Zanini M S, Moreira E C, Lopes M T, Mota P, Salas C E
Departamento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Zentralbl Veterinarmed B. 1998 Oct;45(8):473-9. doi: 10.1111/j.1439-0450.1998.tb00818.x.
A simple method was developed for DNA extraction of Mycobacterium bovis in milk and further detection of the bacterium by polymerase chain reaction (PCR). Milk previously seeded with M. bovis was used as the starting material. The procedure involved overnight digestion of a milk sample with proteinase K at 56 degrees C and phenol extraction, followed by ethanol precipitation and PCR. The amplification pattern obtained was analyzed with primers BW8-BW9 which amplify a 248 bp in strains of M. bovis. By using the BW8-BW9 primers, 10(3) CFU were detected on silver-stained PAGE gels. The procedure was validated by PCR analysis of milk in tuberculin-positive animals. It is anticipated that this method can be used for routine diagnosis of M. bovis in milk samples.
开发了一种简单的方法用于从牛奶中提取牛分枝杆菌的DNA,并通过聚合酶链反应(PCR)进一步检测该细菌。预先接种了牛分枝杆菌的牛奶用作起始材料。该程序包括在56℃下用蛋白酶K对牛奶样品进行过夜消化和苯酚提取,然后进行乙醇沉淀和PCR。用引物BW8 - BW9分析获得的扩增模式,该引物在牛分枝杆菌菌株中扩增出248 bp的片段。通过使用BW8 - BW9引物,在银染的聚丙烯酰胺凝胶上检测到10(3) CFU。通过对结核菌素阳性动物的牛奶进行PCR分析验证了该程序。预计该方法可用于牛奶样品中牛分枝杆菌的常规诊断。