RESUMEN
The development of an enzyme-linked immunosorbent assay (ELISA) for the detection of Babesia ovis antibodies is described. In an initial study, a crude Babesia bovis antigen and a synthetic B. bovis-derived antigen (designated 11C5) were used to screen 46 B. ovis-positive and 55 negative sheep sera. A 95% correlation between the two antigenic preparations was found with the positive sera; no negative sera gave positive reactions. The synthetic antigen was then used in the screening of 1466 sera collected from sheep from 18 regions of Turkey. A high incidence of B. ovis-positive reactions was found from all regions (60-80%) in sheep over 1 year old, while from two smaller samples the incidence in young sheep was much less (28 and 52%). This test is superior to existing ones because the synthetic antigen can be produced in a highly reproducible state, is specific and is stable over extended periods of time.
Asunto(s)
Antígenos de Protozoos , Babesia bovis/inmunología , Babesiosis/diagnóstico , Ensayo de Inmunoadsorción Enzimática , Enfermedades de las Ovejas/diagnóstico , Animales , Reacciones Cruzadas , Valor Predictivo de las Pruebas , Proteínas Recombinantes , Reproducibilidad de los Resultados , Ovinos , TurquíaRESUMEN
Adult sheep were vaccinated twice with crude extracts of either Babesia bovis or B ovis parasites in Freund's complete adjuvant, four weeks apart. Three weeks later these two groups and a third susceptible group were challenged with B ovis organisms. Both vaccinated groups had significantly lower parasitaemias than control animals.