Standardization and utility of counterimmunoelectrophoresis for the diagnosis of bartonellosis

Descripción del Articulo

Introduction. Carrion’s disease, caused by the bacterium Bartonella bacilliformis, is a reemerging disease in Perú, which is conventionally diagnosed by blood smear and culture, which are not very sensitive methods, requiring alternative diagnostic methods. Objectives. To determine...

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Detalles Bibliográficos
Autores: Acuña, Dante, Cornejo, William
Formato: artículo
Fecha de Publicación:2020
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:ojs.csi.unmsm:article/18713
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/18713
Nivel de acceso:acceso abierto
Materia:Contrainmunoelectroforesis
Infecciones por Bartonella
Serología
Pruebas Inmunológicas
Antígenos
Sonicación
Counterimmunoelectrophoresis
Bartonella infections
Serology
Immunologic Tests
Antigens
Sonication
Descripción
Sumario:Introduction. Carrion’s disease, caused by the bacterium Bartonella bacilliformis, is a reemerging disease in Perú, which is conventionally diagnosed by blood smear and culture, which are not very sensitive methods, requiring alternative diagnostic methods. Objectives. To determine the sensitivity and specificity of the counterimmunoelectrophoresis (CIEP) using a sonicated antigen obtained from a Bartonella sp. strain, to detect antibodies against the bacteria compared to the culture as reference standard. Methods. The test antigen was obtained by sonication of an isolate of Bartonella sp., grown in a biphasic medium with and without sheep blood. The reactivity of the sonic antigen was evaluated by the CIEP using 123 sera from people, of which 60 were from patients with a clinical and bacteriological diagnosis of Carrión’s disease, 54 from people with other infections and 9 from healthy people. For the standardization of the CIEP test, the size and distance between the wells were evaluated, as well as the concentration of the antigen and the volumes of the reagents used. Results. The optimal concentration of the antigen was 0,64 mg/mL, the distance between the 3 mm wells, the size of the 3 mm wells and the volume of the reagents of 12 μL. The standardized CIEP had a sensitivity of 43,3% and a specificity of 98,4%. Conclusions. The results of the CIEP reveal a low sensitivity of the test, being able to be used as a confirmatory test given its high specificity but cannot be used as a serological screening test due to the low sensitivity referred to.
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