Standardization and application of indirect ELISA for diagnosis of Mycoplasma bovis in bovine blood serum samples

• Autor(a) principal: de Mesquita, Samira Moraes Cunha
• Data de Publicação: 2015
• Outros Autores: Mansur, Felipe Jansen, do Nascimento, Elmiro Rosendo, Barreto, Maria Lúcia, Kimura, Leda Maria Silva
• Tipo de documento: Artigo
• Idioma: por
• Título da fonte: Brazilian Journal of Veterinary Medicine
• Texto Completo: https://rbmv.org/BJVM/article/view/383
• topic: Mycoplasma bovis; imunógeno; ELISA; soro sanguíneo; Mycoplasma bovis; immunogen; ELISA; blood serum

ABSTRACT. Mesquita S.M.C., Mansur F.J., Nascimento E.R., Barreto M.L. & Kimura L.M.S. [Standardization and application of indirect ELISA for diagnosis of Mycoplasma bovis in bovine blood serum samples.] Padroniza- ção e aplicação de ELISA indireto para diagnóstico de Mycoplasma bovis em amostras de soro sanguíneo bovino. Revista Brasileira de Medicina Veterinária, 37(2):101-107, 2015. Universidade Federal Fluminense, Faculdade de Veteriná- ria, Rua Vital Brazil Filho, 64, Vital Brazil, Niterói, RJ 24230-340, Brasil. E-mail: [e-mail] International researchers presented results indicating frequent involvement of Mycoplasma spp. as a causative agent of mastitis in cattle, associating its presence with significant economic losses to farmers. Mycoplasma bovis is the species most reported and relevant, because it causes more severe disease. The level of antibodies against M. bovis remains high for several months and can be detected by ELISA. The aim of this work was to develop an indirect ELISA with whole cell antigen of M. bovis (strain Donetta PG 45) with subsequent application in bovine blood serum samples for detection of antibodies against M. bovis. The immunization of cows A and B by inoculating an immunogen against M. bovis to obtain hyperimmune blood serum was the first stage of this work, then the stage of standardization of ELISA was proceeded. The concentration of 2 mg of antigen/mL for coating the microtiter plates was decided by statistical analyses. The optical density value 0,2 was determined as the limit of reactivity discrimination of samples (the cut-off point). The hyperimmune blood serum sample of the cow A (collected 30 days after immunization) was chosen as the positive control and, the fetal calf serum was chosen as negative control of the assay. In addition, the ideal optimal dilutions found for blood serum samples was 1:400 and for conjugate was 1:10.000 and the substrate used was the ortho-phenylenediamine. The amount of 321 samples of cow blood serum from 15 farms was obtained for the application of the standardized indirect ELISA. It was diagnosed animals that have been exposed to M. bovis and the prevalence rate found in blood serum samples was 3,1% (10/321) and 46,7% (7/15) was the prevalence rate found between the corresponding farms studied.