Cousins D V, Evans R J, Francis B R
Animal Health Laboratories, Department of Agriculture, South Perth, Western Australia.
Aust Vet J. 1995 Dec;72(12):458-62. doi: 10.1111/j.1751-0813.1995.tb03489.x.
The BACTEC radiometric culture method for detection of Mycobacterium paratuberculosis was evaluated on faeces from cattle on a farm in quarantine for Johne's disease. A multiplex polymerase chain reaction (PCR) based on the IS900 sequence specific for M paratuberculosis and a genus specific 16S rRNA region was developed and used to test cultures showing evidence of mycobacterial growth in the BACTEC liquid radiometric culture medium. Using the BACTEC-PCR combination, confirmation of M paratuberculosis from faeces and tissue of clinically affected animals was achieved within 2 to 4 weeks and 1 week, respectively, a substantial improvement on traditional culture and identification methods. The PCR provided rapid exclusion of M paratuberculosis when other Mycobacterium spp were grown. The radiometric culture medium proved to be very sensitive for culturing Mycobacterium spp.
采用BACTEC放射测量培养法对一个因副结核病而处于检疫期的农场的牛粪便中的副结核分枝杆菌进行检测。开发了一种基于副结核分枝杆菌特异性IS900序列和属特异性16S rRNA区域的多重聚合酶链反应(PCR),并用于检测在BACTEC液体放射测量培养基中显示有分枝杆菌生长迹象的培养物。使用BACTEC-PCR联合方法,分别在2至4周和1周内从临床受影响动物的粪便和组织中确认了副结核分枝杆菌,这比传统培养和鉴定方法有了显著改进。当培养出其他分枝杆菌属细菌时,PCR可快速排除副结核分枝杆菌。结果证明,该放射测量培养基对培养分枝杆菌属细菌非常敏感。