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Immunologic Analysis by Quantitative Fluorescent Antibody Methods of the Effects of Prolonged Cultivation on Trichomonas gallinae* |
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| Authors: | B M HONIGBERG MORRIS GOLDMAN Portia A Holt |
| Institution: | 1. U. S. Department of Health, Education and Welfare, Public Health Service, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Laboratory of Parasitic Diseases, Bethesda, Maryland 20014
Special Research Fellow (1F3 AI28, 491–01), U. S. Public Health Service, and Guest Investigator, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, 1965/66. Permanent address: Department of Zoology, University of Massachusetts, Amherst, Mass. 01002.;2. U. S. Department of Health, Education and Welfare, Public Health Service, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Laboratory of Parasitic Diseases, Bethesda, Maryland 20014 Bionetics Research Laboratories, Kensington, Maryland 20795.;3. U. S. Department of Health, Education and Welfare, Public Health Service, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Laboratory of Parasitic Diseases, Bethesda, Maryland 20014 |
| Abstract: | SYNOPSIS. Antisera were developed in rabbits against homogenized antigens prepared from 3 axenic lines of Trichomonas gallinae: JB(VI), the 6th isolate of the very virulent Jones' Barn strain which was kept frozen in liquid nitrogen and was fully pathogenic for pigeons at the time at which it was employed for immunization; JB (VI)C, a substrain derived from JB(VI), but attenuated during continuous in vitro cultivation for 1 year; and JB(V)C, a substrain of the 5th isolate of the Jones' Barn strain attenuated during continuous in vitro cultivation for over 3 years. Globulin fractions of the antisera were conjugated with fluorescein isothiocyanate (FITC), and fractionated on DEAE-cellulose columns to yield highly specific fractions. Intact, formalin-fixed flagellates of each line were stained on slides with each labelled antiserum under standardized conditions. Fluorescence emitted by individual organisms was measured with the aid of a special microfluorimetric apparatus. Experiments involving direct staining, one-step inhibition, and cross-absorption methods indicated the presence of unique and cross-reacting antigenic systems in each of the 3 lines of trichomonads. The 2 substrains attenuated in the course of prolonged in vitro cultivation, altho antigenically similar, could be readily differentiated from each other. Further, both of them appeared to contain more antigenic systems than the still fully virulent JB(VI) parasites. |
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