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Role of the lymnaeid snail Pseudosuccinea columella in the transmission of the liver fluke Fasciola hepatica in Egypt

Published online by Cambridge University Press:  27 May 2014

Y. Dar*
Affiliation:
Department of Zoology, Faculty of Science, University of Tanta, Tanta, Egypt INSERM 1094, Faculties of Medicine and Pharmacy, 2, rue du Docteur Raymond Marcland, 87025Limoges Cedex, France
P. Vignoles
Affiliation:
INSERM 1094, Faculties of Medicine and Pharmacy, 2, rue du Docteur Raymond Marcland, 87025Limoges Cedex, France
D. Rondelaud
Affiliation:
INSERM 1094, Faculties of Medicine and Pharmacy, 2, rue du Docteur Raymond Marcland, 87025Limoges Cedex, France
G. Dreyfuss
Affiliation:
INSERM 1094, Faculties of Medicine and Pharmacy, 2, rue du Docteur Raymond Marcland, 87025Limoges Cedex, France
*
*Fax: +2 040 3350804 E-mail: yasser.dar@science.tanta.edu.eg

Abstract

Experimental infections of three Egyptian Pseudosuccinea columella populations with sympatric miracidia of Fasciola sp., coming from cattle- or sheep-collected eggs, were carried out to determine the capacity of this lymnaeid to support larval development of the parasite. Using microsatellite markers, the isolates of Egyptian miracidia were identified as Fasciola hepatica. Apart from being independent of snail origin, prevalences ranging from 60.4 to 75.5% in snails infected with five miracidia of F. hepatica were significantly higher than values of 30.4 to 42.2% in snails with bi-miracidial infections. The number of metacercariae ranged from 243 to 472 per cercarial-shedding snail and was independent of snail origin, parasite origin and miracidial dose used for infection. If P. columella was subjected to two successive bi-miracidial infections with F. hepatica, prevalence of infection was 63.3%, with a mean of 311 metacercariae per snail. These values were clearly greater than those already reported for Radix natalensis infected with the same parasite and the same protocol. Successful experimental infection of P. columella with F. hepatica suggests that this lymnaeid snail is an important intermediate host for the transmission of fascioliasis in Egypt.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2014 

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References

Ahmed, A.H. & Ramzy, R.M. (1999) Infection of two lymnaeid snails with Fasciola gigantica in Giza: A field study. Journal of the Egyptian Society of Parasitology 29, 687696.Google Scholar
Amer, S., Dar, Y., Ichikawa, M., Fukuda, Y., Tada, C., Itagaki, T. & Nakai, Y. (2011) Identification of Fasciola species isolated from Egypt based on sequence analysis of genomic (ITS1 and ITS2) and mitochondrial (NDI and COI) gene markers. Parasitology International 60, 512.CrossRefGoogle ScholarPubMed
Bargues, M.D., González, L.C., Artigas, P. & Mas-Coma, S. (2011) A new baseline for fascioliasis in Venezuela: lymnaeid vectors ascertained by DNA sequencing and analysis of their relationships with human and animal infection. Parasites and Vectors 4, 200218.CrossRefGoogle ScholarPubMed
Boray, J.C. (1978) The potential impact of exotic Lymnaea spp. on fascioliasis in Australasia. Veterinary Parasitology 4, 127141.CrossRefGoogle Scholar
Boray, J.C., Fraser, G.C., Williams, J.D. & Wilson, J.M. (1985) The occurrence of the snail Lymnaea columella on grazing areas in New South Wales and studies on its susceptibility to Fasciola hepatica. Australian Veterinary Journal 62, 46.CrossRefGoogle ScholarPubMed
Brown, D.S. (1994) Freshwater snails of Africa and their medical importance. London, Taylor and Francis.CrossRefGoogle Scholar
Coelho, L.H., Guimarães, M.P. & Lima, W.S. (2008) Influence of shell size of Lymnaea columella on infectivity and development of Fasciola hepatica. Journal of Helminthology 82, 7780.CrossRefGoogle ScholarPubMed
Cruz-Reyes, A. & Malek, E.A. (1987) Suitability of six lymnaeid snails for infection with Fasciola hepatica. Veterinary Parasitology 24, 203210.CrossRefGoogle ScholarPubMed
Dar, Y., Vignoles, P., Rondelaud, D. & Dreyfuss, G. (2003) Fasciola hepatica and F. gigantica: comparative morphometric studies on the redial stage of both species. Parasitology Research 91, 369373.Google Scholar
Dar, Y., Djuikwo Teukeng, F.F., Vignoles, P., Dreyfuss, G. & Rondelaud, D. (2010) Radix natalensis, a potential intermediate host of Fasciola hepatica in Egypt. Parasite 17, 251256.CrossRefGoogle ScholarPubMed
Dar, Y., Amer, S., Courtioux, B. & Dreyfuss, G. (2011) Microsatellite analysis of Fasciola spp. in Egypt. Parasitology Research 109, 17411744.CrossRefGoogle ScholarPubMed
Dar, Y., Amer, S., Mercier, A., Courtioux, B. & Dreyfuss, G. (2012) Molecular identification of Fasciola spp. (Digenea: Fasciolidae) in Egypt. Parasite 19, 177182.CrossRefGoogle ScholarPubMed
Dar, Y., Lounnas, M., Djuikwo Teukeng, F.F., Mouzet, R., Courtioux, B., Hurtrez-Boussès, S., Vignoles, P., Dreyfuss, G. & Rondelaud, D. (2013) Variations in local adaptation of allopatric Fasciola hepatica to French Galba truncatula in relation to parasite origin. Parasitology Research 112, 22552259.CrossRefGoogle ScholarPubMed
Dreyfuss, G., Vignoles, P., Rondelaud, D. & Vareille-Morel, C. (1999) Fasciola hepatica: characteristics of infection in Lymnaea truncatula in relation to the number of miracidia at exposure. Experimental Parasitology 92, 1923.CrossRefGoogle Scholar
El-Shazly, A.M., Helmy, M.M., Haridy, F.M., El-Sharkawy, E.M. & Morsy, T.A. (2002) Fasciola immature stages sought in Lymnaea species and Biomphalaria species in the water bodies of Dakahlia Governorate. Journal of the Egyptian Society of Parasitology 32, 109118.Google ScholarPubMed
Gemmell, N.J., Allen, P.J., Goodman, S.J. & Reed, J.Z. (1997) Interspecific microsatellite markers for the study of pinniped populations. Molecular Ecology 6, 661666.CrossRefGoogle Scholar
Gutiérrez, A., Pointier, J.P., Fraga, J., Jobet, E., Modat, S., Pérez, R.T., Yong, M., Sánchez, J., Loker, E.S. & Théron, A. (2003) Fasciola hepatica: identification of molecular markers for resistant and susceptible Pseudosuccinea columella snail hosts. Experimental Parasitology 105, 211218.CrossRefGoogle ScholarPubMed
Gutiérrez, A., Hernandez, D.F. & Sánchez, J. (2005) Variation of snail's abundance in two water bodies harbouring strains of Pseudosuccinea columella resistant and susceptible to Fasciola hepatica miracidial infection, in Pinar del Río Province, Cuba. Mémorias do Instituto Oswaldo Cruz 100, 725727.CrossRefGoogle Scholar
Gutiérrez, A., Vázquez, A.A., Hevia, Y., Sánchez, J., Correa, A.C., Hurtrez-Boussès, S., Pointier, J.P. & Théron, A. (2011) First report of larval stages of Fasciola hepatica in a wild population of Pseudosuccinea columella from Cuba and the Caribbean. Journal of Helminthology 85, 109111.CrossRefGoogle Scholar
Hubendick, B. (1951) Recent Lymnaeidae. Their variation, morphology, taxonomy, nomenclature, and distribution. Kungliga Svenska Vetenskapsakademiens Handlingar 3, 1223.Google Scholar
Hurtrez-Boussès, S., Durand, P., Jabbour-Zahab, R., Guegan, J.F., Meunier, C., Bargues, M.D., Mas-Coma, S. & Renaud, F. (2004) Isolation and characterization of microsatellite markers in the liver fluke (Fasciola hepatica). Molecular Ecology Notes 4, 689690.CrossRefGoogle Scholar
Lofty, W.M., El-Morshedy, H.N., Abou El-Hoda, M., El-Tawila, M.M., Omar, E.A. & Farag, H.F. (2002) Identification of the Egyptian species of Fasciola. Veterinary Parasitology 103, 323332.Google Scholar
Mas-Coma, S., Bargues, M.D. & Valero, M.A. (2005) Fascioliasis and other plant-borne trematode zoonoses. International Journal for Parasitology 35, 12551278.CrossRefGoogle ScholarPubMed
McKown, R.D. & Ridley, R.K. (1995) Distribution of fasciolosis in Kansas, with results of experimental snail susceptibility studies. Veterinary Parasitology 56, 281291.CrossRefGoogle ScholarPubMed
Ollerenshaw, C.B. (1971) Some observations on the epidemiology of fascioliasis in relation to the timing of molluscicide application in the control of the disease. The Veterinary Record 88, 152164.CrossRefGoogle Scholar
Pointier, J.P., Coustau, C., Rondelaud, D. & Théron, A. (2007) Pseudosuccinea columella (Say 1817) (Gastropoda, Lymnaeidae), snail vector of Fasciola hepatica: first record for France in the wild. Parasitology Research 101, 13891392.CrossRefGoogle Scholar
Ponder, W.F. (1975) The occurrence of Lymnaea (Pseudosuccinea) columella, an intermediate host of Fasciola hepatica, in Australia. Australian Veterinary Journal 51, 494495.CrossRefGoogle ScholarPubMed
Rondelaud, D. & Dreyfuss, G. (1995) Fasciola hepatica: the influence of the definitive host on the characteristics of infection in the snail Lymnaea truncatula. Parasite 2, 275280.CrossRefGoogle Scholar
Salazar, L., Estrada, V.E. & Velásquez, L.E. (2006) Effect of the exposure to Fasciola hepatica (Trematoda: Digenea) on life history traits of Lymnaea cousini and Lymnaea columella (Gastropoda: Lymnaeidae). Experimental Parasitology 114, 7783.CrossRefGoogle ScholarPubMed
Taraschewski, H. (2006) Hosts and parasites as aliens. Journal of Helminthology 80, 99128.CrossRefGoogle ScholarPubMed
Vázquez, A.A., Sánchez, J., Pointier, J.P., Théron, A. & Hurtrez-Boussès, S. (2013) Fasciola hepatica in Cuba: compatibility of different isolates with two intermediate snail hosts, Galba cubensis and Pseudosuccinea columella. Journal of Helminthology, Epub ahead of print.Google ScholarPubMed