首页> 美国卫生研究院文献>Journal of Clinical Microbiology >False-Positive Gen-Probe Direct Mycobacterium tuberculosis Amplification Test Results for Patients with Pulmonary M. kansasii and M. avium Infections
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False-Positive Gen-Probe Direct Mycobacterium tuberculosis Amplification Test Results for Patients with Pulmonary M. kansasii and M. avium Infections

机译:堪萨斯肺炎和鸟分枝杆菌感染的假阳性Gen-Probe直接结核分枝杆菌扩增测试结果

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摘要

The Gen-Probe Amplified Mycobacterium Tuberculosis Direct (MTD) test has been approved for use in the United States for the rapid diagnosis of pulmonary tuberculosis in patients with acid-fast smear-positive sputum samples since 1996. Four patients infected with human immunodeficiency virus and one chronic pulmonary-disease patient seen in our institutions with abnormal chest radiographs and fluorochrome stain-positive sputa were evaluated for tuberculosis, including performance of the MTD test on expectorated sputum samples. Three of these five patients’ sputa were highly smear-positive (i.e., more than 100 bacilli per high-power field), while two patient’s sputa contained 1 to 10 bacilli per field. MTD results on sputum specimens from these patients ranged from 43,498 to 193,858 relative light units (RLU). Gen-Probe has defined values of at least 30,000 RLU as indicative of a positive test, i.e., the presence of Mycobacterium tuberculosis RNA. Four of the patients’ sputum cultures yielded growth of M. kansasii within 6 to 12 days, and the fifth produced growth of M. avium only. One patient’s culture contained both M. kansasii and M. avium, but none of the initial or follow-up cultures from these five patients revealed M. tuberculosis. However, subsequent cultures from three of the patients again revealed M. kansasii. During the period of this study, in which MTD tests were performed on smear-positive sputum specimens from 82 patients, four of seven patients with culture-proven M. kansasii pulmonary infections yielded one or more false-positive MTD tests. The MTD sensitivity observed in this study was 93.8%, and the specificity was 85.3%. Five cultures of M. kansasii (including three of these patients’ isolates and M. kansasii ATCC 12478), and cultures of several other species were examined at densities of 105 to 107 viable CFU/ml by the MTD test. All five isolates of M. kansasii and three of three isolates of M. simiae yielded false-positive test results, with readings of 75,191 to 335,591 RLU. These findings indicate that low-level false-positive MTD results can occur due to the presence of M. kansasii, M. avium, and possibly other Mycobacterium species other than M. tuberculosis in sputum. Low-level positive MTD results of 30,000 to 500,000 RLU should be interpreted in light of these findings. It remains to be determined if the enhanced MTD test (MTD 2) recently released by Gen-Probe will provide greater specificity than that observed in this report with its first-generation test.
机译:自1996年以来,Gen-Probe结核分枝杆菌直接扩增试验(MTD)已获准在美国用于快速诊断耐酸涂片阳性痰标本的患者的肺结核。四例患者感染了人类免疫缺陷病毒和我们对一名在我们机构中见过的胸部X光片和荧光染色阳性痰液异常的慢性肺病患者进行了结核病评估,包括对痰标本进行MTD测试。这五名患者的痰中有三名涂片阳性(即每个高倍视野中超过100个杆菌),而两名患者的痰中每个视野中含有1至10个细菌。这些患者的痰标本的MTD结果范围为43,498至193,858相对光单位(RLU)。 Gen-Probe具有至少30,000 RLU的定义值,可指示阳性测试,即结核分枝杆菌RNA的存在。患者的四份痰培养物在6至12天内产生了堪萨斯分枝杆菌的生长,而第五位仅产生了鸟分枝杆菌的生长。一名患者的培养物中同时含有堪萨斯分枝杆菌和鸟分枝杆菌,但是这五名患者的最初或后续培养均未发现结核分枝杆菌。然而,随后来自三名患者的培养再次显示了堪萨斯分枝杆菌。在本研究期间,对来自82位患者的涂片阳性痰标本进行了MTD测试,在经过培养证明的堪萨斯分枝杆菌肺部感染的7例患者中,有4例产生了一个或多个MTD测试为假阳性。在这项研究中观察到的MTD敏感性为93.8%,特异性为85.3%。在10 5 到10 7

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