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Detection of Mycoplasma bovis in Preservative-Treated Field Milk Samples

机译:防腐剂处理过的牛奶样品中牛支原体的检测

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摘要

Control of mycoplasmal mastitis requires individual cow milk sampling for culture and identification of My- co Plasma bovis. This sampling is time-consuming and expensive. Currently, some herds sample cows monthly with the dairy herd improvement (DHI) program, but a preservative is added to this milk that kills M bovis. In this paper, a nested polymerase chain reaction (PCR) procedure that allows for rapid testing of preservative- treated milk is validated. The specificity of the nested PCR assay was confirmed by testing isolated nucleic acids of other organisms phylogenetically related to M bovis or common to milk. A comparison against blind- passage culture on 53 field milk samples determined its sensitivity. Exposure of seeded milk samples to the procedure resulted in a sensitivity of 5. 1 cf u equivalents per milliliter. Analysis of these results proved that the nested PCR assay was as sensitive as traditional cul- ture and can be used on preservative-treated milk.
机译:要控制支原体性乳腺炎,需要单独取样牛奶以培养和鉴定牛原性肌原浆。这种采样既费时又昂贵。目前,有些牛群每月通过奶牛改良计划(DHI)对奶牛进行采样,但这种牛奶中添加了防腐剂,可以杀死牛牛。在本文中,通过嵌套聚合酶链反应(PCR)程序可以对经过防腐剂处理的牛奶进行快速测试,这一方法已得到验证。巢式PCR分析的特异性通过测试与牛源M牛相关或牛奶常见的其他生物的分离核酸得到确认。与对53个田间牛奶样品进行盲传培养的比较确定了它的敏感性。将种子奶样品暴露于该程序会导致灵敏度为5. 1 cf u当量/毫升。对这些结果的分析证明,巢式PCR检测与传统培养一样灵敏,可用于经过防腐剂处理的牛奶。

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