Stabel J R
Zoonotic Diseases Research Unit, National Animal Disease Center, Ames, IA 50010, USA.
J Vet Diagn Invest. 1997 Oct;9(4):375-80. doi: 10.1177/104063879700900406.
A new method (NADC) for isolation of Mycobacterium paratuberculosis from fecal samples is described and evaluated using fecal samples from a known paratuberculosis-infected herd of cattle. The NADC method includes centrifugation of the total fecal sample supernatant and use of a 2-step decontamination protocol. The growth rate of M. paratuberculosis and contamination rate of cultures when using this method are compared to 3 other published methods: sedimentation, centrifugation, and Cornell. Sensitivity was lowest for the Cornell method precluding detection of some low shedders; however, contamination was not observed for this method. Contamination was the most severe in samples processed by the centrifugation method but was also high for the sedimentation method, resulting in unreadable culture tubes for some fecal samples. The NADC method was 10-fold more sensitive for detection of M. paratuberculosis colonies and contamination was significantly reduced compared to other 3 methods.
描述了一种从粪便样本中分离副结核分枝杆菌的新方法(NADC),并使用来自已知感染副结核病牛群的粪便样本进行了评估。NADC方法包括对粪便样本总上清液进行离心,并采用两步去污方案。将使用该方法时副结核分枝杆菌的生长速率和培养物的污染率与其他三种已发表的方法进行比较:沉降法、离心法和康奈尔法。康奈尔法的灵敏度最低,无法检测到一些低排泄量的样本;然而,该方法未观察到污染情况。离心法处理的样本污染最严重,但沉降法的污染也很高,导致一些粪便样本的培养管无法读数。与其他三种方法相比,NADC方法检测副结核分枝杆菌菌落的灵敏度高10倍,且污染显著减少。