Hostname: page-component-848d4c4894-2pzkn Total loading time: 0 Render date: 2024-05-10T06:29:48.168Z Has data issue: false hasContentIssue false

Metacercarial aggregation in Digenea (Fasciola hepatica and Paramphistomum daubneyi): environmental or species determinism?

Published online by Cambridge University Press:  12 April 2024

M. Abrous
Affiliation:
Laboratoire d'Histopathologie Parasitaire, Faculté de Médecine Faculté de Pharmacie, 2, rue du Docteur Raymond Marcland, 87025 Limoges Cedex, France Laboratoire de Parasitologie, Faculté de Pharmacie, 2, rue du Docteur Raymond Marcland, 87025 Limoges Cedex, France
C. Vareille-Morel
Affiliation:
Laboratoire de Malacologie Appliquée, Faculté des Sciences, 123, avenue Albert Thomas, 87060 Limoges Cedex, France
D. Rondelaud*
Affiliation:
Laboratoire d'Histopathologie Parasitaire, Faculté de Médecine Faculté de Pharmacie, 2, rue du Docteur Raymond Marcland, 87025 Limoges Cedex, France
G. Dreyfuss
Affiliation:
Laboratoire de Parasitologie, Faculté de Pharmacie, 2, rue du Docteur Raymond Marcland, 87025 Limoges Cedex, France
J. Cabaret
Affiliation:
Laboratoire de Malacologie Appliquée, Faculté des Sciences, 123, avenue Albert Thomas, 87060 Limoges Cedex, France
*
*Author for correspondence Fax: 33 5 55 43 58 93 E-mail: rondelaud@pharma.unilim.fr

Abstract

Metacercarial aggregation of Fasciola hepatica and Paramphistomum daubneyi was studied under experimental conditions to determine if the formation of these aggregates was influenced by environmental factors, or it was a characteristic of trematode species. This process was studied using the confinement of infected snails on the bottom of Petri dishes (diameter, 14 cm) for 3 days. The formation of metacercarial aggregates of F. hepatica was not significantly modified by environmental factors such as intensity and duration of lighting, quality and volume of water. Metacercariae of F. hepatica were more numerous on the Petri dish walls and 63.9% of them constituted aggregates. In contrast, most metacercariae of P. daubneyi were found on the Petri dish bottoms and 78.3% of them were isolated or in groups of two metacercariae each. The mean number of metacercariae per aggregate ranged from 6.7 to 12.2 in the case of F. hepatica, and from 2.7 to 4.5 in the case of P. daubneyi. However, these mean numbers were independent of the site of cercarial attachment. The tendency of cercariae to form metacercarial aggregations was a characteristic of F. hepatica and was species determined.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2001

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

references

Abrous, M., Rondelaud, D., Dreyfuss, G. & Cabaret, J. 1999a Infection of Lymnaea truncatula and Lymnaea glabra by Fasciola hepatica and Paramphistomum daubneyi in farms of central France. Veterinary Research 30, 113118.Google ScholarPubMed
Abrous, M., Rondelaud, D. & Dreyfuss, G. 1999b Influence of low temperatures on the cercarial shedding of Paramphistomum daubneyi from the snail Lymnaea truncatula . Parasite 6, 8588.10.1051/parasite/1999061085CrossRefGoogle ScholarPubMed
Anderson, R.M. (1978) Population dynamics of snail infection by miracidia. Parasitology 77, 201224.10.1017/S0031182000049398CrossRefGoogle ScholarPubMed
Anderson, R.M. & Gordon, D.M. (1982) Processes influencing the distribution of parasite numbers within host populations with special emphasis on parasite-induced host mortalities. Parasitology 85, 373398.10.1017/S0031182000055347CrossRefGoogle ScholarPubMed
Anderson, R.M. & May, R.M. (1985) Helminth infections of humans: mathematical models, population dynamics, and control. Advances in Parasitology 24, 1101.10.1016/S0065-308X(08)60561-8CrossRefGoogle ScholarPubMed
Dreyfuss, G. & Rondelaud, D. (1994) Fasciola hepatica: a study on the shedding of cercariae from Lymnaea truncatula raised under constant conditions of temperature and photoperiod. Parasite 1, 401404.10.1051/parasite/1994014401CrossRefGoogle Scholar
May, R.M. (1977) Dynamical aspects of host-parasite associations: Crofton's model revisited. Parasitology 75, 259276.10.1017/S0031182000051805CrossRefGoogle Scholar
Pecheur, M. (1967) La cercaire de Fasciola hepatica. Le rôle de la couleur, de la lumière et des plantes sur le choix de l'endroit de fixation. La cercaire est-elle infestante?. Annales de Médecine Vétérinaire 6, 349355.Google Scholar
Pecheur, M. (1971) A few considerations on the cercariae and metacercariae of Fasciola hepatica. Proceedings, Second International Liverfluke Colloquium, Wageningen, 1967 148149.Google Scholar
Roberts, E.W. (1950) Studies on the life-cycle of Fasciola hepatica (Linnaeus) and of its snail host, Limnaea (Galba) truncatula Müller in the field and under controlled conditions. Annals of Tropical Medicine and Parasitology 44, 187206.10.1080/00034983.1950.11685441CrossRefGoogle Scholar
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, 275280.10.1051/parasite/1995023275CrossRefGoogle Scholar
Rondelaud, D. & Dreyfuss, G. (1997) Variability of Fasciola infection in Lymnaea truncatula as a function of snail generation and snail activity. Journal of Helminthology 71, 161166.10.1017/S0022149X00015844CrossRefGoogle Scholar
Taylor, E.L. (1965) Fascioliasis and the liver-fluke. 235 pp. FAO Agricultural Studies, no. 64. Google Scholar