Parasites, Hosts and Diseases

  • 제49권1호
  • /
  • Pages.39-44
  • /
  • 2011
  • /
  • 2982-5164(pISSN)
  • /
  • 1738-0006(eISSN)
대한기생충학·열대의학회 (The Korea Society for Parasitology and Tropical Medicine)
권호 표지
DOI QR코드

DOI QR Code

Anisakis simplex Larvae: Infection Status in Marine Fish and Cephalopods Purchased from the Cooperative Fish Market in Busan, Korea

  • Choi, Seon-Hee (Department of Parasitology, School of Medicine, Pusan National University) ;
  • Kim, Jung (Department of Parasitology and Genetics, Kosin University College of Medicine) ;
  • Jo, Jin-Ok (Department of Parasitology and Genetics, Kosin University College of Medicine) ;
  • Cho, Min-Kyung (Department of Parasitology, School of Medicine, Pusan National University) ;
  • Yu, Hak-Sun (Department of Parasitology, School of Medicine, Pusan National University) ;
  • Cha, Hee-Jae (Department of Parasitology and Genetics, Kosin University College of Medicine) ;
  • Ock, Mee-Sun (Department of Parasitology and Genetics, Kosin University College of Medicine)
  • 투고 : 2010.11.09
  • 심사 : 2011.01.25
  • 발행 : 2011.03.15
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

The infection status of marine fish and cephalopods with Anisakis simplex third stage larva (L3) was studied over a period of 1 year. A total of 2,537 specimens, which consisted of 40 species of fish and 3 species of cephalopods, were purchased from the Cooperative Fish Market in Busan, Korea, from August 2006 to July 2007. They were examined for A. simplex L3 from the whole body cavity, viscera, and muscles. A. simplex L3 were confirmed by light microscopy. The overall infection rate reached 34.3%, and average 17.1 larvae were parasitized per infected fish. Fish that recorded the highest infection rate was Lophiomus setigerus (100%), followed by Liparis tessellates (90%), Pleurogrammus azonus (90%), and Scomber japonicus (88.7%). The intensity of infection was the highest in Gadus macrocephalus (117.7 larvae per fish), followed by S. japonicus (103.9 larvae) and L. setigerus (54.2 larvae). Although abundance of A. simplex L3 was not seasonal in most of the fish species, 10 of the 16 selected species showed the highest abundance in February and April. A positive correlation between the intensity of L3 infection and the fish length was obvious in S. japonicus and G. macrocephalus. It was likely that A. simplex L3 are more frequently infected during the spring season in some species of fish. Our study revealed that eating raw or undercooked fish or cephalopods could still be a source of human infection with A. simplex L3 in Korea.

키워드

참고문헌

  1. Abollo E, Gestal C, Pascual S. Anisakis infestation in marine fish and cephalopods from Galician waters: an updated perspective. Parasitol Res 2001; 87: 492-499. https://doi.org/10.1007/s004360100389
  2. Costa G, Pontes T, Mattiucci S, D'Amélio S. The occurrence and infection dynamics of Anisakis larvae in the black-scabbard fish, Aphanopus carbo, chub mackerel, Scomber japonicus, and oceanic horse mackerel, Trachurus picturatus from Madeira, Portugal. J Helminthol 2003; 77: 163-166. https://doi.org/10.1079/JOH2002156
  3. Ma HW, Jiang TJ, Quan FS, Chen XG, Wang HD, Zhang YS, Cui MS, Zhi WY, Jiang DC. The infection status of anisakid larvae in marine fish and cephalopods from the Bohai Sea, China and their taxonomical consideration. Korean J Parasitol 1997; 35: 19-24.
  4. Chun SK, Chung BK, Ryu BS. Studies on Anisakis sp. (1) On the infection state of Anisakis-like larvae isolated from various marine fishes. Korean J Fish Aquat Sci 1968; 1: 1-6 (in Korean).
  5. Chai JY, Chu YM, Sohn WM, Lee SH. Larval anisakids collected from the yellow corvina in Korea. Korean J Parasitol 1986; 24: 1-11.
  6. 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
  7. 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) caught from Taepo port, Kang won Do. Korean J Rural Med 1990; 15: 27-32.
  8. 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. https://doi.org/10.3347/kjp.1995.33.2.95
  9. Bouree P, Paugam A, Petithory JC. Anisakidosis: report of 25 cases and review of the literature. Comp Immunol Microbiol Infect Dis 1995; 18: 75-84. https://doi.org/10.1016/0147-9571(95)98848-C
  10. Im KI, Shin HJ, Kim BH, Moon SI. Gastric anisakiasis cases in Cheju-do, Korea. Korean J Parasitol 1995; 33: 179-186. https://doi.org/10.3347/kjp.1995.33.3.179
  11. Noh JH, Kim B, Kim SM, Ock M, Park MI, Goo JY. A case of acute gastric anisakiasis provoking severe clinical problems by multiple infections. Korean J Parasitol 2003; 41: 97-100. https://doi.org/10.3347/kjp.2003.41.2.97
  12. Kim SG, Jo YJ, Park YS, Kim SH, Song MH, Lee HH, Kim JS, Ryou JW, Joo JE, Kim DH. Four cases of gastric submucosal mass suspected as anisakiasis. Korean J Parasitol 2006; 44: 81-86.
  13. Yoon SW, Yu JS, Park MS, Shim JY, Kim HJ, Kim KW. CT findings of surgically verified acute invasive small bowel anisakiasis resulting in small bowel obstruction. Yonsei Med J 2004; 45: 739-742. https://doi.org/10.3349/ymj.2004.45.4.739
  14. Alonso A, Daschner A, Moreno-Ancillo A. Anaphylaxis with Anisakis simplex in the gastric mucosa. N Engl J Med 1997; 337: 350-351.
  15. Arrieta I, del Barrio M, Vidarte L, del Pozo V, Pastor C, Gonzalez-Cabrero J, Cárdaba B, Rojo M, Mínguez A, Cortegano I, Gallardo S, Aceituno E, Palomino P, Vivanco F, Lahoz C. Molecular cloning and characterization of an IgE-reactive protein from Anisakis simplex: Ani s 1. Mol Biochem Parasitol 2000; 107: 263-268. https://doi.org/10.1016/S0166-6851(00)00192-4
  16. Mattiucci S. Parasites as biological tags in population studies of demersal and pelagic fish species. Parassitologia 2006; 48: 23-25.
  17. Smith JW. Anisakis simplex (Rudolphi, 1809, det. Krabbe, 1878) (Nematoda: Ascaridoidea): morphology and morphometry of larvae from euphausiids and fish, and a review of the life-history and ecology. J Helminthol 1983; 57: 205-224. https://doi.org/10.1017/S0022149X00009512
  18. Bush AO, Lafferty KD, Lotz JM, Shostak AW. Parasitology meets ecology on its own terms: Margolis et al. revisited. J Parasitol 1997; 83: 575-583. https://doi.org/10.2307/3284227
  19. 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.
  20. Stromnes E, Andersen K. Spring rise of whaleworm (Anisakis simplex; Nematoda, Ascaridoidea) third-stage larvae in some fish species from Norwegian waters. Parasitol Res 2000; 86: 619-624. https://doi.org/10.1007/PL00008541
  21. Andersen K. Hysterothylacium aduncum (Rudolphi, 1862) infection in cod from the third- and fourth-stage larvae as well as worms. Parasitol Res 1993; 79: 67-72. https://doi.org/10.1007/BF00931220
  22. Stavn RH. The horizontal-vertical distribution hypothesis: Langmuir circulations and Daphnia distributions. Limnol Oceanogr 1971; 16: 453-466. https://doi.org/10.4319/lo.1971.16.2.0453

피인용 문헌

  1. Seroprevalence of Antibodies against Anisakis simplex Larvae among Health-Examined Residents in Three Hospitals of Southern Parts of Korea vol.49, pp.2, 2011, https://doi.org/10.3347/kjp.2011.49.2.139
  2. Larval Anisakid Infections in Marine Fish from Three Sea Areas of the Republic of Korea vol.50, pp.4, 2012, https://doi.org/10.3347/kjp.2012.50.4.295
  3. A rapid PCR-RFLP method for the identification of Lophius species vol.235, pp.2, 2012, https://doi.org/10.1007/s00217-012-1754-3
  4. Anisakidosis in Korea; Changes Over the Last Decade vol.27, pp.2, 2012, https://doi.org/10.7180/kmj.2012.27.2.73
  5. Molecular Analysis of Anisakis Type I Larvae in Marine Fish from Three Different Sea Areas in Korea vol.52, pp.4, 2014, https://doi.org/10.3347/kjp.2014.52.4.383
  6. Anisakis pegreffii Larvae in Sea Eels (Astroconger myriaster) from the South Sea, Republic of Korea vol.53, pp.3, 2011, https://doi.org/10.3347/kjp.2015.53.3.349
  7. Inactivation of Anisakis simplex L3 in the flesh of white spotted conger (Conger myriaster) by high hydrostatic pressure and its effect on quality vol.33, pp.6, 2016, https://doi.org/10.1080/19440049.2016.1183108
  8. Simultaneous Detection and Prevalence of Allergens in Anisakis Species Isolated from Marine Fishes vol.79, pp.5, 2016, https://doi.org/10.4315/0362-028x.jfp-15-539
  9. Endosonographic Findings and the Natural Course of Chronic Gastric Anisakiasis: A Single-Center Experience vol.2018, pp.None, 2018, https://doi.org/10.1155/2018/8562792
  10. Seafood-Borne Parasitic Diseases: A “One-Health” Approach Is Needed vol.4, pp.1, 2019, https://doi.org/10.3390/fishes4010009
  11. Assessment of parasite virulence in a natural population of a planktonic crustacean vol.19, pp.1, 2011, https://doi.org/10.1186/s12898-019-0230-3