Miller Janice M, Jenny Allen L, Payeur Janet B
United States Department of Agriculture, National Animal Disease Center, Agricultural Research Service, P.O. Box 70, Ames, IA 50010, USA.
Vet Microbiol. 2002 Jun 5;87(1):15-23. doi: 10.1016/s0378-1135(02)00027-5.
In the US eradication program for bovine tuberculosis, a definitive diagnosis depends on the isolation of Mycobacterium bovis. However, in some cases bacterial culture is unsuccessful, even though the tissue is considered suspicious by histopathology because granulomatous lesions and acid-fast organisms are present. The purpose of this study was to determine if polymerase chain reaction (PCR) tests on formalin-fixed tissue would successfully identify the organisms observed in suspect lesions from culture-negative animals. Diagnostic laboratory records were used to select paraffin blocks of tissue from 102 ruminants that had suspect microscopic lesions but no bacterial isolation. Sections from these blocks were examined with PCR primers for IS6110 to detect Mycobacterium tuberculosis complex infection, or with 16S ribosomal RNA and IS900 primers for detection of Mycobacterium avium. The PCR tests successfully identified a mycobacterial infection in 58 of 102 tissues, including 41 M. tuberculosis complex and 17 M. avium (11 subspecies paratuberculosis). These results demonstrate that PCR testing of formalin-fixed tissue, in combination with bacterial culture, may increase the effectiveness of laboratory diagnostic efforts to detect and identify the most common mycobacterial diseases of ruminants.
在美国根除牛结核病的计划中,明确诊断取决于牛分枝杆菌的分离培养。然而,在某些情况下,尽管组织经组织病理学检查因存在肉芽肿性病变和抗酸菌而被视为可疑,但细菌培养仍未成功。本研究的目的是确定对福尔马林固定组织进行聚合酶链反应(PCR)检测是否能成功鉴定出培养阴性动物可疑病变中观察到的微生物。利用诊断实验室记录,从102只反刍动物中选取有可疑微观病变但未分离出细菌的组织石蜡块。用针对IS6110的PCR引物检测这些组织切片,以检测结核分枝杆菌复合群感染,或用16S核糖体RNA和IS900引物检测鸟分枝杆菌。PCR检测在102个组织中的58个中成功鉴定出分枝杆菌感染,包括41个结核分枝杆菌复合群和17个鸟分枝杆菌(11个副结核亚种)。这些结果表明,福尔马林固定组织的PCR检测与细菌培养相结合,可能会提高实验室诊断工作检测和鉴定反刍动物最常见分枝杆菌病的有效性。