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The life cycle of Hexangium sigani Goto & Ozaki, 1929 (Digenea: Microscaphidiidae) from the Red Sea

Published online by Cambridge University Press:  17 August 2015

R.M. El-Said Hassanine*
Affiliation:
Biological Sciences Department, Rabigh-Faculty of Science and Arts, King Abdulaziz University, PO Box 344, Rabigh21911, Saudi Arabia Department of Zoology, New Valley-Faculty of Science, Assiut University, El-Kharga, New Valley, Egypt
D.A. Al-Zahrani
Affiliation:
Biological Sciences Department, Rabigh-Faculty of Science and Arts, King Abdulaziz University, PO Box 344, Rabigh21911, Saudi Arabia
H. El-S. Touliabah
Affiliation:
Biological Sciences Department, Rabigh-Faculty of Science and Arts, King Abdulaziz University, PO Box 344, Rabigh21911, Saudi Arabia
E.M. Youssef
Affiliation:
Department of Parasitology, Faculty of Veterinary Medicine, Suez Canal University, Egypt
*

Abstract

The microscaphidiid Hexangium sigani Goto & Ozaki, 1929 was found in the intestine of Siganus rivulatus, a siganid fish permanently resident in a lagoon within the mangrove swamps on the Egyptian coast of the Gulf of Aqaba. Intra-molluscan stages of this trematode (mother sporocysts, rediae and cercariae) were found in the gonads and digestive gland of Nassarius pullus (Gastropoda: Nassariidae), a common snail in the same lagoon. Consequently, the life cycle of H. sigani was elucidated under natural conditions: eggs are directly ingested by the snail; mother sporocysts and rediae reach maturity 5–7 and 16–17 weeks post-infection; rediae contain 18–26 developing cercariae; fully developed cercariae are monostome, without penetration glands, emerge from the snail during the night 18–19 weeks post-infection and rapidly encyst on aquatic vegetation (there is no second intermediate host); encysted metacercariae are not progenetic; 2-day-old metacercariae encysted on filamentous algae fed to S. rivulatus developed into fully mature worms 5–6 weeks post-infection. The cycle was completed in about 24 weeks. The intra-molluscan stages are very similar to those of Dictyangium chelydrae Stunkard, 1943, the only described intra-molluscan stages of any microscaphidiid. However, they are also similar to those of the family Mesometridae. The present study of H. sigani describes the first complete microscaphidiid life cycle, and implicitly supports the phylogenetic relationship of this family with the Mesometridae inferred from molecular phylogenetic studies.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2015 

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References

Al-Jahdali, M.O. (2013) New intestinal trematodes from siganid fishes off the Saudi coast of the Red Sea. Acta Zoologica Academiae Scientiarum Hungaricae 59, 312.Google Scholar
Al-Yamani, F.Y. & Nahhas, F.M. (1981) Digenetic trematodes of marine fishes from the Kuwaiti coast of the Arabian Gulf. Kuwait Bulletin of Marine Science 3, 122.Google Scholar
Blair, D. (2005) Family Microscaphidiidae Looss, 1900. pp. 189192 in Gibson, D.I., Jones, A. & Bray, R.A. (Eds) Keys to the Trematoda. Vol.2. Wallingford, CABI Publishing.Google Scholar
Bozhkov, D.K. (1982) Helminths. Life cycle and their evolution. pp. 1117. Sofia, Nauka i Izkustvo.Google Scholar
Bray, R.A., Waeschenbach, A., Cribb, T.H., Weedall, G.D., Dyal, P. & Littlewood, D.T.J. (2009) The phylogeny of the Lepocreadioidea (Platyhelminthes, Digenea) inferred from nuclear and mitochondrial genes: implications for their systematics and evolution. Acta Parasitologica 54, 310329.Google Scholar
Brooks, D.R., O'Grady, R.T. & Glen, D.R. (1985) Phylogenetic analysis of the Digenea (Platyhelminthes, Cercomeria) with comments on their adaptative radiation. Canadian Journal of Zoology 63, 411443.Google Scholar
Cribb, T.H., Bray, R.A., Olson, P.D. & Littlewood, D.T.J. (2003) Life cycle evolution in the Digenea: a new perspective from phylogeny. Advances in Parasitology 54, 198254.Google Scholar
Dzikowski, R., Paperna, I. & Diamant, A. (2003) Multi-annual changes in the parasite communities of rabbitfish Siganus rivulatus (Siganidae) in the Gulf of Aqaba, Red Sea. Helgoland Marine Research 57, 228235.Google Scholar
El-Labadi, S., Ismail, S. & Khalaf, M. (2006) Intestinal digenetic trematodes of some fishes from the Gulf of Aqaba, Red Sea. Pakistan Journal of Zoology 38, 4348.Google Scholar
Fischthal, J.H. & Kuntz, R.E. (1964) Digenetic trematodes of fishes from Palawan Island, Philippines. I. Families: Acanthocolpidae, Angiodictyidae, Cryptogonimidae, Fellodistomidae and Gyliauchenidae. Journal of Parasitology 50, 248252.Google Scholar
Fischthal, J.H. & Kuntz, R.E. (1965) Digenetic trematodes of fishes from North Borneo (Malaysia). Proceedings of the Helminthological Society of Washington 32, 6371.Google Scholar
Froese, R. & Pauly, D. (2014) FishBase World Wide Web electronic publication, available at www.fishbase.org , version 04/2014 (accessed March 2014).Google Scholar
Geets, A. & Ollevier, F. (1996) Endoparasitic helminthes of the whitespotted rabbitfish (Siganus sutor Valenciennes, 1835) off the Kenyan coast: distribution within the host population and microhabitat use. Belgian Journal of Zoology 126, 2136.Google Scholar
Gibson, D.I. (1987) Questions in digenean systematic and evolution. Parasitology 95, 429460.Google Scholar
Hassanine, R.M. & Gibson, D.I. (2005) Trematodes of Red Sea fishes: Hexangium brayi n. sp. (Angiodictyidae Looss, 1902) and Siphodera aegyptensis n. sp. (Cryptogonimidae Ward, 1917), with a review of their genera. Systematic Parasitology 61, 215222.CrossRefGoogle Scholar
Jousson, O. & Bartoli, P. (1999) The life-cycle of three species of the Mesometridae (Digenea) with comments on the taxonomic status of this family. Systematic Parasitology 44, 217228.Google Scholar
Jousson, O., Bartoli, P., Zaninetti, L. & Pawlowski, J. (1998) Use of the ITS rDNA for elucidation of some life-cycles of Mesometridae (Trematoda, Digenea). International Journal for Parasitology 28, 14031411.Google Scholar
Kardousha, M.M. (2003) Redescription of ten species of digenetic trematodes from marine fishes of the Emirati coasts of the Arabian Gulf. Arab Gulf Journal of Scientific Research 21, 217226.Google Scholar
Lotz, J.M. & Corkum, C.K. (1984) Notes on the life cycle of Dictyangium chelydrae (Digenea: Microscaphidiidae). Proceedings of the Helminthological Society of Washington 51, 353355.Google Scholar
Martens, E. & Moens, J. (1995) The metazoan ecto- and endoparasites of the rabbitfish, Siganus sutor (Cuvier & Valenciennes, 1835) of the Kenyan coast. I. African Journal of Ecology 33, 405416.Google Scholar
Olson, P.D., Cribb, T.H., Tkach, V.V., Bray, R.A. & Littlewood, D.T.J. (2003) Phylogeny and classification of the Digenea (Platyhelminthes: Trematoda). International Journal for Parasitology 33, 733755.CrossRefGoogle ScholarPubMed
Randall, J.E. (1983) Red Sea reef fishes. 2nd edn. 192 pp. London, IMMEL Publishing.Google Scholar
Sey, O., Nahhas, F.M., Uch, S. & Vang, C. (2003) Digenetic trematodes from marine fishes off the coast of Kuwait, Arabian Gulf: Fellodistomidae and some smaller families, new host and geographical records. Acta Zoologica Academiae Scientiarum Hungaricae 49, 179200.Google Scholar
Sharabati, D. (1984) Red Sea shells. 2nd edn. 128 pp. London, KPI Ltd.Google Scholar
Shen, J.W. (1990) Digenetic trematodes of marine fishes from Hainan Island. 228 pp. Beijing, Science Press (in Chinese).Google Scholar
Tkach, V.V. & Snyder, S.D. (2006) Doodytrema carettochelydis n. gen., n. sp. (Digenea: Microscaphidiidae) from the pig-nosed turtle, Carettochelys insculpta (Cryptodira: Carettochelydidae) in Australia. Comparative Parasitology 73, 165171.Google Scholar
Velasquez, C.C. (1961) Some digenetic trematodes of Philippine food fishes. Journal of Parasitology 47, 521526.Google Scholar