Hostname: page-component-76fb5796d-5g6vh Total loading time: 0 Render date: 2024-04-28T23:08:33.207Z Has data issue: false hasContentIssue false

Immunity to intestinal tapeworms: the rejection of Hymenolepis citelli by mice

Published online by Cambridge University Press:  06 April 2009

C. A. Hopkins
Affiliation:
Wellcome Laboratories for Experimental Parasitology, University of Glasgow, Bearsden, Glasgow G61 1QH
H. E. Stallard
Affiliation:
Wellcome Laboratories for Experimental Parasitology, University of Glasgow, Bearsden, Glasgow G61 1QH

Extract

Approximately 90% of Hymenolepis citelli cysticercoids given to 6-week-old male CFLP mice by stomach tube became established. Equally high recovery rates were obtained from administering 1, 3 and 6 cysticercoids.

In 1-worm infections worms increase in weight until about day 25–28 post infection. After a few days at maximum weight (mean weights of worms 24–42 mg) there is a small, 10–25%, decrease in weight, after which there is little change in weight up to day 90 (as long as studied).

One-worm infections survived without loss until day 30, after which a slow loss occurred, but only in two experiments, both with older mice, did loss exceed 50% by day 80. In 3-worm infections worms were rejected between days 17 and 30, but loss varied from 50 to 80% during this period in replicate experiments. With 6-worm infections rejection occurred over a shorter period (days 17–22), was more uniform between experiments and was more complete, over 75% of worms being lost. In both 3- and 6-worm infections a residual population, usually of only a single worm, persisted in 20–50% of the mice until the end of the experiments (day 63–78).

Cortisone prevented loss of worms from both 3- and 6-worm infections; worms continued to grow until day 25 ± 2 (as in 1-worm infections), by which time they were considerably larger than (the surviving) worms in mice not receiving cortisone. The biomass (worm burden per mouse) remained constant from day 25 to 55 in mice receiving cortisone.

The results are discussed with particular reference to: H. diminuta and the evidence that mice do mount an immunological response against tapeworms in the intestine; the existence of an antigenic threshold in mice; the apparent existence of a similar rejection pattern in a natural population of H. citelli in Peromyscus maniculatus, and hence the importance of immunity as a factor preventing gradual increase in number of tapeworms in the intestine during the life of a host.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1974

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

Ford, B. R. (1972). Hymenolepis citelli: Development and chemical composition in hypothermic ground squirrels. Experimental Parasitology 32, 6270.CrossRefGoogle ScholarPubMed
Grundmann, A. W. & Frandsen, J. C. (1960). Definitive host relationships of the helminth parasites of the deer mouse, Peromyscus maniculatus, in the Bonneville Basin of Utah. Journal of Parasitology 46, 673–8.CrossRefGoogle ScholarPubMed
Guss, V. M. & Grundmann, A. W. (1968). A method for experimental per os infection of insectivorous hosts. Journal of Parasitology 54, 88.CrossRefGoogle ScholarPubMed
Hopkins, C. A., Subramanian, G. & Stallard, H. (1972 a). The development of Hymenolepis diminuta in primary and secondary infections in mice. Parasitology 64, 401–12.Google Scholar
Hopkins, C. A., Subramanian, G. & Stallard, H. E. (1972 b). The effect of immuno-suppressants on the development of Hymenolepis diminuta in mice. Parasitology 65, 111–20.CrossRefGoogle Scholar
McLeod, J. A. (1933). A parasitological survey of the genus Citellus in Manitoba. Canadian Journal of Research 9, 108–27.Google Scholar
Moss, G. D. (1972). The effect of cortisone acetate treatment on the growth of Hymenolepis microstoma in mice. Parasitology 64, 311–20.Google Scholar
Ogilvie, B. M. & Jones, V. E. (1971). Nippostrongylus brasiliensis: A review of immunity and the host/parasite relationship in the rat. Experimental Parasitology 29, 138–77.CrossRefGoogle ScholarPubMed
Read, C. P. (1959). The role of carbohydrates in the biology of cestodes. VIII. Some conclusions and hypotheses. Experimental Parasitology 8, 365–82.Google Scholar
Read, C. P. (1967). Longevity of the tapeworm, Hymenolepis diminuta. Journal of Parasitology 53, 1055–6.CrossRefGoogle ScholarPubMed
Voge, M. (1956). Studies on the life history of Hymenolepis citelli (McLeod, 1933) (Cestoda: Cyclophyllidea). Journal of Parasitology 42, 485–9.Google Scholar
Wakelin, D. (1973). The stimulation of immunity to Trichuris muris in mice exposed to low-level infections. Parasitology 66, 181–9.Google Scholar
Wassom, D. L., Guss, V. M. & Grundmann, A. W. (1973). Host resistance in a natural host-parasite system. Resistance to Hymenolepis citelli by Peromyscus maniculatus. Journal of Parasitology 59, 117–21.CrossRefGoogle Scholar
Weinmann, C. F. (1966). Immunity mechanisms in cestode infections. In Biology of Parasites (ed. Soulsby, E. J. L.), pp. 301–20. Philadelphia: Academic Press.Google Scholar