Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-10T07:16:15.071Z Has data issue: false hasContentIssue false

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

Published online by Cambridge University Press:  06 April 2009

S. R. Smithers
Affiliation:
Division of Parasitology, National Institute for Medical Research, Mill Hill, London NW7 1AA
K. Gammage
Affiliation:
Division of Parasitology, National Institute for Medical Research, Mill Hill, London NW7 1AA

Summary

New or improved techniques for recovering Schistosoma mansoni from the skin, lungs and liver have enabled us to trace the attrition of a challenge infection in naive (i.e. previously uninfected) and chronically infected mice. Within each experiment, the numbers of schistosomes recovered from the skin of naive mice on day 2 after challenge or from the skin and lungs on days 3, 4 or 5, did not differ significantly from the numbers recovered from the liver on days 14, 21, 28 or 35. Approximately 65% of cercariae which penetrated the skin failed to be recovered from naive mice by any of the assays and it appeared that these schistosomes had already died in the skin in the first 24 h. No further significant loss of the infection was detected in naive mice. In chronically infected mice a further attrition of the challenge infection was demonstrated in two distinct phases. An ‘early phase’ occurred within the first 3 days of exposure and accounted for the death of 30% of the remaining parasites. A ‘late phase’ occurred between days 6 and 14 and accounted for an additional 43% of deaths. Thus, the two phases of attrition accounted for a loss of approximately 73% of the infection that would have survived in naive mice. The late phase of attrition could be demonstrated before the primary infection had matured, in contrast to the early phase of attrition which was seen only after egg laying had commenced. We believe that the early phase of attrition takes place in the skin and the late phase occurs after the schistosomes have left the lungs, either en route for the liver or as soon as they arrive in that organ. The results suggest that there are two distinct mechanisms of immunity against re-infection with S. mansoni in mice.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1980

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., 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
Butterworth, A. E. (1977). Effector mechanisms against schistosomes in vitro. American Journal of Tropical Medicine and Hygiene 26, 2935.CrossRefGoogle ScholarPubMed
Clegg, J. A. & Smithers, S. R. (1968). Death of schistosome cercariae during penetration of the skin. II. Penetration of mammalian skin by Schistosoma mansoni. Parasitology 58, 111–28.CrossRefGoogle ScholarPubMed
Dean, D. A., Minard, P., Murrell, K. D. & Vannier, W. E. (1978). Resistance of mice to secondary infection with Schistosoma mansoni. II. Evidence for a correlation between egg deposition and worm elimination. American Journal of Tropical Medicine and Hygiene 27, 957–65.CrossRefGoogle Scholar
Doenhoff, M., Bickle, Q., Long, E., Baust, J. & McGregor, A. (1978). Factors affecting the acquisition of resistance against Schistosoma mansoni in the mouse. I. Demonstration of resistance to reinfection using a model system that involves perfusion of mice within three weeks of challenge. Journal of Helminthology 52, 173–86.CrossRefGoogle Scholar
Kay, A. B. (1979). The role of the eosinophil. Journal of Allergy and Clinical Immunology 64, 90104.CrossRefGoogle ScholarPubMed
Lewis, F. A. & Colley, D. G. (1977). Modification ofthe lung recovery assay for schistosomula and correlation with worm burdens in mice infected with Schistosoma mansoni. Journal of Parasitology 63, 413–17.CrossRefGoogle Scholar
Lichtenberg, F., Von Sher, A., Gibbons, N. & Doughty, B. L. (1976). Eosinophil-enriched inflammatory response to schistosomula in the skin of mice immune to Schistosoma mansoni. American Journal of Parasitology 84, 479500.Google ScholarPubMed
Miller, P. & Wilson, R. A. (1980). Migration of the schistosomula of Schistosoma mansoni from the lungs to the hepatic portal system. Parasitology (in the Press).CrossRefGoogle Scholar
Phillips, S. M., Reid, W. A. & Sadun, E. H. (1977). The cellular and humoral immune response to Schistosoma mansoni infections in inbred rats. II. Mechanisms during reexposure. Cellular Immunology 28, 7589.CrossRefGoogle 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
Sher, A. (1977). Immunity against Schistosoma mansoni in the mouse. American Journal of Tropical Medicine and Hygiene 26, 20–8.CrossRefGoogle ScholarPubMed
Sher, F. A., Mackenzie, P. & Smithers, S. R. (1974). Decreased recovery of invading parasites from the lungs as a parameter of acquired immunity to schistosomiasis in the laboratory mouse. Journal of Infectious Diseases 130, 626–33.CrossRefGoogle Scholar
Smithers, S. R., McLaren, D. J. & Ramalho-Pinto, F. J. (1977). Immunity to schistosomes: the target. American Journal of Tropical Medicine and Hygiene 26, 1119.CrossRefGoogle ScholarPubMed
Smithers, S. R. & Terry, R. J. (1965). The infection of laboratory hosts with cercariae of Schistosoma mansoni and the recovery ofthe adult worms. Parasitology 55, 695700.CrossRefGoogle Scholar
Smithers, S. R. & Terry, R. J. (1969). Immunity in schistosomiasis. Annals of the New York Academy of Science 160, 826–40.CrossRefGoogle ScholarPubMed