Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-09T23:01:25.776Z Has data issue: false hasContentIssue false

Schistosoma mansoni: development of primary infections in mice genetically deficient or intact in the fifth component of complement

Published online by Cambridge University Press:  06 April 2009

A. Ruppel
Affiliation:
Institut für Immunologie und Serologic der Universität Heidelberg, Im Neuenheimer Feld 305, D-6900 Heidelberg, F.R.G.
U. Rother
Affiliation:
Institut für Immunologie und Serologic der Universität Heidelberg, Im Neuenheimer Feld 305, D-6900 Heidelberg, F.R.G.
H. J. Diesfeld
Affiliation:
Institut für Tropenhygiene der Universität Heidelberg, Im Neuenheimer Feld 324, D-6900 Heidelberg, F.R.G.

Summary

The influence of the late components of complement (C) on percutaneous primary infections with Schistosoma mansoni was studied in inbred mice genetically deficient or intact in C5. Worm recoveries were diminished in C5-deficient male mice as compared to C5-intact animals. Twenty-four-day-old parasites were also shorter following growth in C5-deficient animals. At 7 weeks after infection, female schistosomes, but not male parasites, were shorter and fewer eggs/schistosome pair were deposited in the livers of C5-deficient as compared to C5-intact male mice. In addition to the presence of C5, the mouse sex was found to influence the outcome of an infection. Schistosomes showed a reduced infection rate and were relatively stunted after 24 days of growth in female mice of the two strains as compared to male mice of the corresponding strains. The results suggest that C5 plays no role in defence against a primary infection in mice.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1982

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

Anwar, A. R. E., McKean, J. R., Smithers, S. R. & Kay, A. B. (1980). Human eosinophil-and neutrophil-mediated killing of schistosomula of Schistosoma mansoni in vitro. Journal of Immunology 124, 1122–9.CrossRefGoogle ScholarPubMed
Anwar, A. R. E., Smithers, S. R. & Kay, A. B. (1979). Killing of schistosomula of Schistosoma mansoni coated with antibody and/or complement by human leukocytes in vitro: Requirement for complement in preferential killing by eosinophils. Journal of Immunology 122, 628–37.CrossRefGoogle ScholarPubMed
Bickle, Q., Long, E., James, E., Doenhoff, M. & Festing, M. (1980). Schistosoma mansoni: Influence of the mouse host's sex, age, and strain on resistance to reinfection. Experimental Parasitology 50, 222–32.CrossRefGoogle ScholarPubMed
Blum, K. & Cioli, D. (1981). Schistosoma mansoni: age-dependent susceptibility to immune elimination of schistosomula artificially introduced in preinfected mice. Parasite Immunology 3, 1324.CrossRefGoogle ScholarPubMed
Cheever, A. W. (1968). Conditions affecting the accuracy of potassium hydroxide digestion techniques for counting Schistosoma mansoni eggs in tissues. Bulletin of the World Health Organization 39, 328–31.Google ScholarPubMed
Cochrane, C. G. & Müller-Eberhard, H. J. (1968). The derivation of two distinct anaphy-latoxin activities from the third and fifth components of human complement. Journal of Experimental Medicine 127, 371–86.CrossRefGoogle ScholarPubMed
Dias da Silva, W. & Kazatchkine, M. D. (1980). Schistosoma mansoni: Activation of the alternative pathway of human complement by schistosomula. Experimental Parasitology 50, 278–86.CrossRefGoogle ScholarPubMed
Machado, A. J., Gazzinelli, G., Pelleqrino, J. & Dias da Silva, W. (1975). Schistosoma mansoni: The role of the complement C3-activating system in the cercaricidal action of normal serum. Experimental Parasitology 38, 20–9.CrossRefGoogle ScholarPubMed
Maddison, S. E., Chandler, F. W., McDougal, J. S., Slemenda, S. B. & Kagan, I. G. (1978). Schistosoma mansoni infection in intact and B cell deficient mice: The effect of pretreatment with BCG in these experimental models. American Journal of Tropical Medicine and Hygiene 27, 966–75.CrossRefGoogle Scholar
McLaren, D. J. & Incani, N. (1982). Schistosoma mansoni: Studies of the resistance acquired by developing schistosomula against immune attack in vitro. Experimental Parasitology (in the Press).CrossRefGoogle Scholar
Ottesen, E. A., Stanley, A. M., Gelfand, J. A., Gadek, J. E., Frank, M. M.Nash, T. E. & Cheever, A. W. (1977). Immunoglobulin and complement receptors on human eosinophils and their role in cellular adherence to schistosomules. American Journal of Tropical Medicine and Hygiene 26, 134–40.CrossRefGoogle ScholarPubMed
Ouaissi, M. A., Santoro, F. & Capron, A. (1980). Schistosoma mansoni: Ultrastructural damages due to complement on schistosomula in vitro. Experimental Parasitology 50, 7482.CrossRefGoogle ScholarPubMed
Pugh, R. N. H., Bell, D. R. & Gilles, H. M. (1980). Malumfashi endemic diseases research project, XV. The potential medical importance of bilharzia in northern Nigeria: a suggested rapid, cheap and effective solution of control of Schistosoma haematobium infection. Annals of Tropical Medicine and Parasitology 74, 597613.CrossRefGoogle ScholarPubMed
Purnell, R. E. (1966). Host-parasite relationships in schistosomiasis. II. The effects of age and sex on the infection of mice and hamsters with cercariae of Schistosoma mansoni and of hamsters with cercariae of Schistosoma haematobium. Annals of Tropical Medicine and Parasitology 60, 5499.Google ScholarPubMed
Ramalho-Pinto, F. J., McLaren, D. J. & Smithers, S. R. (1978). Complement-mediated killing of schistosomula of Schistosoma mansoni by rat eosinophils in vitro. Journal of Experimental Medicine 147, 147–56.CrossRefGoogle ScholarPubMed
Rapp, H. J. & Borsos, T. (1970). Molecular Basis of Complement Action. New York: Meredith Corporation.Google Scholar
Ruppel, A. & Vongerichten, H. (1981). Schistosoma mansoni: Development of primary and secondary infections in inbred mice deficient in the fifth component of complement (C5). Tropenmedizin und Parasitologic 32, 208.Google Scholar
Santoro, F., Lachmann, P. J., Capron, A. & Capron, M. (1979). Activation of complement by Schistosoma mansoni schistosomula: Killing of parasites by the alternative pathway and requirement of IgG for classicial pathway activation. Journal of Immunology 123, 1551–7.CrossRefGoogle Scholar
Sher, A. (1976). Complement-dependent adherence of mast cells to schistosomula. Nature, London 263, 334–6.CrossRefGoogle ScholarPubMed
Sher, A.Knopf, P. M., Gibbons, N., Doughty, B. L. & Von Lichtenberg, F. (1975). Mechanisms of acquired immunity to S. mansoni in the laboratory mouse. Proceedings of the lOth US/Japan Joint Conference on Parasitic Diseases, 132–3.Google Scholar
Smithers, S. R. & Gammage, K. (1980). Recovery of Schistosoma mansoni from the skin, lungs and hepatic portal system of naive mice and mice previously exposed to S. mansoni: evidence for two phases of parasite attrition in immune mice. Parasitology 80, 289300.CrossRefGoogle Scholar
Smithers, S. R. & Miller, K. L. (1980). Protective immunity in murine schistosomiasis mansoni: evidence for two distinct mechanisms. American Journal of Tropical Medicine and Hygiene 29, 832–41.CrossRefGoogle ScholarPubMed
Smithers, S. R. & Terry, R.J. (1965). The infection of laboratory hosts with cercariae of Schistosoma mansoni and the recovery of adult worms. Parasitology 55, 695700.CrossRefGoogle ScholarPubMed
Stek, M., Minard, P., Dean, D. A. & Hall, J. E. (1981). Immunization of baboons with Schistosoma mansoni cercariae attenuated by gamma irradiation. Science 212, 1518–20.CrossRefGoogle Scholar
Tavares, C. A. P., Gazzinelli, G., Mota-Santos, T. A. & Dias Da Silva, W. (1978). Schistosoma mansoni: Complement-mediated cytotoxic activity in vitro and effect of decomplementation on acquired immunity in mice. Experimental Parasitology 46, 145–51.CrossRefGoogle ScholarPubMed
Waksman, B. H. & Cook, J. A. (1975). Report of a conference on newer immunological approaches to schistosomiasis. American Journal of Tropical Medicine and Hygiene 24, 1037–9.CrossRefGoogle ScholarPubMed