한국임상수의학회지 (Journal of Veterinary Clinics)

  • 제27권1호
  • /
  • Pages.11-16
  • /
  • 2010
  • /
  • 1598-298X(pISSN)
  • /
  • 2384-0749(eISSN)
한국임상수의학회 (The Korean Society of Veterinary Clinics)
권호 표지

페리칸에서 분리한 Contracaecum rudolphii (Nematoda: Anisakidae)의 형태학적 연구

Morphological Study of Contracaecum rudolphii (Nematoda: Anisakidae) from White Pelican

  • 김현철 (강원대학교 수의과대학) ;
  • 김남수 (충남대학교 수의과대학) ;
  • 손화영 (충남대학교 수의과대학) ;
  • 권보근 (충남대학교 수의과대학) ;
  • 허진 (전북대학교 수의과대학) ;
  • 조정곤 (전북대학교 수의과대학) ;
  • 박배근 (충남대학교 수의과대학)
  • Kim, Hyeon-Cheol (College of Veterinary Medicine, Kangwon National University) ;
  • Kim, Nam-Soo (Research Institute of Veterinary Science, College of Veterinary Medicine, Chungnam National University) ;
  • Son, Hwa-Young (Research Institute of Veterinary Science, College of Veterinary Medicine, Chungnam National University) ;
  • Kwon, Bo-Keun (Research Institute of Veterinary Science, College of Veterinary Medicine, Chungnam National University) ;
  • Hur, Jin (College of Veterinary Medicine and Bio-Safety Research Institute, Chonbuk National University) ;
  • Cho, Jeong-Gon (College of Veterinary Medicine and Bio-Safety Research Institute, Chonbuk National University) ;
  • Park, Bae-Keun (Research Institute of Veterinary Science, College of Veterinary Medicine, Chungnam National University)
  • 발행 : 2010.02.28
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

대전동물원에 탄자니아로부터 페리칸이 수입되었고 5일 후에 한 마리가 폐사 하였다. 선위에서 다수의 기생충을 분리하였으며 다음과 같은 특징을 가지고 있었다. 3개의 입술이 존재하였고 입술에는 치상돌기가 존재하지 않았으며 입술 사이에는 순간돌기가 잘 발달되어 있었다. 순간돌기는 삼각형으로 분기되어 있지 않았다. 수컷은 다수의 전항문 유두 (69-79)가 아복면에 배열되어 있었다. 부총배설강 유두는 대형의 1쌍과 5개가 존재하였다. 이러한 형태학적 특징을 기초로 페리칸에서 분리한 기생충을 Contracaecum rudolphii로 분류하였다.

A white pelican, Pelecanus onccrotalus, was imported from Tanzania and died 5 days later in Daejeon zoo in Korea. The proventriculus of bird was found to contain parasites. The taxonomic status of the nematodes was studied by morphological and morphometric analysis using light and scanning electron microscopy. Only one species Contracaecum occurred in the proventriculus with high values of infection. Morphological characters of the parasite were as follows: The worms have three lips without cuticular dentigerous ridges, and well developed interlabia. The interlabia have a triangular shape, non-bifurcated. Males possess numerous preanal papillae (69-79 pairs) arranged in single subventral rows. Paracloacal papillae were separated 5 postanal papillae and 1 larger pairs. All the characters of the above studied specimens are very similar to those of C. rudolphii complex. Accordingly, the parasites from white pelican were identified belong to the C. rudolphii complex.

키워드

참고문헌

  1. Abollo E, Gestal C, Pascual S. Anisakid infection in the European shag Phalacrocorax aristotelis aristotelis. J Helminthol 2001; 75: 209-214.
  2. Barson M. The occurrence of Contracaecum sp. larvae (Nematoda: Anisakidae) in the catfish Clarias gariepinus (Burchell) from lake Chivero, Zimbabwe. Onderstepoort J Vet Res 2004; 71: 35-39.
  3. Barus V, Sergeeva TP, Sonin MD, Ryzhikov KM. Helminths of fish-eating birds of the palearctic Region I. Academia, Publishing House of the Czechoslovak Academy of Science, Prague. 1978.
  4. Cianchi R, Orecchia P, Berland B, Paggi L, D'Amelio S, Mattiucci S, Nascetti G, Bullini L. Genetic studies on some Contracaecum species, parasites of fish-eating birds. Abstract of 6th European Multicolloquium of Parasitology, The Hague, The Netherlands. 1992; 127.
  5. D'Amelio S, Nascetti G, Mattiucci S, Cianchi R, Orecchia P, Paggi L, Berland B, Bullini L. Ricerche electroforetiche su alcune specie del genere Contracaecum, parassiti di uccelli ittiofagi (Ascaridida: Anisakidae). Parassitologia 1990; 32 (suppl. 1): 77.
  6. D'Amelio S, Mattiucci S, Nascetti G, Orecchia P, Paggi L, Bullini L. Contracaecum rudolphii s.l. in pesci de uccelli ittiofagi del laghi del Paeco Nazionale del Circeo. 1991; Oebalia (suppl. 17): 569-570.
  7. Deardorff TL, Overstreet RM. Contracaecum multipapillatum (= C. robustum) from fishes and birds in the northern Gulf of Mexico. J Parasitol 1980; 66: 853-856. https://doi.org/10.2307/3280688
  8. Dyer WG, Williams Jr EH, Mignucci-Giannom AA, Jimenez- Marrero NM, Bunkley-Williams L, Moore DP, Pence DB. Helminth and arthropod parasites of the brown pelican, Pelecanus occidentalis, in Puerto Rico, with a compilation of all metazoan parasites reported from this host in the Western Hemisphere. Avian Pathol 2002; 21: 441-448.
  9. Fagerholm HP. Patterns of caudal papillae in Contracacum osculatum (Nematoda) and some related species from different regions of the world. Int J Parasitol 1988; 18: 1039-1051. https://doi.org/10.1016/0020-7519(88)90074-4
  10. Fagerholm HP. Intraspecific variability of the morphology in a single population of the seal parasite Contracaecum osculatum (Nematoda, Ascaridoidea), with a redescription of the species. Zool Scripta 1989; 18: 33-41. https://doi.org/10.1111/j.1463-6409.1989.tb00121.x
  11. Fagerholm HP. Systematic implications of male caudal morphology in ascaridoid nematode parasites. System Parasitol 1991; 19: 215-228. https://doi.org/10.1007/BF00011888
  12. Fagerholm HP. Gibson DI. A redescription of the pinniped parasite Contracaecum ogmorhini (Nematoda, Ascaridoidea), with an assessment of its antibioreal circumpolar distribution. Zool Scr 1987; 16: 19-24. https://doi.org/10.1111/j.1463-6409.1987.tb00047.x
  13. Fagerholm HP, Overstreet RM, Humphrey-smith I. Contracaecum magnipapillatum (Nematoda, Ascaridoidea): resurrection and pathogenic effect of a common parasite from the proventriculus of Anous minutus from the Great Barrier Reef, with a note on C. variegatum. Helminthologia 1996; 33: 195-207.
  14. Hartwich G. CIH keys to the Nematodes Parasites of Vertebrates. 2. Keys to genera of the Ascaridoidae. Commonwealth Agricultural Bureaux, England. 1974; 15.
  15. Hugot JP, Morand S, Vassart M. Morphological study of Contracaecum magnicollare (Nematoda, Anisakidae) from Anous minutus (Aves, Laridae). System Parasitol 1991; 20: 229-236. https://doi.org/10.1007/BF00009787
  16. Huizinga, HW. Studies on the life cycle and histopathology of the nematode parasite Contracaecum spiculigerum in fish-eating birds. Northeast Fish Wildlife Conf. Harrisburg, Pennsylvania, Ja. 1965; 17.
  17. Ito M, Sato T, Shirai W, Kikuchi S. Parasites and related pathological lesions in the gastrointestinal tract of a seal (Phoka vitulina Linnaeus). J Vet Med Sci 1998; 60: 1025-1028. https://doi.org/10.1292/jvms.60.1025
  18. Kijewska A, Rokicki J, Sitko J, Wegryzyn G. Ascaridoidea: a simple DNA assay for identification of 11 species infecting marine and freshwater fish, mammals, and fish-eating birds. Exp Parasitol 2002; 101: 35-39. https://doi.org/10.1016/S0014-4894(02)00031-0
  19. Kloser H, Plotz J. Morphological distinction between adult Contracaecum radiatum and Contracaecum osculatum (Nematoda, Anisakidae) from the weddell seal (Leptonychotes weddelli). Zool Scr 1992; 21: 129-132. https://doi.org/10.1111/j.1463-6409.1992.tb00315.x
  20. Liu SK. and Edward AG. Gastric ulcers associated with Contracaecum spp.(Nematod: Ascaroidea) in a steller sea lion and a white pelican. J Wild Dis 1971; 7: 266-271.
  21. Lymbery AJ, Doupe RG, Munshi MA, Wong T. Larvae of Contracaecum sp. among inshore fish species of southwestern Australia. Dis Aquat Org 2002; 51: 157-159. https://doi.org/10.3354/dao051157
  22. Martins, ML., Onaka, EM., Fenerick, J. Larval Contracaecum sp. (Nematoda: Anisakidae) in Hoplias malabaricus and Hoplerythrinus unitaeniatus (Osteichthyes: Erythrinidae) of economic importance in occidental marshlands of Maranhao, Brazil. Vet Parasitol 2005; 127: 51-59. https://doi.org/10.1016/j.vetpar.2004.09.026
  23. Mattiucci S, Cianchi R, Nascetti G, paggi L, Sardella N, Timi J, Webb SC, Bastida R, Rodriguez D, Bullini L. Genetic evidence for two sibling species within Contracaecum ogmorhini Johnston & Mawson, 1941 (Nematoda: Anisakidae) from otariid seals boreal and austral regions. System Parasitol 2003; 54: 13-23. https://doi.org/10.1023/A:1022145926409
  24. Mattiucci S, Nascetti G, Dailey M, Webb SC, Barros NB, Cianchi R, Bullini L. Evidence for a new species of Anisakis Dujardin, 1845: morphological description and genetic relationships between congeners (Nematoda: Anisakidae). System Parasitol 2005; 61: 157-171. https://doi.org/10.1007/s11230-005-3158-2
  25. McCarthy J, Moore TA. Emerging helminth zoonoses. Int J Parasitol 2000; 30: 1351-1360. https://doi.org/10.1016/S0020-7519(00)00122-3
  26. Sakanari JA, McKerrow JH. Anisakiasis. Clin Microbiol Rev 1989; 278-284.
  27. Szostakowska B, Myjak P, Kur J. Identification of anisakid nematodes from the southern Baltic Sea using PCR-based methods. Mol Cell Probes 2002; 16: 111-118. https://doi.org/10.1006/mcpr.2001.0391
  28. Yamaguti, S. Systema helminthum, I, II. Interscience Publishers, New York. 1961
  29. Yang TB, Miao SY, Liao XH, Wang ZJ. Studies on the dynamic mechanism of cavity helminthes in Gymnocypris przewalskii przewalskii in the Qinghai Lake: ecological approach and their relationship to feeding of host. Acta Hydrobiol Sinica 2001; 25: 268-273.