Abstract
The aim of the present study was to conduct, in southern Australian waters, a preliminary epidemiological survey of five commercially significant species of fish (yellow-eye mullet, tiger flathead, sand flathead, pilchard and king fish) for infections with anisakid nematodes larvae using a combined morphological–molecular approach. With the exception of king fish, which was farmed and fed commercial pellets, all other species were infected with at least one species of anisakid nematode, with each individual tiger flathead examined being infected. Five morphotypes, including Anisakis, Contracaecum type I and II and Hysterothylacium type IV and VIII, were defined genetically using mutation scanning and targeted sequencing of the second internal transcribed spacer of nuclear ribosomal DNA. The findings of the present study provide a basis for future investigations of the genetic composition of anisakid populations in a wide range of fish hosts in Australia and for assessing their public health significance.
Similar content being viewed by others
References
Angot V, Brasseur P (1995) Les larves d’anisakides et leur incidence sur la qualite des poissons et produits de poisson. Rev Med Vet 146:791–804
Audicana MT, Kennedy MW (2008) Anisakis simplex: from obscure infectious worm to inducer of immune hypersensitivity. Clin Microbiol Rev 21(2):360–379
Audicana MT, Ansotegui IJ, Fernandez de Corres L, Kennedy MW (2002) Anisakis simplex: dangerous—dead and alive? Trends in Parasitology. Trends Parasitol 18:20–25
Beumer JP, Ashburner LD, Burbury ME, Jette E, Latham DJ (1982) A checklist of the parasites of fishes from Australia and its adjacent Antarctic territories. Commonwealth Agricultural Bureaux, Technical Communication No. 48 of the Commonwealth Institute of Parasitology
Bruce NL (1990a) Hysterothylacium Ward and Magath, 1917, and Ichthyascaris Wu, 1949, ascaridoid nematodes from Australian demersal fishes. Mem Queensl Mus 28:389–426
Bruce NL (1990b) Redescription of the Ascaridoid nematode Hysterothylacium scomberomori (Yamaguti) from Australian Spanish mackerel Scomberomorus commerson (Lacepede). Mem Queensl Mus 28:427–434
Bruce NL, Cannon LRG (1989) Hysterothylacium, Iheringascaris and Maricostula new genus, nematodes (Ascaridoidea) from Australian pelagic marine fishes. J Nat Hist 23:1397–1441
Bruce NL, Cannon LRG (1990) Ascaridoid nematodes from sharks from Australia and the Solomon Islands, southwestern Pacific Ocean. Invertebr Syst 4:763–783
Bruce NL, Adlard RD, Cannon LRG (1994) Synoptic checklist of ascaridoid parasites (Nematoda) from fish hosts. Invertebr Taxon 8:583–674
Burt MDB, Campbell JD, Likely CG, Smith JW (1990) Serial passage of larval Pseudoterranova decipiens (Nematoda: Ascaridoidea) in fish. Can J Fish Aquat Sci 47:693–695
Cannon LRG (1977) Some larval ascaridoids from south-eastern Queensland marine fishes. Int J Parasitol 7:233–243
Chai J, Murrell KD, Lymbery AJ (2005) Fish-borne parasitic zoonoses: status and issues. Int J Parasitol 35:1233–1254
D’Amelio S (2003) Phylogeny of anisakid nematodes: a review. Helminthologia 40:87–91
D’Amelio S, Mathiopoulos KD, Brandonisio O, Lucarelli G, Doronzo F, Paggi L (1999) Diagnosis of a case of gastric anisakidosis by PCR-based restriction fragment length polymorphism analysis. Parassitologia (Roma) 41:591–593
Deardorff TL, Overstreet RM (1981) Larval Hysterothylacium (=Thynnascaris) (Nematoda: Anisakidae) from fishes and invertebrates in the Gulf of Mexico. Proc Helminthol Soc Wash 48:113–126
De Corres LF et al (1996) Anisakis simplex induces not only anisakiasis: report on 28 cases of allergy caused by this nematode. J Investig Allergol Clin Immunol 6:315–319
Dei-Cas E et al (1986) Human anisakiasis. Five new cases in the northern France. Gastroenterol Clin Biol 10:83–87
Doupe RG, Lymbery AJ, Wong S, Hobbs RP (2003) Larval anisakid infections of some tropical fish species from north-west Australia. J Helminthol 77:363–365
Fagerholm HP (1988) Incubation in rats of a nematodal larva from cod to establish its specific identity: Contracaecum osculatum, (Rudolphi). Parasitol Res 75:57–63
Fagerholm HP (1991) Systematic implications of male caudal morphology in ascaridoid nematode parasites. Syst Parasitol 19:215–228
Gasser RB et al (2006) Single-strand conformation polymorphism (SSCP) for the analysis of genetic variation. Nat Protoc 1(6):3121–3128
Gorokhov VV, Sergiev VP, Romanenko NA (1999) Anisakiasis as a growing ecological and social problem. Med Parazitol (Mosk) (4):50–54
Hartwich G (1974) Keys to genera of the Ascaridoidea. In: Anderson RC, Chabaud AG, Willmott S (eds) CIH keys to the nematode parasites of vertebrates. Commonwealth Agricultural Bureaux, Bucks, pp 1–15
Hurst RJ (1984) Identification and description of larval Anisakis simplex and Pseudoterranova decipiens (Anisakidae: Nematoda) from New Zealand waters. NZ J Mar Freshw Res 18:177–186
Hutson KS, Ernst I, Whittington ID (2007) Risk assessment for metazoan parasites of yellowtail kingfish Seriola lalandi (Perciformes: Carangidae) in South Australian sea-cage aquaculture. Aquaculture 271:85–99
Im K, Shin H, Kim B, Moon S (1995) Gastric anisakiasis cases in Cheju-do, Korea Republic. Korean J Parasitol 33:179–186
Jensen T (1997) Experimental infection/transmission of sculpins (Myoxocephalus scorpius) and cod (Gadus morhua) by sealworm (Pseudoterranova decipiens) larvae. Parasitol Res 83:380–382
Kagei N et al (1995) A case of hepatic anisakiasis with a literal survey for extra-intestinal anisakiasis. Jpn J Parasitol 44:346–351
Lebedev BI (1968) Helminth fauna of carangid fish in the Pacific Ocean. Soobshch. Dal’nevost. Fil. V. L. Komarova sib. Otdel. Akad. Nauk SSSR 26:80–85
Li A et al (2005) Genetic evidence for the existence of sibling species within Contracaecum rudolphii (Hartwich, 1964) and the validity of Contracaecum septentrionale (Kreis, 1955) (Nematoda: Anisakidae). Parasitol Res 96:361–366
Lopata AL, Lehrer SB (2009) New insights into seafood allergy. Curr Opin Allergy Clin Immunol 9:270–277
Marques JF, Cabral HN, Busi M, D’Amelio S (2006) Molecular identification of Anisakis species from Pleuronectiformes off the Portuguese coast. J Helminthol 80:47–51
Mawson PM, Angel M, Edmonds SJ (1986) A checklist of helminths from Australian birds. Rec South Aust Mus 19:219–325
Moreno-Ancillo A, Caballero MT, Cabanas R (1997) Allergic reactions to Anisakis simplex parasitizing seafood. Ann Allergy Asthma Immunol 79:246–250
Oshima T (1972) Anisakis and Anisakiasis in Japan and adjacent area. In: Progress of medical parasitology in Japan, pp 301–393
Shamsi S, Gasser R, Beveridge I, Shabani AA (2008) A description of C. multipapillatum (von Drasche, 1882) from the Australian pelican, Pelecanus conspicillatus. Parasitol Res 103:1031–1039
Shamsi S, Norman R, Gasser R, Beveridge I (2009a) Genetic and morphological evidences for the existence of sibling species within Contracaecum rudolphii (Hartwich, 1964) (Nematoda: Anisakidae) in Australia. Parasitol Res 105:529–538
Shamsi S, Norman R, Gasser R, Beveridge I (2009b) Redescription and genetic characterization of selected Contracaecum spp. (Nematoda: Anisakidae) from various hosts in Australia. Parasitol Res 104:1507–1525
Smith JW, Wootten R (1978) Anisakis and anisakiasis. Adv Parasitol 16:93–163
Speare P (1999) Parasites from east coast Australian billfish. Mem Queensl Mus 43:837–848
Strmnes E, Andersen K (2000) “Spring rise” of whaleworm (Anisakis simplex; Nematoda, Ascaridoidea) third-stage larvae in some fish species from Norwegian waters. Parasitol Res 86:619–624
Takahashi S, Ishikura H, Kikuchi K (1998) Anisakidosis: global point of view. In: Ishikura H, Aikawa M, Itakura H, Kikuchi K (eds) Host response to international parasitic zoonoses. Springer-verlag, Tokyo, pp 109–120
Thompson RCA (1982) Intraspecific variation and parasite epidemiology. In: Parasites—their world and ours. Proceedings of the 5th International Congress of Parasitology, Toronto, Canada, 7–14 August, 1982, under the auspices of the World Federation of Parasitologists. Elsevier Biomedical Press, Amsterdam Netherlands, pp 369–378
Thompson JD, Gibson TJ, Plewniac F, Jeanmougin F, Higgins DG (1997) The ClustalX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 24:4876–4882
Van Thiel PH, Kuipers FC, Roskam RT (1960) A nematode parasitic to herring, causing acute abdominal syndromes in man. Trop Geogr Med 2:97–113
Woo PTK (1995) Fish diseases and disorders volume 1: protozoan and metazoan infections. In: Fish diseases and disorders volume 1: protozoan and metazoan infections. CAB International, Wallingford, UK
Yagi K, Nagasawa K, Ishikura H, Nakagawa A, Sato N, Kikuchi K, Ishikura H (1996) Female worm Hysterothylacium aduncum excreted from human: a case report. Jpn J Parasitol 45:12–23
Yoshinaga T, Kinami R, Hall KA, Ogawa K (2006) A preliminary study on the infection of anisakid larvae in juvenile greater amberjack Seriola dumerili imported from China to Japan as mariculture seedlings. Fish Pathology (Gyobyo Kenkyu) 41:123–126
Zhang L et al (2007) 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 21:386–390
Acknowledgements
This study was financially supported by the Australian Biological Resources Study (ABRS), Australia.
Author information
Authors and Affiliations
Corresponding author
Additional information
Nucleotide sequence data reported in this paper are available in the GenBank database under the accession numbers FN556176 to FN556182.
Rights and permissions
About this article
Cite this article
Shamsi, S., Eisenbarth, A., Saptarshi, S. et al. Occurrence and abundance of anisakid nematode larvae in five species of fish from southern Australian waters. Parasitol Res 108, 927–934 (2011). https://doi.org/10.1007/s00436-010-2134-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00436-010-2134-1