journal article·2021-12-05Open access

Prevalence of Anisakis Larvae in Different Fish Species in Southern Albania: Five-Year Monitoring (2016–2020)

Enkeleda Ozuni, Ani Vodica, Marta Castrica, Gabriele Brecchia, Giulio Curone, Stella Agradi, Dino Miraglia, Laura Menchetti, Claudia M. Balzaretti, Egon Andoni

Applied Sciences· Volume 11· Issue 23

Abstract

Anisakidae are nematodes that commonly parasitize in the coelomic cavity and viscera of several fish species. They can be found in flesh, which is why they have an important economic and public health impact. The aim of the current work was to assess the presence and prevalence of Anisakis larvae in fish species caught in the coastal area of the Karaburun Peninsula in Vlora Bay (Albania). A total of 856 of wild teleosts and 219 specimens of farmed fish were collected over a 5-year period (from 2016 to 2020). The results showed that out of a total of 1075 analyzed samples, 361 (33.58%) were parasitized with L3 larvae. In particular, only Solea vulgaris returned negative results, while Sparus aurata, Dicentrarchus labrax, and Sardinella aurita showed the lowest prevalence (4.55%, 9.17%, and 10.53%, respectively) and mean abundance (0.84, 1.19, and 0.92, respectively). Conversely, Scomber japonicus and Scomber scombrus showed the highest prevalence (74.07% and 68.00%, respectively) and mean abundance (188.24 and 249.82, respectively). The data suggest that the coastal area of the Karaburun Peninsula (southern Albania) may be a high-risk area for zoonotic diseases, and the consumption of raw or undercooked fish caught in the Vlora district could result in the acquisition of human anisakiasis. For these reasons, it is necessary to improve the surveillance plan.
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Research context

OpenAlex topics: Parasite Biology and Host Interactions

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Veterinary Faculty of Tirana, Department of Public Health, Agricultural University of Tirana. Rr “Pajsi Vodica”, Koder-Kamez, 1029 Tirana, Albania

Food Safety and Veterinary Institute, Rr “Aleksander Moisiu” No 82, 1005 Tirana, Albania

Department of Health, Animal Science and Food Safety “Carlo Cantoni”, University of Milan, Via Dell’ Università 6, 26900 Lodi, Italy

Department of Veterinary Medicine, University of Milan, Via dell’Università 6, 26900 Lodi, Italy

Department of Veterinary Medicine, University of Perugia, Via San Costanzo 4, 06126 Perugia, Italy

Department of Agricultural and Food Sciences, Alma Mater Studiorum University of Bologna, Viale Fanin 46, 40127 Bologna, Italy

References (58)

Show source-provided references
1. A review on role of fish in human nutrition with special emphasis to essential fatty acid
2. FAO—Food and Agricolture Organizations (2018). The State of World Fisheries and Aquaculture 2018—Meeting the Sustainable 340 Development Goals, FAO. Available online: http://www.fao.org/3/i9540en/i9540en.pdf.
3. WHO—World Health Organization (2012). Soil-Transmitted Helminths, World Health Organization. Available online: http://www.who.int/intestinal_worms/en/.
4. Anisakis notification in fish: An assessment of the cases reported in the European Union rapid alert system for food and feed (RASFF) database10.1016/j.foodcont.2021.107913 ↗
5. (2020). Orphanet Report Series Prevalence and incidence of rare diseases. Orphanet Rep. Ser. Rare Dis. Collect., 1, 1–94.
6. Anisakis Nematodes in Fish and Shellfish- from infection to allergies10.1016/j.ijppaw.2019.04.007 ↗
7. Anisakiasis and gastroallergic reactions associated with Anisakis pegreffii infection, Italy10.3201/eid1903.121017 ↗
8. Molecular epidemiology of anisakis and anisakiasis: An ecological and evolutionary road map10.1016/bs.apar.2017.12.001 ↗
9. Reviewing biodiversity and epidemiological aspects of anisakid nematodes from the North-east Atlantic Ocean10.1017/S0022149X1700027X ↗
10. Anisakis—A food-borne parasite that triggers allergic host defences10.1016/j.ijpara.2013.08.001 ↗
11. Effects of anisakid nematodes Anisakis simplex (s.l.), Pseudoterranova decipiens (s.l.) and Contracaecum osculatum (s.l.) on fish and consumer health10.1016/j.fawpar.2016.07.003 ↗
12. Standardized nomenclature of animal parasitic diseases (SNOAPAD)10.1016/0304-4017(88)90148-3 ↗
13. Human health, legislative and socioeconomic issues caused by the fish-borne zoonotic parasite Anisakis: Challenges in risk assessment10.1016/j.tifs.2019.02.013 ↗
14. Anisakis simplex: From obscure infectious worm to inducer of immune hypersensitivity10.1128/CMR.00012-07 ↗
15. Anisakis simplex: Dangerous—dead and alive?10.1016/S1471-4922(01)02152-3 ↗
16. Epidemiology and management of foodborne nematodiasis in the European Union, systematic review 2000–201610.1080/20477724.2018.1487663 ↗
17. Review of Hysterothylacium and Iberingascaris (both previously Thynnascaris) (Nematoda: 372 Anisakidae) from the northern gulf of Mexico
18. EFSA Panel on Biological Hazards (BIOHAZ) (2010). Scientific opinion on risk assessment of parasites in fishery products. EFSA J., 8, 1543.10.2903/j.efsa.2010.1543 ↗
19. A case of anisakiasis invading the stomach and the colon at the same time after eating anchovies10.5946/ce.2013.46.3.293 ↗
20. Anisakidosis: Perils of the Deep10.1086/656238 ↗
21. The Impact of the Gastronomic Offer in Choosing Tourism Destination: The Case of Albania
22. Moravec, F. (1994). Parasitic Nematodes of Freshwater Fishes of Europe, Kluwer Academic Publishers.
23. Optimization of the pepsin digestion method for anisakids inspection in the fishing industry10.1016/j.vetpar.2012.09.015 ↗
24. ISS-Istituto Superiore di Sanità (2021, October 04). European Union Reference Laboratory for Parasites. Available online: https://ec.europa.eu/food/system/files/2016-10/oc_eurl_wp_2013_parasites_in_particular_trichinella_echinococcus_and_anisakis.pdf.
25. Parasitology meets ecology on its own terms: Margolis et al. revisited10.2307/3284227 ↗
26. Debenedetti, Á.L., Madrid, E., Trelis, M., Codes, F.J., Gil-Gómez, F., Sáez-Durán, S., and Fuentes, M.V. (2019). Prevalence and risk of anisakid larvae in fresh fish frequently consumed in Spain: An overview. Fishes, 4.10.3390/fishes4010013 ↗
27. Quantifying parasites in samples of hosts10.1645/0022-3395(2000)086[0228:QPISOH]2.0.CO;2 ↗
28. Epidemiological scenario of anisakidosis in Spain based on associated hospitalizations: The tip of the iceberg10.1093/cid/ciy853 ↗
29. Assessing the risk of an emerging zoonosis of worldwide concern: Anisakiasis10.1038/srep43699 ↗
30. Pathogenic potential of Anisakis L3 after freezing in domestic freezers10.1016/j.foodcont.2017.07.010 ↗
31. Inactivation of Anisakis simplex larvae in raw fish using high hydrostatic pressure treatments10.1016/j.foodcont.2009.05.013 ↗
32. Antigenicity of Anisakis simplex s.s. L3 in parasitized fish after heating conditions used in the canning processing10.1002/jsfa.6763 ↗
33. Helminth parasites of digestive tract of some teleost fish caught in the Dardanelles at Çanakkale, Turkey10.2478/s11687-007-0035-3 ↗
34. Hysterothylacium 412 aduncum (Nematoda, Anisakidae) with a new host record from the common sole Solea solea (Soleidae) and its role as a 413 biological indicator of pollution10.1007/s00436-014-4213-1 ↗
35. Qualitative risk assessment of introduction of anisakid larvae in Atlantic salmon (Salmo salar) farms and commercialization of products infected with viable nematodes10.1016/j.foodcont.2016.04.058 ↗
36. Nematode infections of maricultured and wild fishes in Danish waters: A comparative study10.1016/j.aquaculture.2009.09.024 ↗
37. Anisakid larva in the viscera of a farmed Atlantic salmon (Salmo salar)10.1016/j.aquaculture.2008.04.006 ↗
38. Anisakidae infection in fish of the Aegean Sea10.1016/j.vetpar.2011.09.007 ↗
39. Ecology and genetic structure of zoonotic Anisakis spp. from adriatic commercial fish species10.1128/AEM.03561-13 ↗
40. Molecular identification of Anisakis species (Nematoda: Anisakidae) from marine fishes collected in Turkish waters10.1016/j.vetpar.2014.01.005 ↗
41. Molecular and epidemiological data on Anisakis spp. (Nematoda: Anisakidae) in commercial fish caught off northern Sardinia (western Mediterranean Sea)10.1016/j.vetpar.2014.02.003 ↗
42. Epidemiology and molecular identification of Anisakis pegreffii (Nematoda: Anisakidae) in the horse mackerel Trachurus trachurus from northern Morocco10.1017/S0022149X13000102 ↗
43. 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, Portugal10.1079/JOH2002156 ↗
44. The diet of blue whiting, hake, horse mackerel and mackerel off Portugal10.1046/j.1439-0426.2002.00297.x ↗
45. Distribution of Anisakis simplex in fish caught in the Ligurian Sea10.1007/s004360000202 ↗
46. Anisakis spp. burden in Trachurus trachurus10.2478/s11687-012-0003-4 ↗
47. Prevalence of anisakid parasites in fish collected from Apulia region (Italy) and quantification of nematode larvae in flesh10.1016/j.ijfoodmicro.2018.12.025 ↗
48. Anisakis species composition and infection characteristics in Atlantic mackerel, Scomber scombrus, from major European fishing grounds—Reflecting changing fish host distribution and migration pattern10.1016/j.fishres.2017.07.030 ↗
49. Potential risk analysis of human anisakiasis through the consumption of mackerel, Scomber scombrus, sold at Spanish supermarkets10.1016/j.foodcont.2016.02.025 ↗
50. Anisakis pegreffii (Nematoda: Anisakidae) in European anchovy Engraulis encrasicolus from the Mediterranean Sea: Fishing ground as a predictor of parasite distribution10.1016/j.fishres.2017.03.020 ↗
51. Anisakisasis in anchovies (Engraulis encrasicolus) and sardines (Sardina pilchardus) caught along the Adriatic Coast
52. Larval migration of the zoonotic parasite Anisakis pegreffii (Nematoda: Anisakidae) in European anchovy, Engraulis encrasicolus: Implications to seafood safety10.1016/j.foodcont.2015.04.043 ↗
53. Do captive conditions favor shedding of parasites in the reared Atlantic bluefin tuna (Thunnus thynnus)?10.1016/j.parint.2010.09.007 ↗
54. Risk factors for human Anisakis infection and association between the geographic origins of Scomber japonicus and anisakid nematodes10.1016/j.ijfoodmicro.2009.10.001 ↗
55. Detection of ascaridoid nematode parasites in the important marine food-fish Conger myriaster (Brevoort) (Anguilliformes: Congridae) from the Zhoushan Fishery, China10.1186/s13071-018-2850-4 ↗
56. Anisakis simplex (s.s.) larvae in wild Alaska salmon: No indication of post-mortem migration from viscera into flesh10.3354/dao02317 ↗
57. The abundance of Anisakis simplex L3 in the body-cavity and flesh of marine teleosts10.1016/0020-7519(84)90030-4 ↗
58. Nematode larvae in fish on the German market 20 years of consumer related research