Hostname: page-component-7c8c6479df-r7xzm Total loading time: 0 Render date: 2024-03-28T20:46:18.781Z Has data issue: false hasContentIssue false

Passively and actively acquired antibodies for Trichomonas foetus in very young calves

Published online by Cambridge University Press:  15 May 2009

W. R. Kerr
Affiliation:
Ministry of Agriculture Northern Ireland
Muriel Robertson
Affiliation:
Lister Institute, London S. W. 1
Rights & Permissions [Opens in a new window]

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

1. The normal agglutinin (n.a.) for Trichomonas foetus found in all normal adult cattle has a titre of 1:48 to 1:96. N.a. appears to be specific for T. foetus and cannot be absorbed by other flagellates such as T. vaginalis or even completely by the heterologous serological variety of T. foetus itself. The n.a. appears to be a native constituent of the serum and not to be induced by an exogenous antigen.

2. The n.a. passes into the serum of the calf from the maternal colostrum during the first 24 hr. of life. The elimination of the passive n.a. and the development of the autogenous newly formed n.a. in the calf are traced. The passive n.a. disappeared from the 17th to the 55th day and the autogenous n.a. began to appear as a rule from the 35th to the 60th day and was fully established by the 63rd to the 113th day.

3. The elimination of the maternal, induced antibody acquired passively from the colostrum took place logarithmically. The rate measured by the half-life ranged from 14 to 20 days, but in one animal which took a very large amount of colostrum it was 57 days.

4. The intramuscular injection of T. foetus antigen into very young calves up to 4 weeks old induced no antibody. When the doses were relatively small the animal produced antibody to antigen given at a later period. When a very large amount was injected in this early period the subsequent capacity to respond to the same antigen but not to other antigens was seriously impaired.

The personal encouragement of Prof. H. G. Lamont and the support afforded by the Ministry of Agriculture, Northern Ireland, are gratefully acknowledged.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1954

References

REFERENCES

Barr, M., Glenny, A. T. & Howie, J. W. (1953). J. Path. Bact. 65, 155.CrossRefGoogle Scholar
Burnet, F. M. & Fenner, F. (1949). Production of Antibodies, 2nd ed. Melbourne: Macmillan and Co.Google Scholar
Comline, R. S., Roberts, H. E. & Titchen, D. A. (1951 a). Nature, Lond., 167, 561.CrossRefGoogle Scholar
Comline, R. S., Roberts, H. E. & Titchen, D. A. (1951 b). Nature, Lond., 168, 84.CrossRefGoogle Scholar
Dixon, F. J., Talmage, D. W., Maurer, P. H. & Deichmüller, M. (1952). J. exp. Med. 96, 313.CrossRefGoogle Scholar
Dixon, F. J. & Maurer, P. H. (1953). (Abstracts), 4th Int. Congr. Microbiol., Rome 1953. pp. 320. vol. 1.Google Scholar
Feinberg, J. G. & Morgan, W. T. J. (1953). Brit. J. exp. Path. 34, 104.Google Scholar
Felton, L. D. (1949). J. Immunol. 61, 107.CrossRefGoogle Scholar
Howe, P. E. (1921). J. biol. Chem. 49, 115.CrossRefGoogle Scholar
Kerr, W. R. & Robertson, M. (1941). Vet. J. 97, 351.Google Scholar
Kerr, W. R. & Robertson, M. (1945). Vet. Rec. 57, 221.Google Scholar
Kerr, W. R. & Robertson, M. (1946). J. comp. Path. 54, 38.CrossRefGoogle Scholar
Pedersen, K. O. (1945). Ultracentrifuge Studies on Serum and Serum Fractions. Upsala.Google Scholar
Pierce, A. E. (1947). Lab. J. 8, 238.Google Scholar
Smith, E. L. & Holm, A. (1948). J. biol. Chem. 175, 349.CrossRefGoogle Scholar
Taliaferro, W. H. & Taliaferro, L. G. (1951). J. infect. Dis. 89, 143.CrossRefGoogle Scholar