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Dynamics of gastropod infection by first-stage larvae of protostrongylid nematodes — a model

Published online by Cambridge University Press:  06 April 2009

P. Řezáč
Affiliation:
Institute of Parasitology, Czechoslovak Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czechoslovakia
P. Kindlmann
Affiliation:
and Laboratory of Biomathematics, Czechoslovak Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czechoslovakia
I. Dostálková
Affiliation:
and Laboratory of Biomathematics, Czechoslovak Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czechoslovakia
E. Holasová
Affiliation:
Institute of Parasitology, Czechoslovak Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czechoslovakia

Summary

For the description of the dynamics of snail infection by the 1st-stage larvae of protostrongylid nematodes, Skorping (1988) used the miracidia-snail model (Anderson, 1978). Here it is shown that, in contrast to miracidia, in protostrongylids the instantaneous rate of infection, α, is strongly dependent on the experimental design (factors like host size and size of the experimental arena). With respect to this, Anderson's model is modified by incorporation of the experimental design. The parameter α in its new sense as the rate of penetration (probability that the infective larva will penetrate into the host during a time unit) is shown to remain dependent, although much less so, on the experimental design. Only the inclusion of the assumed effect of mucus, which decreases the rate of penetration, yields a parameter α0 (the initial rate of penetration), which is completely independent of the design of the experiment, is species-specific, and also gives the best fit to the empirical data. As the above-mentioned factors can strongly influence the value of the instantaneous rate of infection in the laboratory experiments, α0 is more suitable as a measure of either the larval infectivity for the snail or snail susceptibility to infection by the protostrongylid larvae.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1993

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References

REFERENCES

Anderson, R. M. (1978). Population dynamics of snail infection by miracidia. Parasitology 77, 201–24.CrossRefGoogle ScholarPubMed
Anderson, R. M. (1982). Epidemiology of infectious disease agents. In Modern Parasitology (ed. Cox, F. E. G.), pp. 204251. Oxford: Blackwell Scientific Publications.Google Scholar
Cabaret, J. (1987a). Regulation of infection by a nematode (Muellerius capillaris) in the snail Theba pisana. Journal of Invertebrate Pathology 49, 242–5.CrossRefGoogle ScholarPubMed
Cabaret, J. (1987b). Age susceptibility of molluscan intermediate hosts to protostrongylid nematodes. Journal of Parasitology 73, 857–8.CrossRefGoogle ScholarPubMed
Gerichter, Ch. B. (1948). Observations on the life history of lung nematodes using snails as intermediate hosts. American Journal of Veterinary Research 9, 109–12.Google Scholar
Godan, D. (1983). Pest Slugs and Snails: Biology and Control. Berlin: Springer-Verlag.CrossRefGoogle Scholar
Joyeux, C. & Gaud, J. (1946). Recherches helminthologiques Marocaines (suite). Etudes sur la pneumonie vermineuse. Archives de l'institut Pasteur Maroc 3, 383461.Google Scholar
Kassai, T. (1958). Larvae of protostrongylins in snails. Acta veterinaria Academiae Scientiarum hungaricae 8, 223–36.Google Scholar
Lankester, M. & Anderson, R. C. (1968). Gastropods as intermediate hosts of Pneumostrongylus tenuis Dougherty of white-tailed deer. Canadian Journal of Zoology 46, 373–83.CrossRefGoogle Scholar
Morrondo-Pelayo, M. P. & Manga-Gonzalez, M. Y. (1982). Experimental study on the susceptibility of five Helicidae species to larvae of protostrongylinae. Malacologia 22, 23–8.Google Scholar
Platt, T. R. & Samuel, W. M. (1984). Mode of entry of Parelaphostrongylus odocoilei. (Nematoda: Metastrongyloidea) into four species of terrestrial gastropods. Proceedings of the Helminthological Society of Washington 51, 205–7.Google Scholar
Rose, J. H. (1957). Observations on the larval stages of Muellerius capillaris within the intermediate hosts Agriolimax agrestis. Journal of Helminthology 31, 116.CrossRefGoogle ScholarPubMed
Schittkowski, K. (1985). NLPQLD: A FORTRAN subroutine solving constrained nonlinear programming problems. Annals of Operations Research 5, 485500.CrossRefGoogle Scholar
Skorping, A. (1982). Elaphostrongylus rangiferi: Influence of temperature, substrate, and larval age on the infection rate in the intermediate snail host, Arianta arbustorum. Experimental Parasitology 54, 222–8.CrossRefGoogle ScholarPubMed
Skorping, A. (1985). Lymnaea stagnalis as experimental intermediate host for the protostrongylid nematode Elaphostrongylus rangiferi. Zeitschrift für Parasitenkunde 71, 265–70.CrossRefGoogle Scholar
Skorping, A. (1988). The effect of density of first-stage larvae of Elaphostrongylus rangiferi on the infection rate in the snail intermediate host. Parasitology 96, 487–92.CrossRefGoogle ScholarPubMed
Skorping, A. & Halvorsen, O. (1980). The susceptibility of terrestrial gastropods to experimental infection with Elaphostrongylus rangiferi Mitskevich (Nematoda: Metastrongyloidea). Zeitschrift für Parasitenkunde 62, 714.CrossRefGoogle Scholar
Yousif, F. & Lämmler, G. (1977). The mode of infection with and the distribution of Angiostrongylus cantonensis larvae in the experimental intermediate host Biomphalaria glabrata. Zeitschrift für Parasitenkunde 53, 247–50.CrossRefGoogle Scholar