Determinación de toxinas paralizantes en el jurel (Trachurus trachurus) durante una proliferación de Gymnodinium catenatum: la prevalencia de decarbamoilsaxitoxina en la red trófica marina

Autores/as

  • Sandra Lage IPMA – Instituto Português do Mar e da Atmosfera
  • Pedro Reis Costa IPMA – Instituto Português do Mar e da Atmosfera

DOI:

https://doi.org/10.3989/scimar.03701.28C

Palabras clave:

toxinas marinas, saxitoxina, peces pelágicos, ficotoxinas, proliferaciones de algas nocivas

Resumen


Este estudio reporta la acumulación de toxinas paralizantes de molusco (PSP) en las muestras de jurel (Trachurus trachurus) durante una proliferación do dinoflagelado Gymnodinium catenatum. Los altos niveles de toxinas PSP, alcanzando un valor máximo de 4800 μg STXeq kg–1, se determinaron en el pico de la proliferación (5.0 103 células l–1). El perfil de toxinas se examinó y se reveló que los compuestos dcSTX y B1 constintuían casi 90% de las toxinas (en base molar) encontrados en las muestras de jurel. Este perfil difiere claramente del perfil de toxinas conocido en cepas de G. catenatum aisladas de la costa portuguesa, que está dominado por toxinas N-sulfocarbamoyl, en particular las toxinas C1+2. Este trabajo muestra la prevalencia de dcSTX el ambiente pelágico y la transferencia de este compuesto a través de la cadena alimentaria. El jurel se identifica como un potencial vector de las toxinas PSP a lo largo de la costa portuguesa. Esta especie de pez tiene una posición central en la cadena alimentaria marina, siendo un importante depredador de zooplancton y, al mismo tiempo un elemento importante de la dieta de los depredadores superiores. Este estudio contribuye con valores ecológicos relevantes para evaluar los potenciales impactos de las proliferaciones de dinoflagelados productores de PST en los ecosistemas marinos o sus componentes, como los peces.

Descargas

Los datos de descargas todavía no están disponibles.

Citas

Bakke M.J., Horsberg T.E. 2010. Kinetic properties of saxitoxin in Atlantic salmon (Salmo salar) and Atlantic cod (Gadus morhua). Comp. Biochem. Phys. C 152: 444-450.

Cabral H.N., Murta A. 2002. The diet of blue whiting, hake, horse mackerel and mackerel off Portugal. J. Appl. Ichthyol. 18: 14-23. http://dx.doi.org/10.1046/j.1439-0426.2002.00297.x

Castonguay M., Levasseur M., Beaulieu J-L., Grégoire F., Michaud S., Bonneau E., Bates S.S. 1997. Accumulation of PSP toxins in Atlantic mackerel: seasonal and ontogenic variations. J. Fish. Biol. 50: 1203-1213. http://dx.doi.org/10.1111/j.1095-8649.1997.tb01648.x

Costa P.R., Botelho M.J., Lefebvre K.A. 2010. Characterization of paralytic shellfish toxins in seawater and sardines (Sardina pilchardus) during blooms of Gymnodinium catenatum. Hydrobiologia 655: 89-97. http://dx.doi.org/10.1007/s10750-010-0406-5

Costa P.R., Lage S., Barata M., Pousão-Ferreira P. 2011. Uptake, transformation, and elimination kinetics of paralytic shellfish toxins in white seabream (Diplodus sargus). Mar. Biol. 158: 2805-2811. http://dx.doi.org/10.1007/s00227-011-1779-3

Costa P.R., Pereira P., Guilherme S., Barata M., Nicolau L., Santos M.A., Pacheco M., Pousão-Ferreira P. 2012. Biotransformation modulation and genotoxicity in white seabream upon exposure to paralytic shellfish toxins produced by Gymnodinium catenatum. Aquat. Toxicol. 106: 42-47. http://dx.doi.org/10.1016/j.aquatox.2011.08.023 PMid:22057254

Ebert D.A. 1991. Diet of the seven gill shark Notorynchus cepedianus in the temperate coastal waters of southern Africa. S. Afr. J. Mar. Sci. 11: 565-572. http://dx.doi.org/10.2989/025776191784287547

EFSA (European Food Safety Authority) 2009. Scientific opinion of the panel on contaminants in the food chain on a request from the European Commission on Marine biotoxins in shellfish -Saxitoxin group. The EFSA Journal 1019: 1-76.

Fire S., Pruden J., Couture D., Wang Z., Bottein M-Y.D., Haynes B.L., Knott T., Bouchard D., Lichtenwalner A., Wippelhauser G. (in press). Saxitoxin exposure in endangered fish stocks: association of a shortnose sturgeon Acipenser brevirostrum mortality event with a harmful algal bloom in Maine. Mar. Ecol. Progr. Ser.

Geraci J.R., Anderson D.M., Timperi R.J., St Aubin D.J., Early G.A., Prescott J.H., Mayo C.A. 1989. Humpback whales (Megaptera novaeangliae) fatally poisoned by dinoflagellate toxin. Can. J. Fisher. Aquat. Sci. 46: 1895-1898. http://dx.doi.org/10.1139/f89-238

Hall S., Stricharz, G., Moczydlowski, E., Ravindran, A., Reichardt, P.B. 1990. The saxitoxins: sources, chemistry and pharmacology. In: Hall S., Stricharz G. (eds), Marine Toxins: Origin, Structure and Molecular Pharmacology. vol. 418. American Chemical Society Symposium Series, Washington, DC, pp. 29-65.

Hallegraeff G.M. 1993. A review of harmful algal blooms and their apparent global increase. Phycologia 32: 79-99. http://dx.doi.org/10.2216/i0031-8884-32-2-79.1

Hasle G.R. 1978. Phytoplankton manual: the inverted microscope method. In: Sournia, A. (ed.), Monographs on Oceanic Methodology. Unesco, Paris, pp. 88-96.

Jester R.J., Baugh K.A., Lefebvre K.A. 2009. Presence of Alexandrium catenella and paralytic shellfish toxins in finfish, shellfish and rock crabs in Monterey Bay, California, USA. Mar. Biol. 156: 493-504. http://dx.doi.org/10.1007/s00227-008-1103-z

Kwong R.W.M., Wang W.X., Lam P.K.S., Yu P.K.N. 2006. The uptake, distribution and elimination of paralytic shellfish toxins in mussels and fish exposed to toxic dinoflagellates. Aquat. Toxicol. 80: 82-91. http://dx.doi.org/10.1016/j.aquatox.2006.07.016 PMid:16959334

Lagos N., Andrinolo D. 2000. Paralytic Shellfish Poisoning (PSP): Toxicology and Kinetics. In: Botana L.M. (ed.), Seafood and Freshwater Toxins: Mode of Action, Pharmacology and Physiology. New York, Marcel Dekker, Inc. pp. 203-215 http://dx.doi.org/10.1201/9780203909539.ch10

Landsberg J.H. 2002. The effects of harmful algal blooms on aquatic organisms. Rev. Fisher. Sci. 10: 113-390. http://dx.doi.org/10.1080/20026491051695

Lawrence J.F., Niedzwiadek B. 2001. Quantitative determination of paralytic shellfish poisoning toxins in shellfish by using prechromatographic oxidation and liquid chromatography with fluorescence detection. J. AOAC Int. 84: 1099-1108. PMid:11501910

Lefebvre K.A., Elder N.E., Hershberger P.K., Trainer V.L., Stehr C.M., Scholz N.L. 2005. Dissolved saxitoxin causes transient inhibition of sensorimotor function in larval Pacific herring (Clupea harengus pallasi). Mar. Biol. 147: 1393-1402. http://dx.doi.org/10.1007/s00227-005-0048-8

Llewellyn L.E. 2006. Saxitoxin, a toxic marine natural product that targets a multitude of receptors. Nat. Prod. Rep. 23: 200-222. http://dx.doi.org/10.1039/b501296c PMid:16572228

Masó M., Garcés E. 2006. Harmful microalgae blooms (HAB); problematic and conditions that induce them. Mar. Pollut. Bull. 53: 620-630. http://dx.doi.org/10.1016/j.marpolbul.2006.08.006 PMid:17010385

Monteiro A., Costa P.R. 2011. Distribution and selective elimination of paralytic shellfish toxins in different tissues of Octopus vulgaris. Harmful Algae 10: 732-737. http://dx.doi.org/10.1016/j.hal.2011.06.004

Mortensen A.M. 1985. Massive fish mortalities in the Faroe Islands caused by a Gonyaulax excavata red tide. In: Anderson D.A., White A.W., Baden D.G. (eds), Toxic Dinoflagellates. New York, pp. 165-170.

Negri A.P., Bolch C.J.S., Geier S., Green D.H., Park T.G., Blackburn S.I. 2007. Widespread presence of hydrophobic paralytic shellfish toxins in Gymnodinium catenatum. Harmful Algae 6: 774-780. http://dx.doi.org/10.1016/j.hal.2007.04.001

Oshima Y., Blackburn S.I., Hallegraeff G.M. 1993. Comparative study on paralytic shellfish toxin profiles of the dinoflagellate Gymnodinium catenatum from three different countries. Mar. Biol. 116. 471-476. http://dx.doi.org/10.1007/BF00350064

Reyero M., Cacho E., Martínez A., Vázquez J., Marina A., Fraga S., Franco J.M. 1999. Evidence of saxitoxin derivatives as causative agents in the 1997 mass mortality of monk seals in the Cape Blanc Peninsula. Nat. Toxins 7: 311-315. http://dx.doi.org/10.1002/1522-7189(199911/12)7:6<311::AID-NT75>3.0.CO;2-I

Robineau B., Gagné J.A., Fortier L., Cembella A.D. 1991. Potential impact of a toxic dinoflagellate (Alexandrium excavatum) bloom on survival of fish and crustacean larvae. Mar. Biol. 108: 293-301. http://dx.doi.org/10.1007/BF01344344

Samson J.C., Shumway S.E., Weis J.S. 2008. Effects of the toxic dinoflagellate, Alexandrium fundyense on three species of larval fish: a food-chain approach. J. Fish Biol. 72: 168-188. http://dx.doi.org/10.1111/j.1095-8649.2007.01698.x

Sephton D.H, Haya K., Martin J.L., Legresley M.M., Page F.H. 2007. Paralytic shellfish toxins in zooplankton, mussels, lobsters and caged atlantic salmon, Salmo salar, during a bloom of Alexandrium fundyense of Grand Manan Island, in the Bay of Fundy. Harmful Algae 5: 745-758. http://dx.doi.org/10.1016/j.hal.2007.03.002

Silva M.A. 1999. Diet of dolphins, Delphinus delphis, off the Portuguese continental coast. J. Mar. Biol. Assoc. U.K. 79: 531-540. http://dx.doi.org/10.1017/S0025315498000654

Silva S., Larsen J., Rangel I., Jonico V. 2011. Fish mortality associated with Alexandrium cf. fundyense in Lobito Bay, Angola. Harmful Algae News 44: 5-5

Vale C., Alfonso A., Vieytes M.R., Romarís X.M., Arévalo F., Botana A.M., Botana L.M. 2008. In vitro and in vivo evaluation of paralytic shellfish poisoning toxin potency and the influence of the pH of extraction. Anal. Chem. 80: 1770-1776. http://dx.doi.org/10.1021/ac7022266 PMid:18232710

White A.W. 1977. Dinoflagellate toxins as probable cause of an Atlantic herring (Clupea harengus harengus) kill, and pteropods as apparent vector. J. Fish. Res. Bd. Can. 34: 2421- 2424. http://dx.doi.org/10.1139/f77-328

White A.W., 1981. Sensitivity of marine fishes to toxins from the red-tide dinoflagellate Gonyaulax excavata and implications for fish kills. Mar. Biol. 65: 255-260. http://dx.doi.org/10.1007/BF00397119

Wiese M., D'Agostino P.M., Mihali T.K., Moffitt M.C., Neilan B.A. 2010. Neurotoxic alkaloids: saxitoxin and its analogs. Mar. Drugs 8: 2185-2211. http://dx.doi.org/10.3390/md8072185 PMid:20714432 PMCid:2920551

Descargas

Publicado

2013-03-30

Cómo citar

1.
Lage S, Reis Costa P. Determinación de toxinas paralizantes en el jurel (Trachurus trachurus) durante una proliferación de Gymnodinium catenatum: la prevalencia de decarbamoilsaxitoxina en la red trófica marina. Sci. mar. [Internet]. 30 de marzo de 2013 [citado 22 de febrero de 2025];77(1):13-7. Disponible en: https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1437

Número

Sección

Artículos