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Endoparasites of three species of house geckoes in Lampung, Indonesia

Published online by Cambridge University Press:  12 April 2024

K. Matsuo*
Affiliation:
Laboratory of Parasitology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan
Y. Oku
Affiliation:
Laboratory of Parasitology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan
*
*Present address and address for correspondence : Department of Parasitology, Hirosaki University School of Medicine, Hirosaki 036-8562, Japan Fax: 81 172 39 5045 Email: kmatsuo@cc.hirosaki-u.ac.jp

Abstract

Thirty-four house geckoes (21 Cosymbotus platyurus, four Gehyra mutilata and nine Hemidactylus frenatus) in December, 1997 (rainy season) and 26 geckos (16 C. platyurus, six G. mutilata and four H. frenatus) in July, 2000 (dry season) were captured in Lampung, Indonesia. Some species of geckoes have been inadvertently introduced to many tropical regions from their native region, but the three species of geckoes in this study are native to Indonesia. Six species of endoparasites were recovered: Oochoristica javanensis (Cestoda) from the small intestine, Paradistomum geckonum (Digenea) from the small intestine and gallbladder, Postorchigenes ovatus (Digenea) from the small intestine, Spauligodon hemidactylus (Nematoda) from the large intestine, and Raillietiella gehyra and R. frenatus (Pentastomida) from the lungs. The prevalence and mean intensity of infection in each species of geckoes are also presented. The prevalence of S. hemidactylus from C. platyurus and H. frenatus in the rainy season was significantly higher than in the dry season. The low prevalence of S. hemidactylus in G. mutilata in the present study corresponded to a previous report from a non-native area. According to the original description, the male of S. hemidactylus lacked a spicule, but in the present study, one male was found with a spicule. The present study suggests male dimorphism occurs in Spauligodon. The number of endoparasite species and snout vent length of geckoes were positively correlated. Geckoes with high worm burdens may be more easily captured by predators.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2002

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References

Ainsworth, R. (1990) Male dimorphism in two new species of nematode (Pharyngodonidae: Oxyurida) from New Zealand lizards. Journal of Parasitology 76, 812822.CrossRefGoogle Scholar
Ali, J.H. & Riley, J. (1983) Experimental life-cycle studies of Raillietiella gehyrae Bovien, 1927 and Raillietiella frenatus Ali, Riley and Self, 1981: pentastomid parasites of geckos utilizing insects as intermediate hosts.. Parasitology 86, 147160.CrossRefGoogle Scholar
Ali, J.H., Riley, J. & Self, J.T. (1981) A revision of the taxonomy of the blunt-hooked Raillietiella, pentastomid parasites of African, South-East-Asian and Indonesian lizards, with a description of a new species. Systematic Parasitology 3, 193207.CrossRefGoogle Scholar
Bursey, C.R. & Goldberg, S.R. (1992) Monthly preva-lences of Spauligodon giganticus (Nematoda Pharyngo-donidae) in naturally infected Yarrow's spiny lizard Sceloporus jarrovii jarrovii (Iguanidae). American Midland Naturalist 127, 204207.CrossRefGoogle Scholar
Bursey, C.R. & Goldberg, S.R. (1996) Spauligodon hemidactylus n. sp. (Nematoda: Pharyngodonidae) from Hemidactylus frenatus (Reptilia: Gekkonidae) from Oceania. Journal of Parasitology 82, 299301.CrossRefGoogle Scholar
Case, T.J., Bolger, D.T. & Petren, K. (1994) Invasions and competitive displacement among house geckos in the tropical Pacific. Ecology 75, 464477.CrossRefGoogle Scholar
Church, G. (1962) The reproductive cycles of the Javanese house geckos, Cosymbotus platyurus, Hemidactylus frenatus, and Peropus mutilatus . Copeia 2, 262269.CrossRefGoogle Scholar
Fisher, R.N. (1997) Dispersal and evolution of the Pacific basin gekkonid lizards Gehyra oceanica and Gehyra mutilata . Evolution 51, 906921.CrossRefGoogle ScholarPubMed
Goldberg, S.R., Bursey, C.R. & Cheam, H. (1998) Gastrointestinal helminths of four gekkonid lizards, Gehyra mutilata, Gehyra oceanica, Hemidactylus frenatus and Lepidodactylus lugubris from the Mariana Islands, Micronesia. Journal of Parasitology 84, 12951298.CrossRefGoogle Scholar
Hasegawa, H. (1985) Helminth parasites of reptiles from Okinawa, Japan. Biology Magazine Okinawa 23, 111.Google Scholar
Kennedy, M.J., Killick, L.M. & Beverley-Burton, M. (1982) Oochoristica javanensis n. sp. (Eucestoda: Linsto-wiidae) from Gehyra mutilata and other geckonid lizards (Lacertila: Geckonidae) from Java, Indonesia.. Canadian Journal of Zoology 60, 24592463.CrossRefGoogle Scholar
Kennedy, M.J., Killick, L.M. & Beverley-Burton, M. (1987a) The prevalence of Paradistomum geckonum, Mesocoelium sociale, and Postorchigenes ovatus (Digenea) in lizards (Suria) from Indonesia. Canadian Journal of Zoology 65, 12921294.CrossRefGoogle Scholar
Kennedy, M.J., Killick, L.M. & Beverley-Burton, M. (1987b) Life cycle studies on two Digenea, Paradistomum geckonum (Diclocoeliidae) and Mesocoelium sociale (Mesocoeliidae), in geckonid lizards from Indonesia. Canadian Journal of Zoology 65, 24912497.CrossRefGoogle Scholar
Lavoipierre, M.M.J. & Rajamanickam, C. (1973) Experimental studies on the life cycle of a lizard pentastomid. Journal of Medical Entomology 10, 301302.CrossRefGoogle ScholarPubMed
Madhavi, R., Nirmala, E. & Subbalakshmi, C. (1998) A population study of the dicrocoeliid trematode Paradistomum orientalis in the garden lizard Calotes versicolor . Journal of Zoology 244, 489496.CrossRefGoogle Scholar
Ota, H. (1994) Female reproductive cycles in the northernmost populations of the two gekkonid lizards, Hemidactylus frenatus and Lepidodactylus lugubris . Ecological Research 9, 121130.CrossRefGoogle Scholar
Petter, A.J. & Quentin, J.C. (1976) Key to the genera of Oxyuroidea. in Anderson, R.C., Chabaud, A.G. & Willmott, S. (Eds) CIH keys to the nematode parasites of vertebrates. 30 pp. Farnham Royal, Bucks, Commonwealth Agricultural Bureaux.Google Scholar
Rendtorff, R.C. (1948) Investigations on the life cycle of Oochoristica and the status of linstowiine cestodes. Journal of Parasitology 34, 243252.CrossRefGoogle Scholar
Riley, J. (1992) Pentastomids and the immune response. Parasitology Today 8, 133137.CrossRefGoogle ScholarPubMed
Welch, K.R.G., Cooke, P.S. & Wright, A.S. (1990) Lizards of the orient: a checklist. 162 pp. Malabar, Florida, Krieger Publishing Company.Google Scholar
Widmer, E.A. & Olsen, O.W. (1967) The life history of Oochoristica osheroffi Meggitt, 1934 (Cyclophyllidea: Anoplocephalidae). Journal of Parasitology 53, 343349.CrossRefGoogle ScholarPubMed
Zamprogno, C. & Teixeira, R.L. (1998) Food habits of the tropical house gecko Hemidactylus mabouia (Reptilia, Gekkonidae) from a sandy coastal Plain of Espirito Santo, eastern Brazil. Revista Brasileira de Biologia 58, 143150.Google Scholar