RESUMEN
We conducted a seroepidemiological survey to determine the prevalence of caseous lymphadenitis (CLA) in goat herds in Minas Gerais state, Brazil. Serum samples were collected from goats (n=676) from 108 rural properties in 2001, covering most of the sub-regions of this ca. 586,500 square kilometer state. Antibodies against Corynebacterium pseudotuberculosis secreted proteins were detected by an indirect enzyme-linked immunosorbent assay (ELISA). Most of the animals (78.9%) tested positive for CLA; 98% of flocks presented at least one seropositive animal. Goats managed under an extensive production system had a significantly higher seroprevalence of CLA than those in intensive and semi-intensive operations. The age distribution of the animals in the flocks affected the prevalence of this disease; however, goat breed did not. We found seropositivity against C. pseudotuberculosis to be highly prevalent in these Brazilian goat herds; consequently, appropriate management practices for the control of CLA should be implemented.
Asunto(s)
Infecciones por Corynebacterium/veterinaria , Corynebacterium pseudotuberculosis , Enfermedades de las Cabras/diagnóstico , Linfadenitis/veterinaria , Animales , Proteínas Bacterianas/inmunología , Brasil/epidemiología , Infecciones por Corynebacterium/diagnóstico , Infecciones por Corynebacterium/epidemiología , Ensayo de Inmunoadsorción Enzimática/veterinaria , Femenino , Enfermedades de las Cabras/epidemiología , Enfermedades de las Cabras/microbiología , Cabras/microbiología , Linfadenitis/diagnóstico , Linfadenitis/epidemiología , Linfadenitis/microbiología , Masculino , Prevalencia , Estudios SeroepidemiológicosRESUMEN
LipL32 is the major lipoprotein in the membrane of pathogenic leptospira. In this work, we report on the production of monoclonal antibodies (MAbs) against recombinant LipL32 (rLipL32) and on the evaluation of their potential for use as reagents in diagnostic tests for leptospirosis. The MAbs were all of the IgG(2b) isotype and reacted specifically with native LipL32 in pathogenic serovars only. MAbs reacted in the same region of the rLipL32 molecule and their affinity constant was between 5x10(7) M(-1) and 6x10(6) M(-1). These results suggest that although the MAbs cannot be used together, they are well suited for diagnostic tests of leptospirosis based on LipL32 detection.