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Some effects of cortisone and sex on the biology of coenuriasis in laboratory mice and jackrabbits

Published online by Cambridge University Press:  06 April 2009

Gerald W. Esch
Gerald W. Esch
Affiliation:
Department of Biology, Wake Forest College, Winston-Salem, North Carolina
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Extract

Experimentally infected female mice and naturally infected female jackrabbits are more susceptible to infection with Taenia multiceps than males. It appears that cortisone has the greatest effect in altering rates in mice when injected between days 1 and 14 following exposure of mice. Cortisone elevates infection rates in male mice but not in females. Cortisone does, however, alter the distribution pattern in a similar manner in both sexes. The biology of coenuriasis in rabbits and mice is discussed and compared.

I wish to thank Dr J. R. Egerton of the Merck Institute, Rahway, New Jersey, for supplying cortisone used in this study. I also thank Dr Robert Sullivan and Dr Ralph Amen for their criticisms and suggestions in the preparation of this manuscript.

Type
Research Article
Information
Parasitology , Volume 57 , Issue 1 , February 1967 , pp. 175 - 179
Copyright
Copyright © Cambridge University Press 1967

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References

REFERENCES

Besch, E. D. (1964). Biology of Cooperia punctata (Nematodea: Trichostrongylidae) in the domestic rabbit. J. Parasit. 51, 139–44.CrossRefGoogle Scholar
Brumpt, E. (1936). Précis de Parasitologie, 5th ed.Paris: Masson.Google Scholar
Campbell, D. H. & Melcher, L. R. (1940). Relationship of sex factors to resistance against Cysticercus crassicollis in rats. J. infect. Dis. 66, 184–8.Google Scholar
Curtis, M. R., Dunning, W. F. & Bullock, F. D. (1933). Genetic factors in relation to the etiology of malignant tumours. Am. J. Cancer 17, 894–923.CrossRefGoogle Scholar
Esch, G. W. (1964). The effects of cortisone and pre-infection starvation in the establishment of larval Multiceps serialis in mice. J. Elisha Mitchell scient. Soc. 80, 114–20.Google Scholar
Esch, G. W. & Self, J. T. (1965). A critical study of the taxonomy of Taenia pisiformis Bloch, 1780; Multiceps multiceps (Leske, 1780); and Hydatigera taeniaeformis Batsch, 1786. J. Parasit. 51, 932–7.Google Scholar
Larsh, J. E., Race, G. J., Goulson, H. T. & Weatherly, N. F. (1966). Studies on delayed (cellular) hyper-sensitivity in mice infected with Trichinella spiralis. III. Serologic and histopathologic findings in recipients given peritoneal exudate cells. J. Parasit. 52, 146–56.Google Scholar
Mathies, A. H. (1959). Certain aspects of the host–parasite relationship of Aspicularis tetraptera, a mouse pinworm. II. Sex resistance. Expl Parasit. 8, 39–45.Google Scholar
Olivier, L. (1962). Studies on natural resistance to Taenia taeniaeformis in mice. II. The effect of cortisone. J. Parasit. 48, 758–62.Google Scholar
Olsen, O. W., 1962. Animal Parasites, Their Biology and Life Cycles. Minneapolis, Minn.: Burgess Publishing Co.Google Scholar
Voge, M. & Berntzen, A. K. (1963). Asexual multiplication of larval tapeworms as the cause of fatal parasitic ascites in dogs. J. Parasit. 49, 983–8.CrossRefGoogle ScholarPubMed