Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-22T09:00:16.354Z Has data issue: false hasContentIssue false

Schistosoma mansoni: evidence that vascular abnormalities correlate with the ‘non- permissive’ trait in 129/Ola mice

Published online by Cambridge University Press:  06 April 2009

A. A. F. Elsaghier
Affiliation:
Division of Parasitology, National Institute for Medical Research, Mill Hill, London NW7 1AA
D. J. Mclaren
Affiliation:
Division of Parasitology, National Institute for Medical Research, Mill Hill, London NW7 1AA

Summary

The pulmonary and portal vasculature of naïve mice of the 129/Ola and CBA/Ca strains has been studied by means of the vasculature casting technique. This involves injection of pigmented vinylite resin into the arterial and venous systems, followed by digestion of the tissues with KOH. The peripheral vessels of the arterial and portal systems of CBA/Ca mice were numerous and highly branched. In contrast, casts prepared from 70–80% of naïve 129/Ola mice showed dramatic reductions in the number and extent of the peripheral vessels. In addition, such vessels appeared severely truncated. The remaining 20–30% of naïve 129/Ola mice yielded lung and liver casts that were indistinguishable from the CBA/Ca casts. Casts prepared from 129/Ola mice infected 6 weeks previously with Schistosoma mansoni cercariae showed the same segregation; faecal smears, together with observations of presence or absence of gross pathology in such mice confirmed that the vascular changes correlated with the ‘non-permissive trait’. We propose that such alterations facilitate the reportedly abnormal migration of schistosomes from the liver to the lungs in ‘non-permissive’ 129/Ola mice.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1989

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

Davern, K. M., Tiu, W. U., Wright, M. D., Garcia, E. G. & Mitchell, G. F. (1987). Responses in mice to Sj26, a glutathione S-transferase of Schistosoma japonicum worms. Immunology and Cell Biology 65, 473–82.CrossRefGoogle ScholarPubMed
Dean, D. A., Bukowski, M. A. & Cheever, A. W. (1981). Relationship between acquired resistance, portal hypertension and lung granulomas in ten strains of mice infected with Schistosoma mansoni. American Journal of Tropical Medicine and Hygiene 30, 806–14.CrossRefGoogle ScholarPubMed
Durand, P., Borrone, C. & Della Cella, G. (1966). A new mucopolysaccharide lipid storage disease ? Lancet 2, 1313.CrossRefGoogle Scholar
Durand, P., Borrone, C. & Della Cella, G. (1969). Fucosidosis. Journal of Pediatrics 75, 665.CrossRefGoogle ScholarPubMed
Durand, P., Borrone, C., Della Cella, G. & Philippart, M. (1968). Fucosidosis. Lancet 1, 1198.CrossRefGoogle Scholar
Elsaghier, A. A. F., Knopf, P. M., Mitchell, G. F. & Mclaren, D. J. (1989). Schistosoma mansoni: evidence that ‘non-permissiveness‘ in 129/Ola mice involves worm relocation and attrition in the lungs. Parasitology 99, 365–75.CrossRefGoogle ScholarPubMed
Fanning, M. M. & Kazura, J. W. (1984). Genetic-linked variation in susceptibility of mice to schistosomiasis mansoni. Parasite Immunology 6, 95103.CrossRefGoogle ScholarPubMed
Garcia, E. G., Tiu, W. U. & Mitchell, G. F. (1983). Innate resistance to Schistosoma japonicum in a proportion of 129/J mice. Journal of Parasitology 69, 613–15.CrossRefGoogle Scholar
Johnson, W. G. & Hong, J. L. (1986). Variation in alpha-L-fucosidase properties among 28 inbred mouse strains: six strains have high enzyme activity and heat-stable enzyme with a variant pH-activity curve; twenty-two strains have low activity and heat-labile enzyme. Biochemical Genetics 24, 469–83.CrossRefGoogle Scholar
Johnson, W. G., Hong, J. L. & Knights, S. M. (1986). Variation in ten lysosomal hydrolase enzyme activities in inbred mouse strains. Biochemical Genetics 24, 891909.CrossRefGoogle ScholarPubMed
Joky, A., Cornu, M., Louis, D. & Grimaud, J. A. (1978). Polyvinylchloride (PVC) particle implantation in mouse liver. A technique for experimental study of schistosome egg-induced liver pathology. Experientia 34, 547–9.CrossRefGoogle Scholar
Mitchell, G. F. (1989). Glutathione S-transferases: potential components of anti-schistosome vaccines. Parasitology Today 5, 34–7.CrossRefGoogle ScholarPubMed
Rogers, M. V. (1986). Schistosoma mansoni: studies of antigen recognition and immune expression inchronically infected and vaccinated guinea pigs. Ph.D. thesis, Brunei University, Uxbridge, Middlesex, U.K.Google Scholar
Smith, D. B., Davern, K. M., Board, B. G., Tiu, W. U., Garcia, E. G. & Mitchell, G. F. (1986). Mr 26,000 antigen of Schistosoma japonicum recognised by resistant WEHI 129/J mice is a parasite glutathione S-transferase. Proceedings of the National Academy of Sciences, USA 83, 8703–7.CrossRefGoogle Scholar
Smithers, S. R. & Doenhoff, M. J. (1982). Schistosomiasis. In Immunology of Parasitic Infections (ed. Cohen, S. & Warren, K. S.), Oxford: Blackwell Scientific Publications. pp. 527607.Google Scholar
Smithers, S. R., Simpson, A. J. G., Yi, X., Omar-Ali, P., Kelly, C. & Mclaren, D. J. (1987). The mouse model of schistosome immunity. Acta Tropica 44 (Suppl.) 1230.Google Scholar
Smithers, S. R. & Terry, R. J. (1965). Infection of laboratory hosts with cercariae of Schistosoma mansoni and the recovery of adult worms. Parasitology 55, 695700.CrossRefGoogle ScholarPubMed
Taylor, J. B., Vidal, A., Torpier, G., Meyer, D. J., Roitsch, C., Balloul, J., Southan, C., Sondermeyer, P., Pemble, S., Lecocq, J., Capron, A. & Ketterer, B. (1988). The glutathione transferase activity and tissue distribution of a cloned Mr 28 K protective antigen of Schistosoma mansoni. EMBO Journal 7, 465–72.CrossRefGoogle Scholar
Tiu, W. U., Ehl, A., Walker, J. C., Garcia, E. G., Smith, D. B. & Mitchell, G. F. (1986). Resistance of 129/J mice to Schistosoma mansoni infection. Australian Journal of Experimental Biology and Medical Science 64, 345–9.CrossRefGoogle ScholarPubMed
Van Hoof, F. & Hers, H. G. (1968). Mucopolysaccharidosis by absence of α-fucosidase. Lancet 1, 1198.CrossRefGoogle ScholarPubMed
Wilson, R. A. (1987). Cercariae to liver worms: development and migration in the mammalian host. In The Biology of Schistosomes: From Genes to Latrines (ed. Rollinson, D. & Simpson, A. J. G.), London: Academic Press. pp. 115–46.Google Scholar
Wright, M. D., Rogers, M. V., Davern, K. M. & Mitchell., G. F. (1988 a). Schistosoma mansoni antigens differentially recognised by resistant WEHI 129/J mice. Infection and Immunity 56, 2948–52.CrossRefGoogle ScholarPubMed
Wright, M. D., Tiu, W. U., Wood, S. M., Walker, J. C., Garcia, E. G. & Mitchell, G. F. (1988 b) Schistosoma mansoni and Schistosoma japonicum worm numbers in 129/J mice of two types and dominance of susceptibility in Fl hybrids. Journal of Parasitology 74, 618–22.CrossRefGoogle Scholar