Gürsoy Nafia Canan, Yakupoğulları Yusuf, Tekerekoğlu Mehmet Sait, Otlu Barış
İnönü University Faculty of Medicine, Department of Medical Microbiology, Malatya, Turkey.
Mikrobiyol Bul. 2016 Apr;50(2):196-204. doi: 10.5578/mb.21033.
Rapid and accurate detection of active tuberculosis (TB) cases is one of the most important goal of tuberculosis control programme. For this purpose, new methods are being developed to isolate, serotype and determine the drug resistance of the agent. Xpert MTB/RIF test (CepheidGeneXpert® System, USA) that has been recently developed, is a real-time polymerase chain reaction-based method which detects Mycobacterium tuberculosis complex and resistance of the strain to rifampicin (RIF) from the clinical sample directly within a couple of hours. However, there are not sufficient data about the performance of that test for extrapulmonary samples and pulmonary samples other than sputum. The aims of this study were to investigate the sensitivity, specificity, positive and negative predictive values of Xpert MTB/RIF test in detection of M. tuberculosis and the performance in the determination of rifampicin resistance of the isolates from pulmonary and extrapulmonary clinical samples. A total of 2160 clinical samples, in which 1141 (52.8%) were pulmonary and 1019 (47.2%) were extrapulmonary samples, sent to our laboratory between July 2013 to December 2014, were included in the study. Sixty seven of the evaluated samples (3.1%) were positive with microscopy (acid-fast stain; AFS), 116 samples (5.1%) were positive with culture and 98 samples (4.5%) were positive with Xpert MTB/RIF test. When the culture was considered as the reference method, the sensitivity and specificity of Xpert MTB/RIF test were determined as 73.3% and 99.3%, respectively for all samples; 77.5% and 99.5%, respectively for pulmonary samples and 63.9% and 99.2%, respectively for extrapulmonary samples. Among AFS positive samples, the sensitivity was 100% and specificity was 66.7%; whereas among AFS negative samples those values were 40.4% and 99.4%, respectively. Among all the samples involved in the study, RIF resistance was determined only in three samples with Xpert MTB/ RIF test and that was also proved phenotypically (100% concordance). According to mycobacterial culture results, positive and negative predictive values of Xpert MTB/RIF test were determined as 86.7% and 98.5%, respectively for all samples. Those were determined as 92.5% and 98.3%, respectively for extrapulmonary samples and were determined as 74.2 and 98.7%, respectively for pulmonary samples. According to the results obtained in our study, sensitivity of Xpert MTB/RIF test for extrapulmonary samples was found to be at moderate level; sensitivity of the test was found to be decreased especially in AFS negative samples with less bacilli load. Nonetheless, specificity of Xpert MTB/RIF test to the agent in all samples was found to be extremely high. In our study, although RIF-resistant strains were detected in few of the samples, Xpert MTB/ RIF test could differentiate all resistant and sensitive strains. Additionally, detection of M. tuberculosis and RIF resistance in our laboratory takes approximately 20.96 days with culture, this period decreases to a couple of hours with Xpert MTB/RIF test. Because of the advantages such as being practical, rapid and requiring minimal safety measures, it was concluded that Xpert MTB/RIF test may contribute to rapid diagnosis of TB also in extrapulmonary samples, with the confirmation of culture method.
快速、准确地检测活动性肺结核病例是结核病控制规划的最重要目标之一。为此,正在开发新的方法来分离、进行血清分型并确定病原体的耐药性。最近开发的Xpert MTB/RIF检测(美国赛沛GeneXpert®系统)是一种基于实时聚合酶链反应的方法,可在数小时内直接从临床样本中检测结核分枝杆菌复合群以及菌株对利福平(RIF)的耐药性。然而,关于该检测方法对肺外样本和除痰液以外的肺部样本的性能数据并不充分。本研究的目的是调查Xpert MTB/RIF检测在检测结核分枝杆菌中的敏感性、特异性、阳性和阴性预测值,以及在确定来自肺部和肺外临床样本的分离株利福平耐药性方面的性能。2013年7月至2014年12月期间送至我们实验室的总共2160份临床样本纳入了本研究,其中1141份(52.8%)为肺部样本,1019份(47.2%)为肺外样本。评估的样本中有67份(3.1%)经显微镜检查(抗酸染色;AFS)呈阳性,116份样本(5.1%)培养呈阳性,98份样本(4.5%)Xpert MTB/RIF检测呈阳性。以培养作为参考方法时,Xpert MTB/RIF检测对所有样本的敏感性和特异性分别确定为73.3%和99.3%;对肺部样本分别为77.5%和99.5%,对肺外样本分别为63.9%和99.2%。在AFS阳性样本中,敏感性为100%,特异性为66.7%;而在AFS阴性样本中,这些值分别为40.4%和99.4%。在本研究涉及的所有样本中,仅通过Xpert MTB/RIF检测在3份样本中确定了RIF耐药性,并且在表型上也得到了证实(一致性为100%)。根据分枝杆菌培养结果,Xpert MTB/RIF检测对所有样本的阳性和阴性预测值分别确定为86.7%和98.5%。对肺外样本分别为92.5%和98.3%,对肺部样本分别为74.2%和98.7%。根据我们研究获得的结果,发现Xpert MTB/RIF检测对肺外样本的敏感性处于中等水平;该检测的敏感性尤其在杆菌载量较少的AFS阴性样本中有所降低。尽管如此,发现Xpert MTB/RIF检测对所有样本中病原体的特异性极高。在我们的研究中,虽然在少数样本中检测到了RIF耐药菌株,但Xpert MTB/RIF检测能够区分所有耐药和敏感菌株。此外,在我们实验室通过培养检测结核分枝杆菌和RIF耐药性大约需要20.96天,而通过Xpert MTB/RIF检测这一时期可缩短至数小时。由于具有实用、快速且所需安全措施最少等优点,得出结论认为,在培养方法的确认下,Xpert MTB/RIF检测也可能有助于肺外样本中结核病的快速诊断。