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Enzyme-linked immunosorbent assays for the measurement of specific antibodies in experimentally induced ovine toxoplasmosis

Published online by Cambridge University Press:  19 October 2009

R. A. Payne
Affiliation:
Public Health Laboratory, Singleton Hospital, Sketly, Swansea, SA2 8QA, Wales
D. H. M. Joynson
Affiliation:
Public Health Laboratory, Singleton Hospital, Sketly, Swansea, SA2 8QA, Wales
A. J. Wilsmore
Affiliation:
Department of Animal Health and Production, Royal Veterinary College, Potters Bar, Herts, England
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Summary

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Tachyzoitcs of the RH strain of Toxoplasma gondii were inoculated intravenously into sheep following which serum samples were collected at approximately weekly intervals for 9 months. The sera were examined by the toxoplasma dye test and two enzymc-linkcd immunosorbent assays (ELISA) specifically developed for investigations of ovine toxoplasmosis. One was an antibody class capture assay for the detection of anti-toxoplasma specific IgM, the other an indirect assay which detected anti-toxoplasma IgG.

Some of the sheep had antibodies to toxoplasma prior to inoculation but none had specific IgM. Sera collected 17 days after inoculation showed that all had raised specific antibody levels but the only sheep that produced specific antitoxoplasma IgM were those that were initially without any antibody. Specific IgM could be detected in all these particular sheep for at least 1 month after infection and up to 3 months in some. Specific IgG persisted at high levels for at least 3 months and could still be detected at moderate levels for at least 9 months. The ELISA methods described are simple to perform and could clearly distinguish between previous infection and this experimental infection with Toxoplasma gondii.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1988

References

REFERENCES

Balfour, A. H. & Harford, J. D. (1985). Detection of specific IgG and IgM antibodies to Toxoplasma gondii with a commercially available enzyme immunoassay kit system. Journal of Clinical Pathology 38, 679689.CrossRefGoogle ScholarPubMed
Blewett, D. A., Bryson, C. E., & Miller, J. K. (1983). Studies of antibody titres in experimentally induced ovine toxoplasmosis. Research in Veterinary Science 34, 163166.CrossRefGoogle ScholarPubMed
Cathie, T. A. B. (1957). An appraisal of the diagnostic value of the Herological tests for toxoplasmosis. Transactions of the Royal Society of Tropical Medicine ami Hygiene 51, 104111.CrossRefGoogle Scholar
Fleck, D. G. & Kwantes, W. (1980). The laboratory diagnosis of toxoplasmosis. Public Health Ijaltoratory Service Monograph 13, London: H.M.S.O.Google Scholar
Francis, J. M., Payne, R. A., & Joynson, D. H. M. (1987). The relationship of the dye test to an enzyme-linked irnmunosorbent assay for the detection of toxoplasma IgG. (Manuscript in preparation.)Google Scholar
Payne, R. A., Isaac, M. & Francis, , Janet, M. (1982). Enzyme-linked immunosorbent assay (ELISA) using antibody class capture for the detection of antitoxoplasma IgM. Journal of Clinical Pathology 35, 802890.Google Scholar
Payne, R. A., Joynson, D. H. M., Balfour, A., Harford, J. P., Fleck, D. G., Mythen, M. & Saundeus, R. J. (1987). The Public Health Laboratory Service enzyme-linked immunosorbent assay for the detection of toxoplasma specific IgM antibody. Journal of Clinical Pathology 40, 276281.CrossRefGoogle Scholar
Wilson, M. B. & Nakane, P. K. (1978). Recent developments in the periodatc method of conjugating horseradish peroxidase (HRPO) to antibodies. In Immunoflorescence and Related Techniques (ed. Knapp, W.), pp. 215224. Amsterdam: Elsevier.Google Scholar