Heller M, Berthold E, Pfützner H, Leirer R, Sachse K
Federal Health Office, Institute for Veterinary Medicine, Jena, Germany.
Vet Microbiol. 1993 Oct;37(1-2):127-33. doi: 10.1016/0378-1135(93)90187-c.
An enzyme-linked immunosorbent assay (ELISA) using a monoclonal antibody (mAb) was developed to detect Mycoplasma (M.) bovis in milk samples from cattle. With this procedure, 1 x 10(5) colony forming units per ml (cfu/ml) milk were routinely detectable. No cross-reactions to other bovine mycoplasma species were observed. Both the sensitivity of 80.6% and the specificity of 94.9% are sufficient for its use in diagnosis of clinical mastitis. The sensitivity could be increased by 10% after introduction of 48-hour pre-incubation of samples. This allowed recognition of cows shedding M. bovis amounts of 10(3) cfu/ml in their milk, which is typical for subclinical cases. Screening of milk samples by means of this antigen capture ELISA has advantages over culture methods in terms of speed and potential to monitor large herds, thereby permitting early culling of infected animals to reduce transmission of the pathogen to non-infected animals.
开发了一种使用单克隆抗体(mAb)的酶联免疫吸附测定(ELISA)法,用于检测牛的牛奶样本中的牛支原体(M. bovis)。采用该方法,每毫升牛奶中1×10⁵ 菌落形成单位(cfu/ml)通常可检测到。未观察到与其他牛支原体物种的交叉反应。80.6%的灵敏度和94.9%的特异性足以用于临床乳腺炎的诊断。样品预温育48小时后,灵敏度可提高10%。这使得能够识别牛奶中牛支原体含量为10³ cfu/ml的奶牛,这是亚临床病例的典型情况。通过这种抗原捕获ELISA法筛选牛奶样本,在速度和监测大群体的潜力方面比培养方法具有优势,从而允许早期淘汰感染动物,以减少病原体向未感染动物的传播。