Conville P S, Keiser J F, Witebsky F G
Clinical Pathology Department, Warren G. Magnuson Clinical Center, National Institutes of Health, Bethesda, Maryland 20892.
Diagn Microbiol Infect Dis. 1989 Jul-Aug;12(4):309-13. doi: 10.1016/0732-8893(89)90095-3.
Three methods of concentrating 1 ml aliquots from BACTEC 13A bottles containing patient blood samples were evaluated for testing with the Gen-Probe Rapid Diagnostic System for Mycobacteria avium complex: 1. using no reagents, 2. using both lysing and wash reagents; and 3. using lysing reagent only. Aliquots from 13As containing human blood and seeded with eight mycobacterial species were also concentrated directly and using both reagents. Results for samples containing M. avium were as follows: 1. using the direct concentration technique 34 of 47 samples (72%) gave unequivocally positive results; 2. 43 of 47 samples (92%) concentrated using both reagents gave positive results; 3. the technique using lysing reagent only was not found useful. There were no false positives with any of the seeded specimens. We were also able to define the minimum Growth Index necessary to ensure un-equivocally positive results for each concentration technique. For those samples containing M. avium these values were 42 for the technique using both reagents and 86 for the direct technique. Direct or reagent concentration of 13A aliquots for testing with Gen-Probe DNA probes provides a rapid, sensitive, and specific means for the identification of M. avium complex bacteremia.
评估了三种从装有患者血样的BACTEC 13A瓶中浓缩1毫升等分试样的方法,用于使用Gen-Probe鸟分枝杆菌复合群快速诊断系统进行检测:1. 不使用试剂;2. 使用裂解和洗涤试剂;3. 仅使用裂解试剂。对含有人类血液并接种了八种分枝杆菌的13A瓶中的等分试样也进行了直接浓缩以及使用两种试剂进行浓缩。含有鸟分枝杆菌的样本结果如下:1. 使用直接浓缩技术,47个样本中有34个(72%)得到明确阳性结果;2. 使用两种试剂浓缩的47个样本中有43个(92%)得到阳性结果;3. 仅使用裂解试剂的技术未发现有用。接种的标本均无假阳性。我们还能够确定每种浓缩技术确保明确阳性结果所需的最低生长指数。对于那些含有鸟分枝杆菌的样本,使用两种试剂的技术该值为42,直接技术为86。用Gen-Probe DNA探针检测时,对13A瓶等分试样进行直接或试剂浓缩,为鉴定鸟分枝杆菌复合群菌血症提供了一种快速、灵敏且特异的方法。