Kolk A H, Schuitema A R, Kuijper S, van Leeuwen J, Hermans P W, van Embden J D, Hartskeerl R A
N. H. Swellengrebel Laboratory of Tropical Hygiene, Royal Tropical Institute, Amsterdam, The Netherlands.
J Clin Microbiol. 1992 Oct;30(10):2567-75. doi: 10.1128/jcm.30.10.2567-2575.1992.
A test based on the polymerase chain reaction (PCR) was developed for the detection of the Mycobacterium tuberculosis complex in clinical samples. In this test, a 245-bp sequence of the insertion element IS986 was amplified and detected by agarose gel electrophoresis in the presence of ethidium bromide and by Southern blot and dot blot hybridization by using a 188-bp digoxigenin-labeled probe. We tested clinical specimens from 227 patients suspected of having tuberculosis. These included 102 cerebrospinal fluid, 48 sputum, 18 pleural fluid, 5 bronchoalveolar lavage, 18 blood, 7 pus, 8 bone marrow, and 6 urine samples and 15 tissue biopsy specimens. We also tested sputum samples from 75 patients with diseases other than tuberculosis. Sputum samples were first decontaminated, and all samples were treated with proteinase K-detergent solution to extract the DNA. Part of each sample was spiked with M. tuberculosis to provide a semiquantitative assay and to control for the loss of mycobacteria or interference with the PCR which may cause false-negative results. One femtogram of M. tuberculosis DNA could be detected. PCR was positive for all 32 culture-positive (for M. tuberculosis) and Ziehl-Neelsen staining (ZN)-positive samples, 10 of 12 culture-positive and ZN-negative samples, and all 4 culture-negative and ZN-positive samples. PCR detected M. tuberculosis complex bacteria in 35 of 178 culture- and ZN-negative samples. Clinical data supported the diagnosis of tuberculosis in the majority of the 35 patients from whom those samples were obtained.
开发了一种基于聚合酶链反应(PCR)的检测方法,用于检测临床样本中的结核分枝杆菌复合群。在该检测中,插入元件IS986的一段245 bp序列经扩增后,在溴化乙锭存在的情况下通过琼脂糖凝胶电泳进行检测,并使用188 bp地高辛标记探针通过Southern印迹和斑点印迹杂交进行检测。我们检测了227例疑似结核病患者的临床标本。这些标本包括102份脑脊液、48份痰液、18份胸腔积液、5份支气管肺泡灌洗样本、18份血液、7份脓液、8份骨髓、6份尿液样本以及15份组织活检标本。我们还检测了75例非结核疾病患者的痰液样本。痰液样本首先进行净化处理,所有样本均用蛋白酶K - 去污剂溶液处理以提取DNA。每个样本的一部分加入结核分枝杆菌以提供半定量检测,并控制分枝杆菌的损失或对可能导致假阴性结果的PCR的干扰。可检测到1飞克的结核分枝杆菌DNA。对于所有32份培养阳性(结核分枝杆菌)且萋 - 尼染色(ZN)阳性的样本、12份培养阳性且ZN阴性样本中的10份以及所有4份培养阴性且ZN阳性的样本,PCR检测均为阳性。PCR在178份培养及ZN阴性样本中的35份中检测到结核分枝杆菌复合群细菌。临床数据支持了从其获取这些样本的35例患者中大多数患者的结核病诊断。