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Acta Parasitologica


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Volume 59, Issue 1

Issues

Anisakids of seals found on the southern coast of Baltic Sea

Michał Skrzypczak
  • Department of Invertebrate Zoology and Parasitology, Laboratory of Parasitology and General Zoology, University of Gdansk, Faculty of Biology, Wita Stwosza 59, 80-308, Gdańsk, Poland
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/ Jerzy Rokicki
  • Department of Invertebrate Zoology and Parasitology, Laboratory of Parasitology and General Zoology, University of Gdansk, Faculty of Biology, Wita Stwosza 59, 80-308, Gdańsk, Poland
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/ Iwona Pawliczka / Katarzyna Najda
  • Department of Invertebrate Zoology and Parasitology, Laboratory of Parasitology and General Zoology, University of Gdansk, Faculty of Biology, Wita Stwosza 59, 80-308, Gdańsk, Poland
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/ Joanna Dzido
  • Department of Invertebrate Zoology and Parasitology, Laboratory of Parasitology and General Zoology, University of Gdansk, Faculty of Biology, Wita Stwosza 59, 80-308, Gdańsk, Poland
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Published Online: 2014-02-26 | DOI: https://doi.org/10.2478/s11686-014-0226-2

Abstract

In the present study 5 grey seals (Halichoerus grypus), 3 common seals (Phoca vitulina) and 1 ringed seal (Pusa hispida) bycaught or stranded on the Polish Baltic Sea coast in years 2000-2006 were investigated for the infestation of parasitic anisakid nematodes. 749 of anisakids were found. The most common were: Contracaecum osculatum (59.3%) and Pseudoterranova decipiens (31.0%). There were also small numbers of Anisakis simplex (0.8%). After performing RFLP three sibling species were found. C. osculatum was identified as C. osculatum C, P decipiens was identified as P. decipiens sensu stricto and A. simplex — A. simplex sensu stricto. Nematodes found in seals were mostly in L4 and adult life stage — both of them were equal with some minor variations among the specimens. Sex ratio was also equal, but there was slight excess of males in some cases. There was a minority of L3 larvae belonging to A. simplex species (0.8%).

Keywords: Anisakid nematodes; seal; Baltic Sea

  • [1] Anderson R.C. 2000. Nematode parasites of vertebrates, their development and transmission. CABI, Wallingford, 650 pp. http://dx.doi.org/10.1079/9780851994215.0000Google Scholar

  • [2] Aspholm E.P., Ugland K.I., Jødestøl K.A., Berland B. 1995. Sealworm (Pseudoterranova decipiens) infection in common seals (Phoca vitulina) and potential intermediate fish hosts from outer Oslofjord. International Journal for Parasitology, 25, 367–373. DOI: 10.1016/0020-7519(94)00133-9. http://dx.doi.org/10.1016/0020-7519(94)00133-9CrossrefGoogle Scholar

  • [3] Berland B. 2005. Whole Mounts. KUSTEM, Terengganu, 53 pp. Google Scholar

  • [4] D’Amelio S., Mathiopoulos K.D., Santos C.P., Pugachev O.N., Webb S.C., Picanço M., Paggi L. 2000. Genetic markers in ribosomal DNA for the identification of members of the genus Anisakis (Nematoda: Ascaridoidea) defined by polymerase chain reaction-based restriction fragment length polymorphism. International Journal for Parasitology, 30, 223–226. http://dx.doi.org/10.1016/S0020-7519(99)00178-2Google Scholar

  • [5] Grabda-Kazubska B., Okulewicz A. 2005. Pasożyty ryb Polski (klucze do oznaczania) — Nicienie (Nematoda). Polskie Towarzystwo Parazytologiczne, Warszawa, 169 pp. Google Scholar

  • [6] Guz L., Studzińska M.B., Sadzikowski A.B., GundŁach J.L. 2005. Anisakioza. Annales Universitatis Mariae Curie-Skłodowska, LX(10), 74–83. Google Scholar

  • [7] Harding K.C., Härkönen T., Helander B., Karlsson O. 2007. Status of Baltic grey seals: Population assessment and extinction risk. NAMMCO Scientific Publications, 6, 33–56. Google Scholar

  • [8] Kijewska A., Rokicki J., Sitko J., Węgrzyn G. 2002. Ascaridoidea: a simple DNA assay for identification of 11 species infecting marine and freshwater fish, mammals, and fish-eating birds. Experimental Parasitology, 101, 35–39. DOI: 10.1016/S0014-4894(02)00031-0. http://dx.doi.org/10.1016/S0014-4894(02)00031-0CrossrefGoogle Scholar

  • [9] Klimpel S., Palm H.W., Rückert S., Piątkowski U. 2004. The life cycle of Anisakis simplex in the Norwegian Deep (northern North Sea). Parasitology Research, 94, 1–9. http://dx.doi.org/10.1007/s00436-004-1154-0Google Scholar

  • [10] Klimpel S., Palm H.W. 2011. Anisakid nematode (Ascaridoidea) life cycles and distribution: increasing zoonotic potential in the time of climate change? In: (Ed. H. Mehlhorn) Parasitology Research Monographs, Vol. 2. Heidelberg, 201–222. DOI: 10.1007/s00436-004-1154-0. CrossrefGoogle Scholar

  • [11] Køie M., Berland B., Burt M.D.B. 1995. Development to thirdstage larvae occurs in the eggs of Anisakis simplex and Pseudoterranova decipiens (Nematoda, Ascaridoidea, Anisakidae). Canadian Journal of Fisheries and Aquatic Sciences, 52, 134–139. DOI: 10.1186/1756-3305-1-23. http://dx.doi.org/10.1139/f95-519CrossrefGoogle Scholar

  • [12] Køie M., Fagerholm H.P. 1995. The life cycle of Contracaecum osculatum (Rudolphi, 1802) sensu stricto (Nematoda, Ascaridoidea, Anisakidae) in view of experimental infections. Parasitology Research, 81, 481–489. DOI: 10.1007/BF00931790. http://dx.doi.org/10.1007/BF00931790CrossrefGoogle Scholar

  • [13] La Rosa G., D’Amelio S., Pozio E. 2005. Molecular identification of nematode worms from seafood (Anisakis spp. and Pseudoterranova spp.) and meat (Trichinella spp.). Methods in Biotechnology, 21, 217–232. DOI: 10.1385/1-59259-990-7:217. http://dx.doi.org/10.1385/1-59259-990-7:217CrossrefGoogle Scholar

  • [14] Lehnert K., Raga J.A., Siebert U. 2007. Parasites in harbour seals (Phoca vitulina) from the German Wadden Sea between two phocine distemper virus epidemics. Helgoland Marine Research, 61, 239–245. DOI: 10.1007/s10152-007-0072-9. http://dx.doi.org/10.1007/s10152-007-0072-9Web of ScienceCrossrefGoogle Scholar

  • [15] Liskins N. 2002. Dissection results of dead seals perished in fishing gear in the Gulf of Riga. Acta Zoologica Lituanica, 12, 369–371. DOI: 10.1080/13921657.2002.10512526. http://dx.doi.org/10.1080/13921657.2002.10512526CrossrefGoogle Scholar

  • [16] Lundström K., Hjerne O., Lunneryd S-G., Karlsson, O. 2010. Understanding the diet composition of marine mammals: grey seals (Halichoerus grypus) in the Baltic Sea. ICES Journal of Marine Science, 67, 1230–1239. DOI: 10.1093/icesjms/fsq022 http://dx.doi.org/10.1093/icesjms/fsq022Web of ScienceCrossrefGoogle Scholar

  • [17] Martell D.J., McClelland G. 1995. Transmission of Pseudoterranova decipiens (Nematoda: Ascaridoidea) via benthic macrofauna to sympatric flatfishes (Hippoglossoides platessoides, Pleuronectes ferrugineus, P. americanus) on Sable Island Bank, Canada. Marine Biology, 122, 129–135. DOI: 10.1007/BF00349286. http://dx.doi.org/10.1007/BF00349286CrossrefGoogle Scholar

  • [18] Mattiucci S., Nascetti G. 2007. Genetic diversity and infection levels of anisakid nematodes parasitic in fish and marine mammals from Boreal and Austral hemispheres. Veterinary Parasitology, 148, 43–57. DOI: 10.1016/j.vetpar.2007.05.009. http://dx.doi.org/10.1016/j.vetpar.2007.05.009CrossrefWeb of ScienceGoogle Scholar

  • [19] Mattiucci S., Paoletti M., Damiano S., Nascetti G. 2007. Molecular detection of sibling species in anisakid nematodes. Parassitologia, 49, 147–153. Google Scholar

  • [20] Myjak P., Szostakowska B., Wojciechowski J., Pietkiewicz H., Rokicki J. 1994. Anisakid larvae in cod from the southern Baltic Sea. Archive of Fishery and Marine Research, 42, 149–161. Google Scholar

  • [21] McClelland G. 2002. The trouble with sealworms (Pseudoterranova decipiens species complex, Nematoda): a review. Parasitology, 124, 183–203. DOI: 10.1017/S0031182002001658. http://dx.doi.org/10.1017/S0031182002001658CrossrefGoogle Scholar

  • [22] Ólafsdóttir D., Hauksson E. 1997. Anisakid (Nematoda) infestations in Icelandic grey seals (Halichoerus grypus Fabr.). Journal of Northwest Atlantic Fishery Science, 22, 259–269. DOI: 10.1155/2011/235832. http://dx.doi.org/10.2960/J.v22.a19CrossrefGoogle Scholar

  • [23] Paggi L., Mattiucci S., Gibson D.I., Berland B., Nascetti G., Cianchi R., Bullini L. 2000. Pseudoterranova decipiens species A and B (Nematoda, Ascaridoidea): nomenclatural designation, morphological diagnostic characters and genetic markers. Systematic Parasitology, 45, 185–197. DOI: 10.1023/A: 1006296316222. http://dx.doi.org/10.1023/A:1006296316222CrossrefGoogle Scholar

  • [24] Rokicki J. 2006. Anisakidoza (anizakidoza, anisakiasis). In: (Ed. A. KotŁowski), Medycyna i higiena tropikalna. Akademia Medyczna w Gdańsku, Gdynia, 488–507. Google Scholar

  • [25] Rokicki J., Rolbiecki L., Skóra A. 2009. Helminth parasites of twaite shad, Alosa fallax (Actinopterygii: Clupeiformes: Clupeidae) from the southern Baltic Sea. Acta Ichthyologica et Piscatoria, 39, 7–10. http://dx.doi.org/10.3750/AIP2009.39.1.02Web of ScienceGoogle Scholar

  • [26] Sinisalo T. 2007. Diet and foraging of ringed seals in relation to helminth parasite asemblages. Jyväskylä University Printing House, Jyväskylä, 41 pp. Google Scholar

  • [27] Sobecka E., Łuczak E., Więcaszek B., Antoszek A. 2011. Parasite community structure of cod from Bear Island (Barents Sea) and Pomeranian Bay (Baltic Sea). Polish Polar Research, 32, 253–262. DOI: 10.2478/v10183-011-0016-6. http://dx.doi.org/10.2478/v10183-011-0016-6CrossrefWeb of ScienceGoogle Scholar

  • [28] Szostakowska B., Myjak B., Wyszyński M., Piętkiewicz H., Rokicki J. 2005. Prevalence of anisakin nematodes in fish from southern Baltic Sea. Polish Journal of Microbiology, 54, 41–45. Google Scholar

  • [29] Valtonen E. T., Fagerholm H.P., Helle E. 1988. Contracaecum osculatum (Nematoda: Anisakidae) in fish and seals in Bothnian Bay (northeastern Baltic Sea). International Journal for Parasitology, 18, 365–370. DOI: 10.1186/1756-3305-1-23 http://dx.doi.org/10.1016/0020-7519(88)90146-4CrossrefGoogle Scholar

  • [30] Weerasooriya M. V., Fujipo T., Ishii Y., Kagei N. 1986. The value of external morphology in the identification of larval anisakid nematodes: a scanning electron microscope study. Parasitenkunde, 72, 765–778. DOI: 10.1007/BF00925097 http://dx.doi.org/10.1007/BF00925097CrossrefGoogle Scholar

  • [31] Zhu X. Q., D’Amelio S., Palm H. W., Paggi L., George-Nascimento M., Gasser R.B. 2002. SSCP-based identifications of mem bers within the Pseudoterranova decipiens complex (Nematoda: Ascaridoidea: Anisakidae) using genetic markers in the internal transcribed spacers of ribosomal DNA. Parasitology, 124, 615–623. DOI: 10.1017/S0031182002001579 http://dx.doi.org/10.1017/S0031182002001579CrossrefGoogle Scholar

About the article

Published Online: 2014-02-26

Published in Print: 2014-03-01


Citation Information: Acta Parasitologica, Volume 59, Issue 1, Pages 165–172, ISSN (Online) 1896-1851, DOI: https://doi.org/10.2478/s11686-014-0226-2.

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© 2014 W. Stefański Institute of Parasitology, PAS. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License. BY-NC-ND 3.0

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