Hostname: page-component-8448b6f56d-42gr6 Total loading time: 0 Render date: 2024-04-18T19:25:57.642Z Has data issue: false hasContentIssue false

Sterile immunity, coinfectious immunity and strain differences in Babesia bigemina infections

Published online by Cambridge University Press:  06 April 2009

L. L. Callow
Affiliation:
Queensland Department of Primary Industries, Animal Research Institute, Yeerongpilly, Brisbane, Australia

Extract

The acquired immunity of twenty-eight splenectomized and twenty-three intact cattle following primary inoculation with either of two strains (the Y and the R strain) of Babesia bigemina was investigated. Some of these animals were carriers, while others had ceased to be infected. Observations were made on the response of splenectomized animals challenged up to four times with the original infecting (homologous) strain and finally with the heterologous strain.

In the splenectomized animals, a total of sixty-three homologous challenges produced parasitaemias in only twenty-seven instances, and these were generally delayed and of lower intensity than in control animals. Fifteen negative transmission tests performed shortly after thirty-two challenges showed that it was difficult to re-establish the homologous strain in some animals that had achieved self-cure. Substantial homologous immunity had developed within 16 weeks of the primary infection in animals which were no longer carrying B. bigemina.

All twenty-one splenectomized animals subjected to heterologous challenge developed well-marked parasitaemias. Nine of these had been highly immune to homologous challenge 2 weeks earlier. Eight of the twenty-one were carriers at the time of challenge and these showed much lower parasitaemias than the self-cured animals which almost invariably were acutely affected.

Challenges of twenty-three intact steers confirmed that the two strains differed immunologically. Six of twelve challenged homologously failed to show detectable parasitaemia, whereas all eleven challenged heterologously developed parasitaemias.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1967

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

Box, E. D. & Gingrich, W. D. (1958). Acquired immunity to Plasmodium berghei in the white mouse. J. infect. Dis. 103, 291300.CrossRefGoogle ScholarPubMed
Callow, L. L. (1964). Strain immunity in babesiosis. Nature, Lond. 204, 1213–4.CrossRefGoogle ScholarPubMed
Callow, L. L. & Hoyte, H. M. D. (1961 a). The separation of Babesia bigemina from Babesia argentina and Theileria mutans. Aust. vet. J. 37, 6670.CrossRefGoogle Scholar
Callow, L. L. & Hoyte, H. M. D. (1961 b). Transmission experiments using Babesia bigemina, Theileria mutans, Borrelia sp. and the cattle tick, Boophilus microplus. Aust. vet. J. 37, 381–90.CrossRefGoogle Scholar
Coggeshall, L. T., Rice, F. A. & Yount, E. H. (1948). The cure of recurrent vivax malaria and status of immunity thereafter. 4th Int. Congr. trop. Med., Washington, D.C. 1, 749–55.Google Scholar
Corradetti, A. (1955). Studies on comparative pathology and immunology in Plasmodium infections of mammals and birds. Trans. R. Soc. trop. Med. Hyg. 49, 311–38.Google Scholar
Gingrich, W. D. (1948). Duration of immunity to malaria (Plasmodium cathemerium) in the canary. J. nat. Malar. Soc. 7, 109–17.Google Scholar
Krishnan, K. V., Smith, R. O. A. & Lal, C. (1934). Immunity to malaria in monkeys and the effect of splenectomy on it. Indian J. med. Res. 21, 639–47.Google Scholar
Legg, J. (1935). The occurrence of bovine babesiellosis in Northern Australia. Pamphl. Coun. sci. industr. Res. Aust. no. 56, pp. 48.Google Scholar
Legg, J. (1936). The treatment of piroplasmosis (P. bigeminum) with akiron. Aust. vet. J. 12, 227–30.CrossRefGoogle Scholar
Maier, J. & Coggeshall, L. T. (1944). The duration of immunity to Plasmodium knowlesi malaria in rhesus monkeys. J. exp. Med. 79, 401–30.Google Scholar
Neitz, W. O. (1957). Theileriosis, Gonderiosis and Cytauxzoonoses. A review. Onderstepoort J. vet. Res. 27, 275430.Google Scholar
Sergent, E., Parrot, L. & Donatien, A. (1924). Une question de terminologie: Immuniser et Prémunir. Bull. Soc. Path. exot. 17, 37–8.Google Scholar
Weitz, B. (1964). The reaction of trypanosomes to their environment. 14th Symp. Soc. gen. Microbiol., Lond. p. 112–21.Google Scholar
Wolfson, F. & Winter, M. W. (1946). Studies of Plasmodium cynomolgi in the rhesus monkey, Macaca mulatta. Am. J. Hyg. 44, 273300.Google ScholarPubMed
Zuckerman, Avivah (1953). Residual immunity following radical cure of Plasmodium berghei in intact and splenectomized voles (Microtus guentheri). J. infect. Dis. 92, 205–23.CrossRefGoogle ScholarPubMed