DOI QR코드

DOI QR Code

Anisakis pegreffii Larvae in Sea Eels (Astroconger myriaster) from the South Sea, Republic of Korea

  • Cho, Jaeeun (Department of Parasitology and Tropical Medicine, Seoul National University College of Medicine) ;
  • Lim, Hyemi (Department of Parasitology and Tropical Medicine, Seoul National University College of Medicine) ;
  • Jung, Bong-Kwang (Department of Parasitology and Tropical Medicine, Seoul National University College of Medicine) ;
  • Shin, Eun-Hee (Department of Parasitology and Tropical Medicine, Seoul National University College of Medicine) ;
  • Chai, Jong-Yil (Department of Parasitology and Tropical Medicine, Seoul National University College of Medicine)
  • Received : 2015.03.03
  • Accepted : 2015.04.24
  • Published : 2015.06.30

Abstract

Anisakis simplex sensu stricto (s.s.), Anisakis pegreffii, Anisakis berlandi (=A. simplex sp. C), and Anisakis typica are the 4 major species of Anisakis type I larvae. In the Republic of Korea (Korea), A. pegreffii, A. berlandi, and A. typica larvae in fish hosts has seldom been documented. In this study, molecular analysis was performed on Anisakis larvae from the sea eels (Astroconger myriaster), the major source of human anisakiasis in Korea, collected from Tongyeong City, a southern coastal area of Korea. All 20 sea eels examined were infected with Anisakis type I larvae (160 larvae; 8 per fish). Their species were analyzed using PCR-RFLP patterns and nucleotide sequences of internal transcribed spacers (ITS1, 5.8 subunit gene, and ITS2) and mitochondrial cytochrome c oxidase 2 (cox2). Most (86.8%; 112/129) of the Anisakis type I larvae were A. pegreffii, and 7.8% (10/129) were A. typica. The remaining 5.4% (7/129) was not identified. Thus, A. pegreffii is the major species of anisakid larvae in sea eels of the southern coast of Korea.

Keywords

References

  1. Sohn WM, Chai JY. Anisakiosis (Anisakidosis). In Palmer SR, Soulsby L, Torgerson PR, Brown WG, eds, Oxford Textbook of Zoonoses. 2nd ed. Oxford, UK. Oxford University Press. 2011. pp 774-786.
  2. Chai JY, Murrell KD, Lymbery AJ. Fish-borne parasitic zoonoses: status and issues. Int J Parasitol 2005; 35: 1233-1254. https://doi.org/10.1016/j.ijpara.2005.07.013
  3. D’Amelio S, Mathiopoulos KD, Brandonisio O, Lucarelli G, Doron zo F, Paggi L. Diagnosis of a case of gastric anisakidosis by PCR-based restriction fragment length polymorphism analysis. Parassitologia 1999; 41: 591-593.
  4. Fumarola L, Monno R, Ierardi E, Rizzo G, Giannelli G, Lalle M, Pozio E. Anisakis pegreffii etiological agent of gastric infections in two Italian women. Foodborne Pathog Dis 2009; 6: 1157-1159. https://doi.org/10.1089/fpd.2009.0325
  5. Mattiucci S, Paoletti M, Borrini F, Palumbo M, Palmieri RM, Gomes V, Casati A, Nascetti G. First molecular identification of the zoonotic parasite Anisakis pegreffii (Nematoda: Anisakidae) in a paraffin-embedded granuloma taken from a case of human intestinal anisakiasis in Italy. BMC Infect Dis 2011; 11: 82 (1-6). https://doi.org/10.1186/1471-2334-11-82
  6. Mattiucci S, Fazii P, Rosa AD, Paoletti M, Megna AS, Glielmo A, de Angelis M, Costa A, Meucci C, Calvaruso V, Sorrentini I, Palma G, Bruschi F, Nascetti G. Anisakiasis and gastroallergic reactions associated with Anisakis pegreffii infection, Italy. Emerg Infect Dis 2013; 19: 496-499. https://doi.org/10.3201/eid1903.121017
  7. Umehara A, Kawakami Y, Araki J, Uchida A. Molecular identification of the etiological agent of the human anisakiasis in Japan. Parasitol Int 2007; 56: 211-215. https://doi.org/10.1016/j.parint.2007.02.005
  8. Arizono N, Yamada M, Tegoshi T, Yoshikawa M. Anisakis simplex sensu stricto and Anisakis pegreffii: biological characteristics and pathogenetic potential in human anisakiasis. Foodborne Pathog Dis 2012; 9: 517-521. https://doi.org/10.1089/fpd.2011.1076
  9. Lim H, Jung BK, Cho J, Yooyen T, Shin EH, Chai JY. Molecular diagnosis of cause of anisakiasis in humans, South Korea. Emerg Infect Dis 2015; 21: 342-344. https://doi.org/10.3201/eid2102.140798
  10. Chai JY, Cho SR, Kook J, Lee SH. Infection status of the sea eel (Astroconger myriaster) purchased from the Noryangjin fish market with anisakid larvae. Korean J Parasitol. 1992;30:157-162. https://doi.org/10.3347/kjp.1992.30.3.157
  11. Mattiucci S, Cipriani P, Webb SC, Paoletti M, Marcer F, Bellisario B, Gibson DI, Nascetti G. Genetic and morphological approaches distinguish the three sibling species of the Anisakis simplex species complex, with a species designation as Anisakis berlandi n. sp. for A. simplex sp. C (Nematoda: Anisakidae). J Parasitol 2014; 100: 199-214. https://doi.org/10.1645/12-120.1
  12. Chai JY, Cho YM, Sohn WM, Lee SH. Larval anisakids collected from the yellow corvine in Korea. Korean J Parasitol 1986; 24: 1-11.
  13. Kim KH, Joo KH, Rim HJ. A study about infection state of anisakis larvae and parasitic helminths in salmon (Onchorhynchus keta) and sea trout (Oncorhynchus masou) which were caught from Taepo Port, Kangwon Do. Korean J Rural Med 1990; 15: 27-32.
  14. Song SB, Hwang EG. Infection status of larval anisakids in Astroconger myriaster collected from the Southern Sea near Pusan. Korean J Parasitol 1992; 30: 263-267. https://doi.org/10.3347/kjp.1992.30.4.263
  15. Song SB, Lee SR, Chung HH, Han NS. Infection status of anisakid larvae in anchovies purchased from local fishery market near southern and eastern sea in Korea. Korean J Parasitol 1995; 33: 95-99 (in Korean). https://doi.org/10.3347/kjp.1995.33.2.95
  16. Choi SH, Kim J, Jo JO, Cho MK, Yu HS, Cha HJ, Ock MS. Anisakis simplex larvae: infection status in marine fish and cephalopods purchased from the Cooperative Fish Market in Busan, Korea. Korean J Parasitol 2011; 49: 39-44. https://doi.org/10.3347/kjp.2011.49.1.39
  17. Cho SH, Lee SE, Park OH, Na BK, Sohn WM. Larval anisakid infections in marine fish from three sea areas of the Republic of Korea. Korean J Parasitol 2012; 50: 295-299. https://doi.org/10.3347/kjp.2012.50.4.295
  18. Lee MH, Cheon DS, Choi C. Molecular genotyping of Anisakis species from Korean sea fish by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Food Control 2009; 20: 623-626. https://doi.org/10.1016/j.foodcont.2008.09.007
  19. Setyobudi E, Jeon CH, Lee CH, Seong KB and Kim JH. Occurrence and identification of Anisakis spp. (Nematoda: Anisakidae) isolated from chum salmon (Oncorhynchus keta) in Korea. Parasitol Res 2011; 108: 585-592. https://doi.org/10.1007/s00436-010-2101-x
  20. Sohn WM, Kang JM, Na BK. Molecular analysis of Anisakis type I larvae in marine fish from three different sea areas in Korea. Korean J Parasitol 2014; 52: 383-389. https://doi.org/10.3347/kjp.2014.52.4.383
  21. D'Amelio S, Mathiopoulos KD, Santos CP, Pugachev ON, Webb SC, Picanco M, Paggi L. 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. Int J Parasitol 2000; 30: 223-226. https://doi.org/10.1016/S0020-7519(99)00178-2
  22. Nadler SA, Hudspeth DSS. Phylogeny of the Ascaridoidea (Nematoda: Ascaridida) based on three genes and morphology: hypotheses of structural and sequence evolution. J Parasitol 2000; 86: 380-393. https://doi.org/10.1645/0022-3395(2000)086[0380:POTANA]2.0.CO;2
  23. Umehara A, Kawakami Y, Matsui T, Araki J, Uchida A. Molecular identification of Anisakis simplex sensu stricto and Anisakis pegreffii (Nematoda: Anisakidae) from fish and cetacean in Japanese waters. Parasitol Int 2006; 55: 267-271. https://doi.org/10.1016/j.parint.2006.07.001
  24. Campana-Rouget PY, Biocca E. Une Nouvelle Espece D'Anisakis Chez un Phoque Mediterranean. Ann de Parasitol 1955; 30: 477-480. https://doi.org/10.1051/parasite/1955305477
  25. Zhang L, Hu M, Shamsi S, Beveridge I, Li H, Xu Z, Li L, Cantacessi C, Gasser RB. The specific identification of anisakid larvae from fishes from the Yellow Sea, China, using mutation scanning-coupled sequence analysis of nuclear ribosomal DNA. Mol Cell Probes 2007; 21: 386-390. https://doi.org/10.1016/j.mcp.2007.05.004
  26. Nascetti G, Paggi L, Orecchia P, Smith JW, Mattiucci S, Bullini L. Electrophoretic studies on the Anisakis simplex complex (Ascaridida: Anisakidae) from the Mediterranean and North-East Atlantic. Int J Parasitol 1986; 16: 633-640. https://doi.org/10.1016/0020-7519(86)90032-9
  27. Quiazon KMA, Yoshinaga T, Ogawa K. Distribution of Anisakis species larvae from fishes of the Japanese waters. Parasitol Int 2011; 60: 223-226. https://doi.org/10.1016/j.parint.2011.03.002

Cited by

  1. Anisakiasis Causing Acute Dysentery in Malaysia vol.95, pp.2, 2015, https://doi.org/10.4269/ajtmh.16-0007
  2. Molecular Identification of Anisakis Larvae Extracted by Gastrointestinal Endoscopy from Health Check-up Patients in Korea vol.57, pp.2, 2015, https://doi.org/10.3347/kjp.2019.57.2.207
  3. Anisakid Larvae from Anchovies in the South Coast of Korea vol.57, pp.6, 2015, https://doi.org/10.3347/kjp.2019.57.6.699
  4. Genera and Species of the Anisakidae Family and Their Geographical Distribution vol.10, pp.12, 2015, https://doi.org/10.3390/ani10122374
  5. First morphological and molecular identification of third-stage larvae of Anisakis typica (Nematoda: Anisakidae) from marine fishes in Vietnamese water vol.53, pp.None, 2021, https://doi.org/10.21307/jofnem-2021-010