Home A case of persisting massive infection of Scomberomorus commerson, a commercially exploited scombrid fish, with Cybicola armatus (Copepoda: Siphonostomatoida: Pseudocycnidae)
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A case of persisting massive infection of Scomberomorus commerson, a commercially exploited scombrid fish, with Cybicola armatus (Copepoda: Siphonostomatoida: Pseudocycnidae)

  • Ameri Kottarathil Helna , Kappalli Sudha EMAIL logo , Panakkool Thamban Aneesh , Wojciech Piasecki and Gopinathan Anilkumar
Published/Copyright: October 24, 2016
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Abstract

During an extensive survey of fish parasites along the Malabar coast of India we observed exceptionally high or even massive infection of the narrow-barred Spanish mackerel, Scomberomorus commerson (Scombridae), with parasitic copepods Cybicola armatus. Such infection has not hitherto been reported. The copepods occurred on the gills of its host and the infection persisted for many years (the survey lasted from January 2010 to July 2014). The overall prevalence was very high (95%); out of a total of 981 fish studied, 933 were infected, and the maximum intensity reached 42. The highest rate of infection (prevalence 99.2%) was observed in medium sized fish (36.0-79.9 cm). We found this parasite only on S. commerson even though we examined 81 fish species, including five of the family Scombridae. Interestingly, the parasite exhibits strict site specificity and microhabitat preference. A significant proportion of them was seen attached to pseudobranchs rather than to main gill arches. Significantly, the body size of the parasite was positively correlated with that of the host fish. Our SEM micrographs contributed new facts to this copepod’s morphology by illustrating for the first time the ventral part of its cephalothorax, illustrating the nature of attachment, and by finding a new structure – a premaxillary pad. We demonstrated the haematophagous nature of C. armatus by finding and documenting the host’s blood cells in the parasite’s intestine.

Acknowledgements

The authors gratefully acknowledge Kerala State Council for Science Technology and Environment, Government of Kerala (No. (T) 093/SRS/2011/CSTE, dated 25/06/2011) and University Grants Commission, New Delhi (Order No. F. No. 38218/2009 (SR) dated 24/12/2009) for financial support to carry out this work.

References

Abdel-Aal A.A., Soliman M.F. 2004. Microhabitat and surface ultrastructure of Neothoracocotyle commersoni and Priceamultae (Monogenea: Microcotyloidea) from gills of scombrid fish, Scomberomorus commerson. Journal of the Egyptian Society of Parasitology, 34, 117–130Search in Google Scholar

Abdul Khalid N.Q., Shaharoum-Harrison F. 2014. The life cycle of the parasitic crustacean, Lernanthropus latis Yamaguti, 1954 (Copepoda: Lernanthropidae), on marine-cultured fish, Lates calcarifer, from Setiu Wetland, Terengganu. Journal of Parasitology Research, 697134, 6 pages. 10.1155/2014/697134Search in Google Scholar PubMed PubMed Central

Adel M., Azizi H.R., Nematolahi A. 2013. Scomberomorus commerson, a new paratenic host of Contracaecum sp. and Anisakis sp. (Nematoda: Anisakidae) from Persian Gulf. World Journal of Fish and Marine Sciences, 5, 310–314Search in Google Scholar

Adlard R.D., Bryant M.S., Whipps C.M., Kent M.L. 2005 Multivalvulid myxozoans from eastern Australia: Three new species of Kudoa from scombrid and labrid fishes of the Great Barrier Reef, Queensland, Australia. Journal of Parasitology, 91, 1138–1142. 10.1645/GE-368R.1Search in Google Scholar PubMed

Aloo P.A., Anam R.O., Mwangi J.N. 2004. Metazoan parasites of some commercially important fish along the Kenyan coast. Western Indian Ocean Journal of Marine Science, 3, 71–78Search in Google Scholar

Aneesh P.T. 2014. Studies on parasitic crustaceans infecting the fishes of Malabar Coast. PhD Thesis, Kannur UniversitySearch in Google Scholar

Arthur J.R., Lumanlan-Mayo S. 1997. Checklist of the parasites of fishes of the Philippines. FAO Fisheries Technical Paper, 369, FAO, Rome. pp. 102Search in Google Scholar

Baker T.G., Pante E., de Buron I. 2005. Co-occurrence of Naobranchia lizae (Copepoda) and Metamicrocotyla macracantha (Monogenea), gill parasites of the striped mullet Mugil cephalus. Parasitology Research, 97, 515–520. 10.1007/ s00436-005-1485-5Search in Google Scholar

Bassett-Smith P.W. 1898a. Some new parasitic copepods found on fish at Bombay. Annals and Magazine of Natural History, 1, 1–1710.1080/00222939808677915Search in Google Scholar

Bassett-Smith P.W. 1898b. Some new or rare parasitic copepods found on fish in the Indo-tropic region. Annals and Magazine of Natural History, 11, 359–37210.1080/00222939808678056Search in Google Scholar

Beveridge I., Bray R.A., Cribb T.H., Justine J.-L. 2014. Diversity of trypanorhynch metacestodes in teleost fishes from coral reefs off eastern Australia and New Caledonia. Parasite 21, 60. 10.1051/parasite/2014060Search in Google Scholar PubMed PubMed Central

Boxshall G.A. 2005. Copepods. In: Rohde K. (Ed.), Marine Parasites. CSIRO Publishing, Collingwood, Vic., Australia, pp.123-138Search in Google Scholar

Boxshall G.A., Halsey S.H. 2004. An introduction to copepod diversity. Ray Society, London. No. 166, pp. 966Search in Google Scholar

Bray R.A., Cribb T.H., Barker S.C. 1993. Hemiuridae (Digenea) from marine fishes of the Great Barrier Reef, Queensland, Australia. Systematic Parasitology, 25, 37–62.10.1007/BF00017000Search in Google Scholar

Bruce N.L. 1990. Redescription of the ascaridoid nematode Hysterothylacium scomberomori (Yamaguti) from Australian Spanish mackerel Scomberomorus commerson (Lacepède). Memoirs of the Queensland Museum, 28, 427–434Search in Google Scholar

Bush A.O., Lafferty K.D., Lotz J.M., Shostak A.W. 1997. Parasitology meets ecology on its own terms. Margolis et al. revisited. Journal of Parasitology, 83, 575–583. 10.2307/3284227Search in Google Scholar

Cabral P., Coste F., RaibautA. 1984. Cycle évolutif de Lernanthropus kroyerii Van Beneden, 1851, Copépode branchial hématophage du loup Dicentrarchus labrax (Linné, 1758) dans des populations naturelles et en élevage. Annales de Parasitologie Humaine et Comparee, 59, 189–207 (In French)10.1051/parasite/1984592189Search in Google Scholar PubMed

Castro R., Santos M.J. 2013. Metazoan ectoparasites of Atlantic mackerel, Scomber scombrus (Teleostei: Scombridae): macroand microhabitat distribution. Parasitology Research, 112, 3579–3586. 10.1007/s00436-013-3543-8Search in Google Scholar PubMed

Cavaleiro F.I., Santos M.J. 2011. Site selection of Acanthochondria cornuta (Copepoda: Chondracanthidae) in Platichthys flesus (Teleostei: Pleuronectidae). Parasitology, 138, 1061–1067. 10.1017/S1368980008002541Search in Google Scholar

Cressey R.F., Cressey H.B. 1979. The parasitic copepods of Indo-West Pacific lizardfishes (Synodontidae). Smithsonian Contributions to Zoology, 196, 1–71. 10.5479/si.00810282.296Search in Google Scholar

Cressey R.F., Cressey H.B. 1980. The parasitic copepods of mackerel and tuna-like fishes (Scombridae) of the world. Smithsonian Contributions to Zoology, 311, 1–186. 10.5479/si.00 810282.311.iSearch in Google Scholar

Cressey R.F., Collette B.B., Russo L. 1983. Copepods and scombrid fishes: A study in host-parasite relationships. Fishery Bulletin, 81, 227–265Search in Google Scholar

deMeeûs T., Marin R., Renaud F. 1992. Genetic heterogeneity within populations of Lepeophtheirus europaensis (Copepoda, Caligidae) parasite on to host species. International Journal of Parasitology, 8, 1179–1181. 10.1016/0020-7519(92) 90039-NSearch in Google Scholar

Froese R., Pauly D. 2016. FishBase. World Wide Web electronic publication. Available from: http://www.Fishbase.org, Version (January 2016). Accessed 4 July 2016.Search in Google Scholar

Gnanamuthu C.P. 1950. Two dichelesthiid copepods from Madras fish. Parasitology, 40, 276–282. 10.1017/S0031182000018138Search in Google Scholar

Heegaard P.E. 1962. Parasitic Copepoda from Australian waters. Records of the Australian Museum, 25, 149–23410.3853/j.0067-1975.25.1962.661Search in Google Scholar

Hermida M., Cruz C., Saraiva A. 2012. Distribution of Hatschekia pagellibogneravei (Copepoda: Hatschekiidae) on the gills of Pagellus bogaraveo (Teleostei: Sparidae) from Madeira, Portugal. FoliaParasitologica, 59, 148–152. 10.14411/fp.2012.020Search in Google Scholar

Huys R., Boxshall G.A. 1991. Copepod evolution. Ray Society, London. No. 159, pp. 468Search in Google Scholar

Johnson S.C., Treasurer J.W., Bravo S., Nagasawa K., Kabata Z. 2004. A review of the impact of parasitic copepods on marine aquaculture. Zoological Studies, 43, 229–243Search in Google Scholar

Kabata Z. 1979. Parasitic Copepoda of British fishes. Ray Society, London. No. 152, pp. 468Search in Google Scholar

Kabata Z. 1982. Copepoda (Crustacea) parasitic on fishes: Problems and perspectives. Advances in Parasitology, 19, 1–71. 10.1016/S0065-308X(08)60265-1Search in Google Scholar

Kensley B., Grindley J.R. 1973. South African parasitic Copepoda. Annals of the South African Museum, 62, 69–13010.1080/02580144.1973.10429225Search in Google Scholar

Kirtisinghe P. 1935. Parasitic copepods of fish from Ceylon. Para-sitology, 27, 332–344. 10.1017/S0031182000015249Search in Google Scholar

Kirtisinghe P. 1937. On the genus Cybicola Basett-Smith (1898). Par-asitology, 29, 453–456. 10.1017/S0031182000024987Search in Google Scholar

Kirtisinghe P. 1964. A review of the parasitic copepods of fish recorded from Ceylon with description of additional forms. Bulletin ofthe Fisheries Research Station, Ceylon 17, 45–132Search in Google Scholar

Kurian C.V. 1965. Parasitic copepods of fishes from Kerala – No. 3. Bulletin of the Research Institute, University ofKerala, 8, 63–66Search in Google Scholar

Lester R.J.G., Thompson C., Moss H., Barker S.C. 2001. Movement and stock structure of narrow-barred Spanish mackerel as indicated by parasites. Journal of Fish Biology, 59, 833–842. 10.1111/j.1095-8649.2001.tb00154.xSearch in Google Scholar

Lin C.L., Ho J.S. 2006. Four species of Unicolax Cressey and Cressey, 1980 (Copepoda: Bomolochidae) parasitic on marine fishes of Taiwan. Zoological Studies, 45, 339–356Search in Google Scholar

Lo C.M., Morand S. 2001. Gill parasites of Cephalopholis argus (Teleostei: Serranidae) from Morrea (French Polynesia): Site selection and coexistence. Folia Parasitologica, 48, 30–36. 10.14411/fp.2001.006Search in Google Scholar

Mattiucci S., Paggi L., Nascetti G., Portes Santos C., Costa G., Di Beneditto A.P., Ramos R., Argyrou M., Cianchi R., Bullini L. 2002. Genetic markers in the study of Anisakis typica (Diesing, 1860): larval identification and genetic relationships with other species of Anisakis Dujardin, 1845 (Nematoda: Anisakidae). Systematic Parasitology, 51, 159–17010.1023/A:1014554900808Search in Google Scholar

Moore B.R., Buckworth R.C., Moss H., Lester R.J.G. 2003. Stock discrimination and movements of narrow-barred Spanish mackerel across northern Australia as indicated by parasites. Journal of Fish Biology, 63, 765–779. 10.1046/j.1095- 8649.2003.00190.xSearch in Google Scholar

Morton A.B., Routledge R. 2005. Mortality rates for juvenile pink Oncorhynchus gorbuscha and chum O. keta salmon infested with sea lice Lepeophtheirus salmonis in the Broughton Ar-chipelago. Alaska Fishery Research Bulletin 11, 146–152Search in Google Scholar

Natarajan P., Balakrishnan Nair N. 1972. Observations on Pseudocycnus armatus (Bassett-Smith) parasitic on Indocybium guttatum (Bloch and Schn.). Hydrobiologia, 40, 69–76. 10.1007/BF00123593Search in Google Scholar

Nolan M.J., Cribb T.H. 2006. Cardicola Short, 1953 and Braya n. gen. (Digenea: Sanguinicolidae) from five families of tropical Indo-Pacific fishes. Zootaxa, 1265, 1–8010.11646/zootaxa.1265.1.1Search in Google Scholar

Piasecki W. 1989. Life cycle of Tracheliastes maculatus Kollar, 1835 (Copepoda, Siphonostomatoida, Lernaeopodidae). Wiadomosci Parazytologiczne, 35, 187–245Search in Google Scholar

Piasecki W. 1994. Infection seasonality of Tracheliastes maculatus Kollar, 1835 (Copepoda, Siphonostomatoida, Lernaeopodidae) in the warm-water canal of the “Dolna Odra” power plant. Wiadomosci Parazytologiczne, 40, 187–192Search in Google Scholar

Piasecki W., Avenant-Oldewage A. 2008. Diseases caused by Crustacea. pp. 1113–1198. In: Eiras J., Segner H., Wahli T., Kapoor B.G. (Eds.) Fish diseases. Science Publishers, Enfield, NH, USA, pp. 1200Search in Google Scholar

Piasecki W., Goodwin A.E., Eiras J.C., Nowak B.F. 2004. Importance of Copepoda in freshwater aquaculture. Zoological Studies, 43, 193–205Search in Google Scholar

Piasecki W., MacKinnon B.M. 1995. Life cycle of a sea louse, Caligus elongatus von Nordmann, 1832 (Copepoda, Siphonostomatoida, Caligidae). Canadian Journal of Zoology, 73, 74–82. 10.1139/z95-009Search in Google Scholar

Pillai N.K. 1964. A miscellaneous collection of copepods parasitic on South Indian fishes. Journal of the Marine Biological Association of India, 6, 61–83Search in Google Scholar

Pillai N.K. 1985. The fauna of India: Copepod parasites of marine fishes. Zoological Survey of India, Calcutta, pp. 900Search in Google Scholar

Ramasamy P., Ramalinga M.K., Hanna R.E.B., Halton D.W. 1985. Microhabitats of gill parasites (Monogenea and Copepoda) of teleosts (Scomberoides spp.). International Journal of Parasitology, 15, 385–397. 10.1016/0020-7519(85)90023-2Search in Google Scholar

Rohde K. 1980. Host specificity indices of parasites and their application. Experientia, 36, 1369–1371. 10.1007/BF01960103Search in Google Scholar

Rohde K. 1993. Ecology of marine parasites, 2nd edn. CAB International, Wallingford, pp. 29810.1079/9780851988450.0000Search in Google Scholar

Rohde K. 1994. Niche restriction in parasites: proximate and ultimate causes. Parasitology, 109: S69-S84. 10.1017/ s0031182000085097Search in Google Scholar

Samotylova N.N. 2011. Representatives of Cyclopoida and Siphonostomatoida (Crustacea: Copepoda) in Vietnamese fauna. Izvestja Samarskogo nauchnogo centra Rosijskoj akademii nauk, 13, 1146–1148. (In Russian)Search in Google Scholar

Scott-Holland T.B., Bennett S.M., Bennett M.B. 2006. Distribution of an asymmetrical copepod, Hatschekia plectropomi, on the gills of Plectropomus leopardus. Journal of Fish Biology, 68, 222–235. 10.1111/j.0022-1112.2006.00895.x.Search in Google Scholar

Sethi S. 2012. Occurence [sic] of parasitic copepods, Lernaeenicus sprattae on king mackerel (Scomberomorus commerson), along south-east of India. e-planet 10, 36–38Search in Google Scholar

Shaharom F.M., Lester R.J.G. 1982. Description of and observations on Grillotia branchi n.sp., a larval trypanorhynch from the branchial arches of the Spanish mackerel, Scomberomorus commerson. Systematic Parasitology, 4, 1–6. 10.1007/BF00012227Search in Google Scholar

Shinn A.P., Pratoomyot J., Bron J.E., Paladini G., Brooker E.E., Brooker A.J. 2015. Economic costs of protistan and metazoan parasites to global mariculture. Parasitology, 142, si1, 196270. 10.1017/S0031182014001437Search in Google Scholar

Silas E.G., Ummerkutty A.N.P. 1967. Parasites of scombroid fishes. Part II. Parasitic Copepoda. Proceedings of the Symposium on scombroid fishes held at Mandapam Camp from January 12–15, 1962. Part III. Symposium Series I, Marine Biological Association of India, Mandapam Camp, S. India, pp. 876–993Search in Google Scholar

Sasidharan Pillai N.K. 1984. Studies on the copepod fish parasites of Kerala coast. PhD Thesis. Department of Industrial Fisheries, University of Cochin, Cohin, IndiaSearch in Google Scholar

Székely C., Láng M., Molnár K. 2010. Role of the copepod parasite Tracheliastes maculatus Kollar, 1836 (Lernaeopodidae) in the common bream (Abramis brama) mortality occurring in Lake Balaton, Hungary. Bulletin of the European Association of Fish Pathologists, 30, 170–176Search in Google Scholar

Whipps C.M., Adlard R.D., Bryant M.S., Kent M.L. 2003. Two unusual myxozoans, Kudoa quadricornis n. sp. (Multivalvulida) from the muscle of goldspotted trevally (Carangoides fulvoguttatus) and Kudoa permulticapsula n. sp. (Multivalvulida) from the muscle of Spanish mackerel (Scomberomorus commerson) from the Great Barrier Reef, Australia. Journal of Parasitology, 89, 168–173. 10.1645/0022-3395 (2003)089[0168:TUMKQN]2.0.CO;2Search in Google Scholar

Williams R.E., Lester R.J.G. 2006. Stock structure of Spanish mackerel Scomberomorus commerson along the Australian east coast deduced from parasite data. Journal of Fish Biology, 68, 1707–1712. 10.1111/j.1095-8649.2006.01026.xSearch in Google Scholar

Wilson C.B. 1922. North American parasitic copepods belonging to the family Dichelesthiidae. Proceedings of the United States National Museum, 60, 1–9810.5479/si.00963801.60-2400.1Search in Google Scholar

Wilson J.M., Laurent P. 2002. Fish gill morphology: Inside out. Journal of Experimental Zoology, 293, 192–213. 10.1002/jez.10124Search in Google Scholar

Yamaguti S.(Ed.) 1963. Parasitic Copepoda and Branchiura of fishes. Interscience Publishers, New York, pp. 1104Search in Google Scholar

Received: 2015-10-16
Revised: 2016-7-15
Accepted: 2016-8-3
Published Online: 2016-10-24
Published in Print: 2016-12-1

© 2016 W. Stefañski Institute of Parasitology, PAS

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