Institute of Veterinary Bacteriology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
J Dairy Sci. 2013 Jun;96(6):3611-20. doi: 10.3168/jds.2012-6124. Epub 2013 Apr 12.
Bovine mastitis, an inflammatory disease of the mammary gland, is one of the most costly diseases affecting the dairy industry. The treatment and prevention of this disease is linked heavily to the use of antibiotics in agriculture and early detection of the primary pathogen is essential to control the disease. Milk samples (n=67) from cows suffering from mastitis were analyzed for the presence of pathogens using PCR electrospray-ionization mass spectrometry (PCR/ESI-MS) and were compared with standard culture diagnostic methods. Concurrent identification of the primary mastitis pathogens was obtained for 64% of the tested milk samples, whereas divergent results were obtained for 27% of the samples. The PCR/ESI-MS failed to identify some of the primary pathogens in 18% of the samples, but identified other pathogens as well as microorganisms in samples that were negative by culture. The PCR/ESI-MS identified bacteria to the species level as well as yeasts and molds in samples that contained a mixed bacterial culture (9%). The sensitivity of the PCR/ESI-MS for the most common pathogens ranged from 57.1 to 100% and the specificity ranged from 69.8 to 100% using culture as gold standard. The PCR/ESI-MS also revealed the presence of the methicillin-resistant gene mecA in 16.2% of the milk samples, which correlated with the simultaneous detection of staphylococci including Staphylococcus aureus. We demonstrated that PCR/ESI-MS, a more rapid diagnostic platform compared with bacterial culture, has the significant potential to serve as an important screening method in the diagnosis of bovine clinical mastitis and has the capacity to be used in infection control programs for both subclinical and clinical disease.
奶牛乳腺炎是一种乳腺炎症性疾病,是影响奶牛养殖业的最昂贵疾病之一。这种疾病的治疗和预防与农业中抗生素的使用密切相关,早期检测主要病原体对于控制疾病至关重要。使用 PCR 电喷雾电离质谱(PCR/ESI-MS)分析了患有乳腺炎的奶牛的牛奶样本(n=67),以检测病原体,并将结果与标准培养诊断方法进行了比较。对 64%的测试牛奶样本进行了同步鉴定,而 27%的样本得到了不同的结果。PCR/ESI-MS 未能识别出 18%样本中的一些主要病原体,但也鉴定出了其他病原体以及培养阴性样本中的微生物。PCR/ESI-MS 可识别出混合细菌培养物样本中的细菌种属以及酵母和霉菌(9%)。使用培养物作为金标准,PCR/ESI-MS 对最常见病原体的敏感性范围为 57.1%至 100%,特异性范围为 69.8%至 100%。PCR/ESI-MS 还揭示了 16.2%的牛奶样本中存在耐甲氧西林基因 mecA,这与金黄色葡萄球菌等葡萄球菌的同时检测相关。我们证明,与细菌培养相比,PCR/ESI-MS 是一种更快速的诊断平台,具有作为牛临床乳腺炎重要筛查方法的巨大潜力,并具有用于亚临床和临床疾病感染控制计划的能力。