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Demonstration of complement-fixation titres against the species-specific trachoma antigen in sera of trachoma patients

Published online by Cambridge University Press:  15 May 2009

A. L. Terzin
Affiliation:
Medical Faculty and HE Military Laboratory, Sarajevo, Yugoslavia
M. R. Fornazarić
Affiliation:
Medical Faculty and HE Military Laboratory, Sarajevo, Yugoslavia
B. V. Birtašević
Affiliation:
Medical Faculty and HE Military Laboratory, Sarajevo, Yugoslavia
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Semi-purified elementary body suspensions, prepared or preserved in three different ways, have been compared as to their species-specific CF-activity as revealed both against Bedsonia-negative sera of trachoma patients (of known stage), and against psittacosis-positive sera of men and animals.

Two of these antigens (the SPG-formol-antigen and the SPG-glycerol-antigen) revealed a positive species-specific CF-reaction in 61–100% of the Bedsonia-negative serum samples obtained from trachoma patients, with titres ranging from 1/2 to 1/128.

Various parameters (as percentage proportion of positive reactors, CF-titre, duration of the disease, clinical stage of trachoma, etc.) have been analysed for correlation, and the results obtained with the different antigens are compared with one another.

The most useful of the three antigens, showing a good species-specific CF-reactivity and no anticomplementary activity, was found to be the ‘SPG-formolantigen’. However because of its group-specific reactivity, for detection of species-specific trachoma antibodies in routine, it could be used only with Bedsonia-negative samples of sera. Because of the thermolability of its species-specific component, the SPG-formol-antigen proved to be liable to deterioration.

We have pleasure in thanking to Dr F. B. Gordon for help in procuring bibliography and the viable strain of trachoma virus. We wish to express our thanks also to Mrs R. Šepetavic and to Miss M. Krečo for their technical assistance.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1963

References

Bedson, S. P. (1936). Observations bearing on the antigenic composition of psittacosis virus. Brit. J. exp. Path. 17, 109.Google Scholar
Bedson, S. P. (1959). The Harben Lectures. The psittacosis-lymphogranuloma group of infective Agents. J. R. Inst. publ. Hlth, 22, 67.Google Scholar
Bernkoff, H. (1962). Discussion. Ann. N.Y. Acad. Sci. 98, 345.Google Scholar
Bovarnick, M. R., Miller, J. C. & Snyder, J. C. (1950). The influence of certain salts, amino acids, sugars and proteins on the stability of rickettsiae. J. Bact. 59, 509.CrossRefGoogle ScholarPubMed
Brand, G. & Keil, A. W. (1955). Konzentrierung von Komplementbindenden Influenza-Antigen durch Glyzerindialyse. Zbl. Bakt. (I., Abt. Orig.), 162, 12, 13.Google Scholar
Cabasso, V. J., Markham, F. S. & Cox, H. R. (1951). Stabilizing action of glycerine on hemagglutination of egg-adapted mumps, Newcastle disease and influenza viruses. Proc. Soc. exp. Biol., N.Y., 78, 791.CrossRefGoogle ScholarPubMed
Collier, L. H. (1961). Experiments with trachoma vaccines. Lancet, i, 795.CrossRefGoogle Scholar
Galton, M. M., Powers, D. K., Hall, A. D. & Cornell, R. G. (1958). A rapid macroscopicslide screening test for the serodiagnosis of Leptospirosis. Amer. J. vet. Res. 19, 71, 505.Google ScholarPubMed
Grayston, J. T., Wang, S. P., Woolridge, R. L., Yang, Y. F. & Johnston, P. B. (1960). Trachoma: studies of etiology, laboratory diagnosis and prevention. J. Amer. med. Ass. 172, 1577.CrossRefGoogle ScholarPubMed
Hanna, L. (1962). Isolation of trachoma and inclusion conjunctivitis viruses in the United States. Ann. N.Y. Acad. Sci. 98, 24.CrossRefGoogle ScholarPubMed
Murray, E. S., Guerra, P., Abbott, A. G. & McComb, D. E. (1962). Isolation of viruses of trachoma from patients in Ethiopia. Ann. N.Y. Acad. Sci. 98, 14.CrossRefGoogle ScholarPubMed
Snyder, J. C., Page, R. C., Murray, E. S., Daggy, R. H., Bell, S. D., Nichols, R. L., Haddad, N. A., Hanna, A. T. & McComb, D. (1959). Observations on the etiology of trachoma. Amer. J. Ophthal. 48, 325.CrossRefGoogle Scholar
Sowa, J. & Collier, L. H. (1960). Isolation of trachoma virus from patients in West Africa. J. Hyg., Camb., 58, 99.CrossRefGoogle ScholarPubMed
Terzin, A. L. (1953). Glycerine as a Stabilizer of some Complement-fixing antigens of viral and rickettsial origin. Proc. Soc. exp. Biol., N.Y., 84, 215.CrossRefGoogle ScholarPubMed
Terzin, A. L., Hlača, D. M. & Fornazarić, M. R. (1958). Antibodies against Bedsonia antigen in sera of animals. Arch. ges. Virusforsch., 8, 511.CrossRefGoogle Scholar
Terzin, A. L., Matuka, S., Fornazarić, M. R. & Hlača, D. M. (1961). Preparation of group-specific Bedsonia antigens for use in complement-fixation reactions. Acta Virol. 5, 78.Google Scholar
Terzin, A. L. & Birtašević, B. V. (1962). Complement-fixation and complement-fixation-inhibition titres against the Bedsonia antigen in sera of trachoma patients. J. Hyg., Camb., 60, 21.CrossRefGoogle ScholarPubMed
Woolridge, R. L. & Grayston, J. T. (1962). Further studies with a complement fixation test for trachoma. Ann. N.Y. Acad. Sci., 98, 314.CrossRefGoogle ScholarPubMed