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The secreted and somatic proteinases of the bovine lungworm Dictyocaulus viviparus and their inhibition by antibody from infected and vaccinated animals

Published online by Cambridge University Press:  06 April 2009

C. Britton
Affiliation:
Wellcome Laboratories for Experimental Parasitology, University of Glasgow
D. P. Knox
Affiliation:
Moredun Research Institute, Edinburgh
G. J. Canto
Affiliation:
Department of Veterinary Parasitology, University of Glasgow, Glasgow
G.M. Urquhart
Affiliation:
Department of Veterinary Parasitology, University of Glasgow, Glasgow
M. W. Kennedy
Affiliation:
Wellcome Laboratories for Experimental Parasitology, University of Glasgow

Summary

Proteinase activities were examined in extracts and excretory–secretory (ES) products of the infective and adult stages of the cattle lungworm, Dictyocaulus viviparus. Multiple enzyme activities were identified from each source, as defined by pH optima, substrate specificities, inhibitor effects and substrate gel electrophoresis. Serine-, cysteine- and metalloproteinases were identified, secreted materials being more active against protein substrates per unit protein than were extracts, and the particular proteinases produced varied with the developmental stage of the parasite. The antigenicity of these parasite proteinases was demonstrated by the inhibition of enzymic activity with Protein G-purified serum IgG antibody from both infected and vaccinated hosts and in the retardation of enzyme migration on electrophoresis of enzyme–antibody complexes. For the adult products, this confirmed that the enzymes concerned were of parasite origin, and not host-derived. These results argue for investigation of D. viviparus proteinases as targets for the antibody response in the limitation of parasite-mediated tissue damage and as the active principle behind the anti-D. viviparus vaccine.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1992

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References

REFERENCES

Commins, M. A., Goodger, B. V. & Wright, I. G. (1985). Proteinases in the lysate of bovine erythrocytes infected with Babesia bovis: Initial vaccination studies. International Journal for Parasitology 5, 491–5.Google Scholar
Cox, G. N., Pratt, D., Hageman, R. & Boisvenue, R. J. (1990). Molecular cloning and primary sequence of a cysteine protease expressed by Haemonchus contortus adult worms. Molecular and Biochemical Parasitology 41, 2534.CrossRefGoogle ScholarPubMed
Eakin, A. E., Bouvier, J., Sakanari, J. A., Craik, C. S. & McKerrow, J. H. (1990). Amplification and sequencing of genomic DNA fragments encoding cysteine proteases from protozoan parasites. Molecular and Biochemical Parasitology 39, 18.CrossRefGoogle ScholarPubMed
Jarrett, W. F. H., Jennings, F. W., Mcintyre, W. I. M. & Mulligan, W. (1957). The natural history of parasitic bronchitis with notes on prophylaxis and treatment. Veterinary Record 69, 1329–37.Google Scholar
Jarrett, W. F. H., Jennings, F. W., Mcintyre, W. I. M., Mulligan, W., Sharp, N. C. C. & Urquhart, G. M. (1959). Immunological studies on Dictyocaulus viviparus infection in calves. Double vaccination with irradiated larvae. American Journal of Veterinary Research 20, 522–6.Google Scholar
Jarrett, W. F. H., Jennings, F. W., Mcintyre, W. I. M., Mulligan, W. & Urquhart, G. M. (1955). Immunological studies on Dictyocaulus viviparus infection. Passive immunisation. Veterinary Record 67, 291–6.Google Scholar
Jarrett, W. F. H., Jennings, F. W., Mcintyre, W. I. M., Mulligan, W. & Urquhart, G. M. (1958). Irradiated helminth larvae in vaccination. Proceedings of the Royal Society of Medicine 51, 743–4.Google Scholar
Jarrett, W. F. H., Jennings, F. W., Mcintyre, W. I. M., Mulligan, W. & Urquhart, G. M. (1960). Immunological studies on Dictyocaulus viviparus infection. Immunity produced by the administration of irradiated larvae. Immunology 3, 145–51.Google ScholarPubMed
Kennedy, M. W. & Qureshi, F. (1986). Stage-specific secreted antigens of the parasitic larval stages of the nematode Ascaris. Immunology 58, 515–22Google Scholar
Knox, D. P. & Kennedy, M. W. (1988). Proteinases released by the parasitic larval stages of Ascaris suum and their inhibition by antibody. Molecular and Biochemical Parasitology 28, 207–16.Google Scholar
DeMartino, G. N. (1989). Purification of proteolytic enzymes. In Proteolytic Enzymes: A Practical Approach (ed. Richwood, D. & Hames, B. D.), pp. 1523. Oxford, New York and Tokyo: IRL Press.Google Scholar
McKerrow, J. H., Brindley, P., Brown, M., Gam, A. A., Staunton, C. & Neva, F. A. (1990). Strongyloides stercoralis: Identification of a protease that facilitates penetration of skin by infective larvae. Experimental Parasitology 70, 134–43.CrossRefGoogle ScholarPubMed
McKerrow, J. H. & Doenhoff, M. J. (1988). Schistosome proteases. Parasitology Today 4, 334–40.CrossRefGoogle ScholarPubMed
Newport, G., McKerrow, J. H., Barr, P. & Agabain, N. (1987). Stage specific expression of schistosome proteases. In Molecular Strategies of Parasitic Invasion (ed. Agabain, N., Goodman, H. & Noguiera, N.), pp. 121131. New York: Alan R. Liss, Inc.Google Scholar
Rege, A. A., Song, C-Y., Bos, H. J. & Dresden, M. H. (1989). Isolation and partial characterisation of a potentially pathogenic cysteine proteinase from adult Dictyocaulus viviparus. Veterinary Parasitology 34, 95102.CrossRefGoogle ScholarPubMed
Rubin, R. & Weber, T. B. (1955). Acquired resistance to Dictyocaulus viviparus, the lungworm of cattle. Preliminary report. Proceedings of the Helminthological Society of Washington 22, 124–9.Google Scholar
Sakanari, J. A., Staunton, C. E., Eakin, A. E., Craik, C. S. & McKerrow, J. H. (1989). Serine proteases from nematode and protozoan parasites: Isolation and sequence homologues using generic molecular probes. Proceedings of the National Academy of Sciences, USA 86, 15.Google Scholar
Starkey, P. M. & Barrett, A. J. (1979). Alpha-2- macroglobulin, a physiological regulator of proteinase activity. In Proteinases in Mammalian Cells and Tissues (ed. Barrett, A. J.), pp. 663–95. Amsterdam, New York and Oxford: North-Holland Publishing Co.Google Scholar
Wertheim, G., Lustigman, S., Silberman, H. & Shoshan, S. (1983). Demonstration of collagenase activity in adult Strongyloides ratti (Nematoda: Strongyloididae) and its absence in the infective larvae. Journal of Helminthology 57, 241–6.Google Scholar