Yáñez M A, Coppola M P, Russo D A, Delaha E, Chaparas S D, Yeager H
J Clin Microbiol. 1986 May;23(5):822-5. doi: 10.1128/jcm.23.5.822-825.1986.
An enzyme-linked immunosorbent assay (ELISA) was examined for its usefulness in detecting mycobacterial antigens in sputum. A double-antibody sandwich procedure was set up by using a commercially available hyperimmune serum directed against Mycobacterium bovis, BCG. The ELISA was able to detect 10 ng of protein per ml of BCG sonic extract. The system also clearly distinguished Mycobacterium tuberculosis organisms from Mycobacterium avium and Mycobacterium kansasii organisms. A total of 68 unknown sputum specimens submitted to the clinical laboratories for examination for tuberculosis were tested by ELISA. Of the 20 specimens that were smear positive and culture positive, 12 (60%) were positive by ELISA; 6 of the 11 (55%) smear-positive culture-negative samples were positive by ELISA; 1 of 2 (50%) of the smear-negative culture-positive samples was positive by ELISA; and only 3 of 35 (9%) of the smear-negative culture-negative samples were positive by ELISA. This approach offers promise as an aid in the presumptive differentiation of nontuberculous mycobacteria from the M. tuberculosis complex.
对酶联免疫吸附测定(ELISA)检测痰液中分枝杆菌抗原的效用进行了研究。通过使用市售的针对牛分枝杆菌卡介苗(Mycobacterium bovis, BCG)的超免疫血清建立了双抗体夹心程序。ELISA能够检测出每毫升卡介苗超声提取物中10纳克的蛋白质。该系统还能清楚地区分结核分枝杆菌与鸟分枝杆菌和堪萨斯分枝杆菌。共有68份提交给临床实验室进行结核病检查的未知痰液标本通过ELISA进行了检测。在20份涂片阳性且培养阳性的标本中,12份(60%)通过ELISA呈阳性;11份涂片阳性培养阴性样本中的6份(55%)通过ELISA呈阳性;2份涂片阴性培养阳性样本中的1份(50%)通过ELISA呈阳性;而35份涂片阴性培养阴性样本中只有3份(9%)通过ELISA呈阳性。这种方法有望作为一种辅助手段,用于从结核分枝杆菌复合群中初步鉴别非结核分枝杆菌。