HOST SPECIFICITY, INFECTION DYNAMICS, AND ALLERGENICITY IN Anisakis SPP. INFESTATION: A REVIEW
DOI:
https://doi.org/10.46754/umtjur.v6i2.459Keywords:
Anisakis, fish, allergen, infection dynamics, host specificityAbstract
Fish and seafood are important in providing protein to human diets. However, they are susceptible to contamination by various parasites, such as nematodes, cestodes, and trematodes. Among these, Anisakis spp. and other species of trematodes belonging to the Anisakidae family are commonly identified in fish and shellfish, posing a significant health risk. This contamination poses a substantial risk to public health, particularly with the increasing prevalence of these parasites in marine fish. The globalisation of cuisines, including sushi, is one of the factors causing this development. The risk of Anisakis contamination has increased due to the global popularity of sushi, a form of Japanese food that features raw or undercooked fish. Gastric anisakiasis is the primary infection in humans, caused by the penetration of L3 larvae into the gastric wall. However, the indefinite symptoms associated with anisakiasis make precise identification challenging, complicating efforts to effectively treat this health issue. This study reviewed the host specificity, risk factors, infection mechanisms, and infestation areas of Anisakis spp. Various reputable sources, including Google Scholar, PubMed Central, ScienceDirect, Springer Link, and the Wiley Online Library, were used to explore the diverse host preferences and the impact of environmental changes. The larvae of Anisakis spp. exhibit diverse host preferences and environmental changes like global warming make hosts more vulnerable. Inadvertent exposure to these parasites occurs when individuals consume raw or undercooked fish and seafood. An extremely serious threat is posed by allergic anisakiasis, characterised by severe symptoms such as respiratory arrest, shock, and collapse. Research focusing on bioactive substances capable of blocking or neutralising the excretions and secretions of Anisakis sp. should be encouraged. Metalloproteinases (MMPs) and serine proteases, in particular, show promise for minimising adverse effects and reducing dependency on medication in treating allergic anisakiasis. Further research and intervention techniques are essential if health issues associated with Anisakis exist.
References
Adroher-Auroux., F. J., & Benitez-Rodriguez. (2020). Anisakiasis and Anisakis: An underdiagnosed emerging disease and its main etiological agents. Research in Veterinary Science, 132, 535-545. https:// doi.org/10.1016/j.rvsc.2020.08.003 DOI: https://doi.org/10.1016/j.rvsc.2020.08.003
Aibinu, I. E., Smooker, P. M., & Lopata, A. L. (2019). Anisakis Nematodes in fish and shellfish- from infection to allergies. International Journal for Parasitology: Parasites and Wildlife (IJP-PAW), 9, 384- 393. https://doi.org/10.1016/j.ijppaw.2019. 04.007 DOI: https://doi.org/10.1016/j.ijppaw.2019.04.007
Amarnath, S., Deeb, L., Philipose, J., Zheng, X., & Gumaste, V. A. (2021). A comprehensive review of infectious granulomatous diseases of the gastrointestinal tract. Gastroenterology Research and Practice, 2021, 1-20. https:// doi.org/10.1155/2021/8167149 DOI: https://doi.org/10.1155/2021/8167149
Audicana, T., Italo, G., & Areso, N. (2017). Anisakis simplex, a new hero in the Anaphylaxis Scene. SM Emergency Medicine and Critical Care Journal, 1, 1-6. https://doi.org/10.36876/smem.1008 DOI: https://doi.org/10.36876/smem.1008
Baird, F. J., Gasser, R. B., Jabbar, A., & Lopata, A. L. (2014). Foodborne anisakiasis and allergy. Molecular and Cellular Probes, 28, 167-174. https://doi.org/10.1016/j.mcp. 2014.02.003 DOI: https://doi.org/10.1016/j.mcp.2014.02.003
Bao, M., Pierce, G. J., Strachan, N. J. C., Pascual, S., González-Muñoz, M., & Levsen, A. (2019). Human health, legislative and socioeconomic issues caused by the fish-borne zoonotic parasite Anisakis: Challenges in risk assessment. Trends in Food Science and Technology, 86, 298-310. https://doi.org/10.1016/j.tifs.2019.02.013 DOI: https://doi.org/10.1016/j.tifs.2019.02.013
Baptista-Fernandes, T., Rodrigues, M., Castro, I., Paixão, P., Pinto-Marques, P., Roque, L., Belo, S., Ferreira, P. M., Mansinho, K., & Toscano, C. (2017). Human gastric hyperinfection by Anisakis simplex: A severe and unusual presentation and a brief review. International Journal of Infectious Diseases, 64, 38-41. DOI: https://doi.org/10.1016/j.ijid.2017.08.012
Caldeira, A. J. R., Pereira, A. C. P., & Santos, M. J. (2021). Anisakis notification in fish: An assessment of the cases reported in the European Union Rapid Alert System for Food and Feed (RASFF) database. Food Control, 124, 107913. https://doi.org/ 10.1016/j.foodcont.2021.107913 DOI: https://doi.org/10.1016/j.foodcont.2021.107913
Carvalho, E. L., de, Santana, R. L. S., Gonçalves, E. C., Pinheiro, R. H. da S., & Giese, E. G. (2020). First report of Anisakis sp. (Nematoda: Anisakidae) parasitizing Muscovy duck in Marajó Island, State of Pará, Brazil. Revista Brasileira de Parasitologia Veterinaria, 29, e020319. https://doi.org/10.1590/s1984-29 612020015 DOI: https://doi.org/10.1590/s1984-29612020015
Cavallero, S., Bellini, I., Pizzarelli, A., & D’Amelio, S. (2022). What do In Vitro and In Vivo Models tell us about Anisakiasis? New tools still to be explored. Pathogens, 11(3), 285. https://doi. org/10.3390/pathogens11030285 DOI: https://doi.org/10.3390/pathogens11030285
Cheypanya, V., Wongsawad, P., Wongsawad, C., & Nantarat, N. (2021). Morphological study and molecular epidemiology of Anisakis larvae in mackerel fish. Asian Pacific Journal of Tropical Medicine, 14, 214. https://doi.org/10.4103/1995-7645.315900 DOI: https://doi.org/10.4103/1995-7645.315900
Choi, S. K., Kim, C. K., Kim, S. H., & Jo, D. I. (2017). Anisakiasis involving the oral mucosa. Archives of Craniofacial Surgery, 18, 261-263. https://doi.org/10.7181/acfs. 2017.18.4.261 DOI: https://doi.org/10.7181/acfs.2017.18.4.261
Cong, W., & Elsheikha, H. M. (2021). Biology, epidemiology, clinical features, diagnosis, and treatment of selected fish-borne parasitic zoonoses. Yale Journal of Biology and Medicine, 94, 297-309.
Cunha, J. P. (2021). Mintezol (Thiabendazole) side effects drug centre. RxList. URL Accessed December 20, from https://www. rxlist.com/mintezol-side-effects-drug-center.htm#overview
El Meghanawy, R. A., E. I., E. T., Salim Dalia, A., & Abdel Aziz, A. R. (2021). Epidemiological, morphological, and molecular characterization of Anisakis simplex (sensu stricto) in Clupea harengus from Egypt. Veterinary Parasitology: Regional Studies and Reports, 24, 100574. https://doi.org/10.1016/j.vprsr.2021.100574 DOI: https://doi.org/10.1016/j.vprsr.2021.100574
Fioravanti, M. L., Gustinelli, A., Rigos, G., Buchmann, K., Caffara, M., Pascual, S., & Pardo, M. Á. (2021). Negligible risk of zoonotic anisakid nematodes in farmed fish from European mariculture, 2016 to 2018. Eurosurveillance, 26, 1900717. https:// doi.org/10.2807/1560-7917.ES.2021. 26.2.1900717 DOI: https://doi.org/10.2807/1560-7917.ES.2021.26.2.1900717
Fiorenza, E. A., Wendt, C. A., Dobkowski, K. A., King, T., Pappaionou, M., Rabinowitz, P., Samhouri, J. F., & Wood, C. L. (2020). It’s a wormy world: Meta-analysis reveals several decades of change in the global abundance of the parasitic nematodes Anisakis spp. and Pseudoterranova spp. in marine fishes and invertebrates. Global Change Biology, 26, 2854-2866. https:// doi.org/10.1111/gcb.15048 DOI: https://doi.org/10.1111/gcb.15048
Gentile, A., Amato, T., Gustinelli, A., Fioravanti, M. L., Gambino, D., Randazzo, V., Caracappa, G., Vicari, D., & Arculeo, M. (2021). Helminth infection of the Loggerhead Sea Turtle Caretta caretta along the Coasts of Sicily and the North West Adriatic Sea. Animal (Basel), 11(5), 1408. https://doi.org/10.3390/ani11051408 DOI: https://doi.org/10.3390/ani11051408
Haryadi, L., Suprayitno, E., Aulani, A., Amin, M., & Hariati, A. (2019). Identification of Anisakid nematode L3 larvae infection on Skipjack Tuna (Katsuwonus pelamis L. from Kupang waters, East Nusa Tenggara of Indonesia. Russian Journal of Agricultural and Socio-Economic Sciences (RJOAS), 92, 305-312. https://doi.org/10.18551/rjoas. 2019-08.35 DOI: https://doi.org/10.18551/rjoas.2019-08.35
Hochberg, N. S., & Hamer, D. H. (2010) Anisakidosis: Perils of the deep. Clinical Infectious Diseases, 51, 806-812. https:// doi.org/10.1086/656238 DOI: https://doi.org/10.1086/656238
Joo, S. K., Kim, J. W., Kim, B. G., Kim, W., Lee, J. K., & Lee, K. L. (2019). Clinical and endoscopic features of Colonic Anisakiasis in Korea. Korean Journal of Parasitology, 57, 411-416. https://doi.org/10.3347/kjp. 2019.57.4.411 DOI: https://doi.org/10.3347/kjp.2019.57.4.411
Lee, J. D., Chung, L. Y., Lin, R. J., Wang, J. J., Tu, H. P., & Yen, C. M. (2017). Excretory/ secretory proteases and mechanical movement of Anisakis pegreffii infective larvae in the penetration of BALB/c mice gastrointestine. The Kaohsiung Journal of Medical Sciences, 33, 594-601. DOI: https://doi.org/10.1016/j.kjms.2017.08.002
Łopieńska-Biernat, E., Stryiński, R., Polak, I., Pawlikowski, B., Pawlak, J., & Podolska, M. (2020). Effect of freezing on the metabolic status of L3 larvae of Anisakis simplex s. s. Infect. Genetics Selection Evolution, 82, 104312. https://doi. org/10.1016/j.meegid.2020.104312 DOI: https://doi.org/10.1016/j.meegid.2020.104312
Mangmee, S., Adisakwattana, P., Tipthara, P., Simanon, N., Sonthayanon, P., & Reamtong, O. (2020). Lipid profile of Trichinella papuae muscle-stage larvae. Scientific Reports, 10, 10125. https://doi. org/10.1038/s41598-020-67297-8 DOI: https://doi.org/10.1038/s41598-020-67297-8
Marzano, V., Pane, S., Foglietta, G., Mortera, S. L., Vernocchi, P., Muda, A. O., & Putignani, L. (2020). Mass Spectrometry Based- Proteomic Analysis of Anisakis spp.: A preliminary study towards a new diagnostic tool. Genes (Basel), 11(6), 693. https://doi. org/10.3390/genes11060693 DOI: https://doi.org/10.3390/genes11060693
Mattiucci, S., Paoletti, M., Colantoni, A., Carbone, A., Gaeta, R., Proietti, A., Frattaroli, S., Fazii, P., Bruschi, F., & Nascetti, G. (2017). Invasive anisakiasis by the parasite Anisakis pegreffii (Nematoda: Anisakidae): Diagnosis by real-time PCR hydrolysis probe system and immunoblotting assay. BMC Infectious Diseases, 17, 1-9. https://doi.org/10.1186/ s12879-017-2633-0 DOI: https://doi.org/10.1186/s12879-017-2633-0
McSorley, H. J., & Maizels, R. M. (2012). Helminth infections and host immune. Regulation Clinical Microbiology Reviews, 25(4), 585-608. https://doi:10.1128/CMR. 05040-11 DOI: https://doi.org/10.1128/CMR.05040-11
Mizumura, N., Okumura, S., Tsuchihashi, H., Ogawa, M., & Kawasaki, M. (2018). A second attack of Anisakis: Intestinal Anisakiasis following Gastric Anisakiasis ACG Case Reports Journal, 5, e65. https:// doi.org/10.14309/crj.2018.65 DOI: https://doi.org/10.14309/crj.2018.65
Moneo, I., Carballeda-Sangiao, N., & González- Muñoz, M. (2017). New perspectives on the diagnosis of allergy to Anisakis spp. Current Allergy and Asthma Reports, 17, 27. https:// doi.org/10.1007/s11882-017-0698-x DOI: https://doi.org/10.1007/s11882-017-0698-x
Montalto, M., Miele, L., Marcheggiano, A., Santoro, L., Curigliano, V., Vastola, M., & Gasbarrini, G. (2005). Anisakis infestation: A case of acute abdomen mimicking Crohn’s disease and eosinophilic gastroenteritis. Digestive and Liver Disease, 37, 62-64. https://doi.org/10.1016/j.dld.2004.05.014 DOI: https://doi.org/10.1016/j.dld.2004.05.014
Motran, C. C., Silvane, L., Chiapello, L. S., Theumer, M. G., Ambrosio, L. F., Volpini, X., Celias, D. P., & Cervi, L. (2018). Helminth infections: Recognition and modulation of the immune response by innate immune cells. Frontiers in Immunology, 9, 664. https://doi.org/10.3389/fimmu.2018.00664 DOI: https://doi.org/10.3389/fimmu.2018.00664
Napoletano, C., Mattiucci, S., Colantoni, A., Battisti, F., Zizzari, I. G., Rahimi, H., Nuti, M., & Rughetti, A. (2018). Anisakis pegreffii impacts differentiation and function of human dendritic cells. Parasite Immunology, 40, e12527. https://doi.org/10. 1111/pim.12527 DOI: https://doi.org/10.1111/pim.12527
Nieuwenhuizen, N. E. (2016). Anisakis- Immunology of a foodborne parasitosis. Parasite Immunology, 38, 548-557. https:// doi.org/10.1111/pim.12349 DOI: https://doi.org/10.1111/pim.12349
Pampiglione, S., Rivasi, F., Criscuolo, M., De Benedittis, A., Gentile, A., Russo, S., Testini, M., & Villani, M. (2002). Human Anisakiasis in Italy: A report of eleven new cases. Pathology – Journal Research and Practice, 198, 429-434. https://doi.org /10.1078/0344 -0338-00277 DOI: https://doi.org/10.1078/0344-0338-00277
Polak, I., Łopieńska-Biernat, E., Stryiński, R., Mateos, J., & Carrera, M. (2020). Comparative Proteomics Analysis of Anisakis simplex s.s. - Evaluation of the response of invasive larvae to ivermectin. Genes, 11, 710. https://doi.org/10.3390/gen es11 060710 DOI: https://doi.org/10.3390/genes11060710
Polimeno, L., Lisanti, M. T., Rossini, M., Giacovazzo, E., Polimeno Lucrezia Debellis, L., Ballini., A. Topi, S., & Santacroce, L. (2021). Anisakis allergy: Is aquacultured fish a safe and alternative food to wild-capture fisheries for Anisakis simplex - Sensitized patients? Journal of Biology, 10, 106. https://doi.org/10.3390/ biology 10020106 DOI: https://doi.org/10.3390/biology10020106
Rolbiecki, L. (2002). On the role of paratenic hosts in the life cycle of the nematode Anguillicola crassus in the Vistula Lagoon, Poland. Acta Ichthyologica Et Piscatoria, 32, 109-116. https://doi.org/10.3750/AIP 2002.32.2.01 DOI: https://doi.org/10.3750/AIP2002.32.2.01
Samanta, M., & Choudhary, P. (2019). Chapter 7 - Safety of fish and seafood. In Singh, R. L., Mondal, S. (Eds.), Food safety and human health (pp. 169-187). Academic Press. https://doi.org/10.1016/B978-0-12- 816333-7.00007-2 DOI: https://doi.org/10.1016/B978-0-12-816333-7.00007-2
Sánchez-Alonso, I., Carballeda-Sangiao, N., Rodríguez, S., Tejada, M., Navas, A., Arcos, S. C., González-Muñoz, M., & Careche, M. (2021). Anisakis simplex (s.l.) resistance to the action of gastric enzymes depends upon previous treatments applied to infected fish mince and affects antigen release. Journal of the Science of Food and Agriculture, 101, 3908-3916. https://doi.org/10.1002/js fa.11031 DOI: https://doi.org/10.1002/jsfa.11031
Santoro, M., Badillo, F. J., Mattiucci, S., Nascetti, G., Bentivegna, F., Insacco, G., Travaglini, A., Paoletti, M., Kinsella, J. M., Tomás, J., et al. (2010). Helminth communities of Loggerhead Turtles (Caretta Caretta) from Central and Western Mediterranean Sea: The importance of host’s ontogeny. Parasitology International Journal, 59, 367-375. https://doi.org/ 10.1016/j.parint.2010.04.009 DOI: https://doi.org/10.1016/j.parint.2010.04.009
Santoro, M., Di Nocera, F., Iaccarino, D., Cipriani, P., Guadano Procesi, I., Maffucci, F., Hochscheid, S., Blanco, C., Cerrone, A., Galiero, G., Nascetti, G., & Mattiucci, S. (2018). Helminth parasites of the dwarf sperm whale Kogia sima. Diseases of Aquatic Organisms, 129(3), 175-182. https://doi.org/10.3354/dao03251 DOI: https://doi.org/10.3354/dao03251
Shamsi, S. (2019). Parasite loss or parasite gain? Story of Contracaecum nematodes in antipodean waters. Parasite Epidemiology Control, 4, e00087. https://doi.org/10.1016/ j.parepi. 2019.e00087 DOI: https://doi.org/10.1016/j.parepi.2019.e00087
Shamsi, S. (2020). Seafood-borne parasites in Australia: Human health risks, fact or fiction? Microbiology Australia, 41(1), 33- 37. DOI: https://doi.org/10.1071/MA20009
Shamsi, S., & Sheorey, H. (2018). Seafood-borne parasitic diseases in Australia: Are they rare or underdiagnosed? Internal Medicine Journal, 48, 591-596. https://doi. org/10.1111/imj.13786 DOI: https://doi.org/10.1111/imj.13786
Shimamura, Y., Muwanwella, N., Chandran, S., Kandel, G., & Marcon, N. (2016). Common symptoms from an uncommon infection: Gastrointestinal Anisakiasis. Canadian Journal of Gastroenterology and Hepatology, e5176502. https://doi.org/ 10.1155/ 2016/5176502 DOI: https://doi.org/10.1155/2016/5176502
Sonko, P., Chih-Cheng Chen, S., Chou, C. M., Huang, Y. C., Hsu, S. L., Barčák, D., Oros, M., & Fan, C.-K. (2020). Multidisciplinary approach in study of the zoonotic Anisakis larval infection in the blue mackerel (Scomber australasicus) and the largehead hairtail (Trichiurus lepturus) in Northern Taiwan. Journal of Microbiology, Immunology and Infection, 53(6), 1021-1029. https://doi.org/10.1016/j. jmii.2019.04.012 DOI: https://doi.org/10.1016/j.jmii.2019.04.012
Totoiu, A., Nenciu, M.-I., & Nicolae, C. G. (2018). Assessing the inter-relations between fish health and stock status on human health and consumer perception. Scientific Papers, Series D. Animal Science, 61(2), 268-73. https://doi.org/10.1016/j fishres.2017.06.018
Tunya, R., Wongsawad, C., Wongsawad, P., & Chai, J.-Y. (2020). Morphological and molecular characteristics of Anisakis typica larvae in two species of Threadfin Bream, Nemipterus hexodon and Nemipterus japonicus, from the Gulf of Thailand. Korean Journal of Parasitology, 58, 15-25. https://doi.org/10.3347/kjp.2020. 58.1.15 DOI: https://doi.org/10.3347/kjp.2020.58.1.15
Van Hien, H., Thi Dung, B., Ngo, H. D., & Doanh, P. N. (2021). First morphological and molecular identification of third-stage larvae of Anisakis typica (Nematoda: Anisakidae) from marine fishes in Vietnamese water. Journal of Nematology, 53, e2021-10. https://doi.org/10.21307/ jofnem-2021-01 DOI: https://doi.org/10.21307/jofnem-2021-010
Zamora, V., Carlos, Andreu-Ballester, J., Rodero, M., & Cuéllar, C. (2021). Anisakis simplex: Immunomodulatory effects of larval antigens on the activation of toll like receptors. Journal of International Immunopharmacology, 100, 108120. https:// doi.org/10.1016/j.intimp.2021.108120 DOI: https://doi.org/10.1016/j.intimp.2021.108120
Additional Files
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Universiti Malaysia Terengganu Journal of Undergraduate Research
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.