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Effect of concurrent infection with Muellerius capillaris on the development of redial generations of Fasciola hepatica in Lymnaea truncatula

Published online by Cambridge University Press:  05 June 2009

P. Hourdin
Affiliation:
Faculté de Médecine, Laboratoire d'Histologie, Unité d'Histopathologie Parasitaire, 2, Rue du Docteur Raymond Marcland, 87025 Limoges cédex, France
D. Rondelaud
Affiliation:
Faculté de Médecine, Laboratoire d'Histologie, Unité d'Histopathologie Parasitaire, 2, Rue du Docteur Raymond Marcland, 87025 Limoges cédex, France
J. Cabaret
Affiliation:
Institut National de la Recherche Agronomique, Station de Pathologie Aviaire et de Parasitologie, Unité d'Ecologie des Parasites, 37380 Nouzilly cédex, France

Abstract

The rediae of Fasciola hepatica were counted according to generation in adult and juvenile Lymnaea truncatula following single infection with Fasciola hepatica, double infection with F. hepatica and then Muellerius capillaris, or double infection with M. capillaris and F. hepatica. The rediae found in double infections were essentially first generation and an early cohort from the second generation. The following differences were observed in adult snails which underwent double infection when compared to corresponding single infections: i) dependent rediae were almost completely absent; ii) degenerating independent rediae were found in identical or decreased numbers; iii) living independent rediae of the first generation were decreased in number, while those of the second generation had variable decreased numbers. The results were similar in juvenile snails with double infections, except that the numbers of degenerating independent rediae were higher than those found in corresponding single infections and the numbers of rediae of the second generation were increased. The order of exposure in double infections had no influence on the number and maturation of fasciolid rediae.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1992

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References

REFERENCES

Cabaret, J. (1980) Molilité et infestivité des larves LI de protostrongylides: facteurs de variation. Annales de Parasitologie Humaine et Comparée, 55, 571581.CrossRefGoogle Scholar
Cabaret, J. (1984) Sheep and goats: epidemiology of protostrongylid lungworm infections. International Goat and Sheep Research, 2, 142152.Google Scholar
Chipev, N., Vassilev, I. & Samnaliev, P. (1985) Interactions between Paramphistomum c.f. daubneyi Dinnik, 1962 and Fasciola hepatica L. in successive cross-invasions of Lymnaea (Galba) truncatula. Helminthologia, 20, 8088.Google Scholar
Christie, J. D. & Prentice, M. A. (1978) The relationship between numbers of Schistosoma mansoni daughter sporocysts and miracidia. Annals of Tropical Medicine and Parasitology, 72, 197198.CrossRefGoogle ScholarPubMed
Combes, C. (1982) Trematodes: antagonism between species and sterilizing effects on snails in biological control. Parasitology, 84, 151175.CrossRefGoogle Scholar
Combes, C. (1983) Usage des trématodes stérilisants-dominants pour le contrôle de certaines maladies parasitaires. Etat des recherches. Symbioses. 15, 93125.Google Scholar
Hata, H., Orido, M., Yokogawa, M. & Kosina, S. (1988) Schistosoma japonicum and Paragoninus ohirai: antagonism between S.japonicum and P. ohirai in Oncomelania nosophora. Experimental Parasitology, 65, 125130.CrossRefGoogle ScholarPubMed
Hourdin, P., Rondelaud, D. & Cabaret, J. (1990) Interactions entre Fasciola hepatica L. et Muellerius capillaris Müller chez le Mollusque Lymnaea truncatula Müller. Bulletin de la Société Française de Parasitologie, 8, 111118.Google Scholar
Lim, H. K. & Heyneman, D. (1972) Intramolluscan intertrematode antgonism: a review of factors influencing the host-parasite system and its possible role in biological control. Advances in Parasitology, 10, 191268.CrossRefGoogle ScholarPubMed
Ollerenshaw, C. B. (1971) Some observations on the epidemiology of fascioliasis in relation to the timing of molluscicide applications in the control of the disease. Veterinary Record, 88, 152164.CrossRefGoogle Scholar
Rondelaud, D. & Barthe, D. (1978) Arguments et propositions pur une nouvelle interprétation de l'évolution de Fasciola hepatica L. dans Lymnaea (Galba) truncatula Müller. Annales de Parasitologie Humaine et Comparée, 53, 201213.CrossRefGoogle Scholar
Rondelaud, D. & Barthe, D. (1982) Les générations rédiennes de Fasciola hepatica L. chez Lynmaea truncatula Müller. A propos des effets de plusieurs facteurs. Annales de Parasitologie Humaine et Comparée, 57, 245262.CrossRefGoogle Scholar
Rondelaud, D. & Barthe, D. (1987) Fasciola hepatica L.: étude de la productivité d'un sporocyste en fonction de la taille de Lymnaea truncatula Müller. Parasitology Research, 74, 155160.CrossRefGoogle Scholar
Smith, G. (1984) The relationship between the size of Lymnaea truncatula naturally infected with Fasciola hepatica and the intensity and maturity of the redial infection. Journal of Helminthology, 58, 123128.CrossRefGoogle ScholarPubMed
Urban, E. (1980) Studies on lung nematodes (Protostrongylidae, Dictyocaulidae) in sheep of the Podhale region, Tatra highlands. II. Intermediate hosts of Protostrongylidae. Acta Parasitologica Polonica, 26, 6374.Google Scholar
Zischke, J. A. (1968) Reproduction of Echinostoma revolutum rediae when transferred to uninfected snails of different sizes. Journal of Parasitology, 54, 3942.CrossRefGoogle ScholarPubMed