 and C 1&2; in oysters GTX 2&3 were also detected as major components. GTX 1&4, which showed the highest PSP toxin levels at each station, accounted for the highest proportions of toxin components in mussels and oysters (64.5-71.3% and 41.4-42.4%, respectively). It was also confirmed that the highest toxicity (in ${\mu}g$ saxitoxin [STX] eq/g) was derived from GTX 1&4. The highest total toxicity (in ${\mu}g$ STX eq/g) was approximately 2-8-fold higher in mussels than in oysters collected from the same station. PSP toxin levels in bivalves differed significantly according to the sample collection station. However, the profiles of toxins in the bivalves did not show significant differences during the survey period according to sample collection station. This study shows that PSP toxin levels in some samples from Jinhae Bay were above the regulatory limit in Korea during a specific period in spring.

Keywords

References

  1. Chang DS, Shin IS, Pyeun JH and Park YH. 1987. A Study on paralytic shellfish poison of sea mussel, Mytilus edulis. Food poisoning accident in Gamchun Bay, Pusan, Korea, 1986. Bull Korean Fish Soc 20, 293-299.
  2. Chang DS, Shin IS, Kim JH, Pyun JH and Choe WK. 1989. Detoxification of PSP and relationship between PSP toxicity and Protogonyaulax sp. Bull Korean Fish Soc 22, 177-188.
  3. Determan M. 2003. Paralytic Shellfish Poisoning (PSP) Patterns in Puget Sound Shellfish in 2001. Washington State Department of Health, Olympia, WA, US, pp. 1-12.
  4. Edebo L, Lange S, Li XP, Allenmark S, Lindgren K and Thompson R. 1988. Seasonal, geographic, and individual variation of okadaic acid content in cultivated mussels in Sweden. APMIS 96, 1036-1042. https://doi.org/10.1111/j.1699-0463.1988.tb00978.x
  5. Indrasena WM and Gill TA. 2000. Thermal degradation of partially purified paralytic shellfish poison toxins at different times, temperatures and pH. J Food Sci 65, 948-953. http://dx.doi.org/10.1111/j.1365-2621.2000.tb09398.x.
  6. Lawrence JF and Niedzwiadek B. 2001. Quantitative determination of paralytic shellfish poisoning toxins in shellfish using prechromatographic oxidation and liquid chromatography with fluorescence detection. J AOAC Int 84, 1099-1108.
  7. Lee HO, Choi KH and Han MS. 2003. Spring bloom of Alexandrium tamarense in Chinhae Bay, Korea. Aquat Microb Ecol 33, 271-278. http://dx.doi.org/10.3354/ame033271.
  8. Lee JS, Shin IS, Kim YM and Chang DS. 1997. Paralytic shellfish toxins in the mussel, Mytilus edulis, caused the shellfish poisoning accident at Geoje, Korea, in 1996. J Korean Fish Soc 30, 158-160.
  9. Lee KJ, Mok JS, Song KC, Yu HS, Jung JH and Kim JH. 2011. Geographical and annual variation in lipophilic shellfish toxins from oysters and mussels along the south coast of Korea. J Food Prot 74, 2127-2133. http://dx.doi.org/10.4315/0362-028X.JFP-11-148.
  10. Mizuta M, Yamada K, Takata K, Shimaoka M, Takayama H and Ouchi A. 1999. Differences of accumulation and elimination of paralytic shellfish poisons among oyster, mussel and scallop. J Food Hyg Soc Jpn 40, 19-22. http://dx.doi.org/10.3358/shokueishi.40.19.
  11. Mok JS, Oh EG, Son KT, Lee TS, Lee KJ, Song KC and Kim JH. 2012. Accumulation and depuration of paralytic shellfish poison in marine organisms. Korean J Fish Aquat Sci 45, 465-471. http://dx.doi.org/10.5657/KFAS.2012.0465.
  12. Mok JS, Song KC, Lee KJ and Kim JH. 2013. Validation of precolumn HPLC oxidation method for analysis of paralytic shellfish poison. Korean J Fish Aquat Sci 46, 147-153. http://dx.doi.org/10.5657/KFAS.2013.0147.
  13. Noguchi T. 2003. Marine toxins. Nippon Suisan Gakkaishi 69, 895-909. http://dx.doi.org/10.2331/suisan.69.895.
  14. Park MJ, Lee HJ, Lee TS, Son KT, Byun HS, Park JH and Jang DS. 2000. Comparison of paralytic shellfish poison contents and components in the different bivalve species. J Food Hyg Saf 15, 293-296.
  15. Pawiro S. 2010. Bivalves: global production and trade trends. In: Safe Management of Shellfish and Harvest Waters. Rees G, Pond K, Kay D, Bartram J and Domingo JS, eds. World Health Organization, IWA Publishing, London, GB, pp. 11-19.
  16. Rees G, Bartram J and Kay D. 2010. Expert consensus. In: Safe Management of Shellfish and Harvest Waters. Rees G, Pond K, Kay D, Bartram J and Domingo JS, eds. World Health Organization, IWA Publishing, London, GB, pp. 1-10.
  17. Rourke WA, Murphy CJ, Pitcher G, van de Riet JM, Burns BG, Thomas KM and Quilliam MA. 2008. Rapid postcolumn methodology for determination of paralytic shellfish toxins in shellfish tissue. J AOAC Int 91, 589-597.
  18. Shon MB, Kim YS and Kim CR. 2009. Paralytic shellfish poisoning of Mediterranean mussels from Jinhae Bay in Korea. Korean J Fish Aquat Sci 42, 366-372. http://dx.doi.org/10.5657/KFAS.2009.42.4.366.
  19. Silvert W and Subba Rao DV. 1992. Dynamic model of the flux of domoic acid, a neurotoxin, through a Mytilus edulis population. Can J Fish Aquat Sci 49, 400-405. http://dx.doi.org/10.1139/f92-045.
  20. Toyofuku H. 2006. Joint FAO/WHO/IOC activities to provide scientific advice on marine biotoxins (research report). Mar Pollut Bull 52, 1735-1745. http://dx.doi.org/10.1016/j.marpolbul.2006.07.007.
  21. Wekell JC, Hurst J and Lefebvre KA. 2004. The origin of regulatory limits for PSP and ASP toxins in shellfish. J Shellfish Res 23, 927-930.