DOI QR코드

DOI QR Code

Molecular Analysis of Anisakis Type I Larvae in Marine Fish from Three Different Sea Areas in Korea

  • Sohn, Woon-Mok (Department of Parasitology and Tropical Medicine, and Institute of Health Sciences, Gyeongsang National University School of Medicine) ;
  • Kang, Jung-Mi (Department of Parasitology and Tropical Medicine, and Institute of Health Sciences, Gyeongsang National University School of Medicine) ;
  • Na, Byoung-Kuk (Department of Parasitology and Tropical Medicine, and Institute of Health Sciences, Gyeongsang National University School of Medicine)
  • Received : 2014.03.21
  • Accepted : 2014.05.26
  • Published : 2014.08.31

Abstract

Anisakiasis, a human infection of Anisakis L3 larvae, is one of the common foodborne parasitic diseases in Korea. Studies on the identification of anisakid larvae have been performed in the country, but most of them have been focused on morphological identification of the larvae. In this study, we analyzed the molecular characteristics of 174 Anisakis type I larvae collected from 10 species of fish caught in 3 different sea areas in Korea. PCR-RFLP and sequence analyses of rDNA ITS and mtDNA cox1 revealed that the larvae showed interesting distribution patterns depending on fish species and geographical locations. Anisakis pegreffii was predominant in fish from the Yellow Sea and the South Sea. Meanwhile, both A. pegreffii and A. simplex sensu stricto (A. simplex s.str.) larvae were identified in fish from the East Sea, depending on fish species infected. These results suggested that A. pegreffii was primarily distributed in a diverse species of fish in 3 sea areas around Korea, but A. simplex s.str. was dominantly identified in Oncorhynchus spp. in the East Sea.

Keywords

References

  1. 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
  2. Audicana MT, Kennedy MW. Anisakis simplex: from obscure infectious worm to inducer of immune hypersensitivity. Clin Microbiol Rev 2008; 21: 360-379. https://doi.org/10.1128/CMR.00012-07
  3. Hochberg NS, Hamer DH. Anisakidosis: perils of the deep. Clin Infect Dis 2010; 51: 806-812. https://doi.org/10.1086/656238
  4. Sohn WM, Chai JY. Anisakiosis (Anisakidosis). In Palmer SR et al. eds, Oxford Textbook of Zoonoses-Biology, Clinical Practice, and Public Health Control, 2nd ed. Oxford, UK. Oxford Univer sity Press. 2011, p 774-786.
  5. Choi SH, Kim J, Jo JO, Cho MK, Yu HS, Cha HJ, Ock MS. Anisakis simplex larvae: infection status in marine fish and cephalo pods 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
  6. Setyobudi E, Jeon CH, Lee CH, Seong KB, 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
  7. 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
  8. Setyobudi E, Jeon CH, Choi K, Lee SI, Lee CI, Kim JH. Molecular identification of anisakid nematodes third stage larvae isolated from common squid (Todarodes pacificus) in Korea. Ocean Sci J 2013; 48: 197-205. https://doi.org/10.1007/s12601-013-0016-z
  9. 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
  10. Hu M, D'Amelio S, Zhu X, Paggi L, Gasser R. Mutation scanning for sequence variation in three mitochondrial DNA regions for members of the Contracaecum osculatum (Nematoda: Ascaridoidea) complex. Electrophoresis 2001; 22: 1069-1075. https://doi.org/10.1002/1522-2683()22:6<1069::AID-ELPS1069>3.0.CO;2-T
  11. 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
  12. Tamura K, Dudley J, Nei M, Kumar S. MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol 2007; 24: 1596-1599 https://doi.org/10.1093/molbev/msm092
  13. Berland B. Nematodes from some Norwegian marine fishes. Sarsia 1961; 2: 1-50.
  14. Iglesias R, D'Amelio S, Ingrosso S, Farjallah S, Martines-Cedeira JA, Garcia-Esteves JM. Molecular and morphological evidence for the occurrence of Anisakis sp. A (Nematoda, Anisakidae) in Blainville's beaked whale Mesoplodon densirotris. J Helminthol 2008; 82: 305-308. https://doi.org/10.1017/S0022149X08996978
  15. Mattiucci S, Nascetti G. Advances and trends in the molecular systematics of anisakid nematodes, with implications for their evolutionary ecology and host-parasite co-evolutionary processes. Adv Parasitol 2008; 66: 47-248. https://doi.org/10.1016/S0065-308X(08)00202-9
  16. Arizono N, Yamada M, Tegoshi T, Yoshikawa M. Anisakis simplex sensu stricto and Anisakis pegreffii: biological characteristics and pathogenic potential in human anisakiasis. Foodborne Pathog Dis 2012; 9: 1-5. https://doi.org/10.1089/fpd.2011.0910
  17. Pontes T, D'Amelio S, Costa G, Paggi L. Molecular characterization of larval anisakid nematodes from marine fishes of Madeira by a PCR-based approach, with evidence for a new species. J Parasitol 2005; 91: 1430-1434. https://doi.org/10.1645/GE-565R1.1
  18. Chen Q, Yu HQ, Lun ZR, Chen XG, Song HQ, Lin RQ, Zhu XQ. Specific PCR assays for the identification of common anisakid nematodes with zoonotic potential. Parasitol Res 2008; 104: 79-84. https://doi.org/10.1007/s00436-008-1161-7
  19. Abe N, Ohya N, Yanagiguchi R. Molecular characterization of Anisakis pegreffii larvae in pacific cod in Japan. J Helminthol 2005; 79: 303-306. https://doi.org/10.1079/JOH2005290
  20. Umehara A, Kawakami Y, Ooi HK, Uchida A, Ohmae H, Sugiyama H. Molecular identification of Anisakis type I larvae isolated from hairtail fish off the coasts of Taiwan and Japan. Int J Food Microbiol 2010; 143: 161-165. https://doi.org/10.1016/j.ijfoodmicro.2010.08.011
  21. Du C, Zhang L, Shi M, Ming Z, Hu M, Gasser RB. Elucidating the identity of Anisakis larvae from a broad range of marine fishes from the Yellow Sea, China, using a combined electrophoretic-sequencing approach. Electrophoresis 2010; 31: 654-658. https://doi.org/10.1002/elps.200900531
  22. Quiazon KMA, Yoshinaga T, Ogawa K. Experimental challenge of Anisakis simplex sensu stricto and Anisakis pegreffii (Nematoda: Anisakidae) in rainbow trout and olive flounder. Parasitol Int 2011; 60: 126-131. https://doi.org/10.1016/j.parint.2010.11.007
  23. Abollo E, Paggi L, Pascual S, D'Amelio S. Occurrence of recombinant genotypes of Anisakis simplex s.s. and Anisakis pegreffii (Nematoda: Anisakidae) in an area of sympatry. Infect Genet Evol 2003; 3: 175-181. https://doi.org/10.1016/S1567-1348(03)00073-X
  24. Martin-Sanchez J, Artacho-Reinoso ME, Diaz-Gavilan M, Valero-Lopez A. Structure of Anisakis simplex s. l. populations in a region sympatric for A. pegreffii and A. simplex s. s. Absence of reproductive isolation between both species. Mol Biochem Parasitol 2005; 141: 155-162. https://doi.org/10.1016/j.molbiopara.2005.02.005
  25. 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
  26. D'Amelio S, Mathiopoulos KD, Brandonisio O, Lucarelli G, Doronzo F, Paggi L. Diagnosis of a case of gastric anisakidosis by PCR-based restriction fragment length polymorphism analysis. Parassitologia 1999; 41: 591-593.
  27. Fumarola L, Monno R, Ierardi E, Rizzo G, Giannelli G, Lalle M, Pozio E. Anisakis pegreffi etiological agent of gastric infections in two Italian women. Foodborne Pathog Dis 2009; 6: 1157-1159. https://doi.org/10.1089/fpd.2009.0325
  28. Suzuki J, Murata R, Hosaka M, Araki J. Risk factors for human Anisakis infection and association between the geographic origins of Scomber japonicus and anisakid nematodes. Int J Food Microbiol 2010; 137: 88-93. https://doi.org/10.1016/j.ijfoodmicro.2009.10.001
  29. Lee EJ, Kim YC, Jeong HG, Lee OJ. The mucosal changes and influencing factors in upper gastrointestinal anisakiasis: analysis of 141 cases. Korean J Gastroenterol 2009; 53: 90-97 (in Korean).
  30. Do KR, Cho YS, Kim HK, Hwang BH, Shin EJ, Jeong HB, Kim SS, Chae HS, Choi MG. Intestinal helminthic infections diagnosed by colonoscopy in a regional hospital during 2001-2008. Korean J Parasitol 2010; 48: 75-78. https://doi.org/10.3347/kjp.2010.48.1.75
  31. Kim T, Song HJ, Jeong SU, Choi EK, Cho YK, Kim HU, Song BC, Kim KS, Kim BS, Kim YR. Comparison of the clinical characteristics of patients with small bowel and gastric anisakiasis in jeju island. Gut Liver 2013; 7: 23-29. https://doi.org/10.5009/gnl.2013.7.1.23

Cited by

  1. Anisakis pegreffii Larvae in Sea Eels (Astroconger myriaster) from the South Sea, Republic of Korea vol.53, pp.3, 2014, https://doi.org/10.3347/kjp.2015.53.3.349
  2. Anisakiasis: Report of 15 Gastric Cases Caused by Anisakis Type I Larvae and a Brief Review of Korean Anisakiasis Cases vol.53, pp.4, 2014, https://doi.org/10.3347/kjp.2015.53.4.465
  3. Occurrence of Anisakis Larvae in Commercial Fish along the Northern Coast of Taiwan vol.10, pp.3, 2014, https://doi.org/10.3923/jp.2015.79.91
  4. Environmental variables and definitive host distribution: a habitat suitability modelling for endohelminth parasites in the marine realm vol.6, pp.None, 2014, https://doi.org/10.1038/srep30246
  5. An Overview of Fish-borne Nematodiases among Returned Travelers for Recent 25 Years- Unexpected Diseases Sometimes Far Away from the Origin vol.56, pp.3, 2018, https://doi.org/10.3347/kjp.2018.56.3.215
  6. Occurrence and molecular identification of Anisakis larval type 1 (Nematoda: Anisakidae) in marketed fish in Egypt vol.44, pp.3, 2014, https://doi.org/10.1007/s12639-020-01222-8
  7. Increasing intensities of Anisakis simplex third-stage larvae (L3) in Atlantic salmon of coastal waters of Scotland vol.13, pp.1, 2014, https://doi.org/10.1186/s13071-020-3942-5