Department of Microbiology, Hospital Universitari de Bellvitge-IDIBELL, Hospitalet de Llobregat, Spain.
Department of Pathology and Experimental Therapy, Universitat de Barcelona, Hospitalet de Llobregat, Spain.
J Clin Microbiol. 2018 Aug 27;56(9). doi: 10.1128/JCM.00659-18. Print 2018 Sep.
The rapid detection of complex (MTUBC) in clinical samples is essential for successful treatment. New techniques such as real-time PCR have been developed in order to facilitate rapid diagnosis, but their sensitivity is low in extrapulmonary specimens, due to the low bacillary load in such samples. A next-generation assay has recently been developed to try to overcome this limitation. The aim of this study was to analyze the effectiveness of the Xpert MTB/RIF Ultra (GX-Ultra) for the detection of MTUBC DNA in 108 smear-negative extrapulmonary specimens that were MTUBC culture positive. In addition, 40 extrapulmonary culture-negative samples and 20 samples with nontuberculous mycobacteria were tested to evaluate the specificity of the assay. All samples were collected between May 1999 and May 2017. The GX-Ultra detected DNA of MTUBC in 82 extrapulmonary specimens that were MTUBC culture positive (75.9% sensitivity; 95% confidence interval [CI], 66.6 to 83.4%). The assay was negative for all clinical specimens that were MTUBC culture negative and the samples with nontuberculous mycobacteria (100% specificity). Furthermore, two (1.8%) samples presented mutations related to rifampin resistance. The highest sensitivity was obtained in samples of lymph nodes (94.1%) and nonsterile fluids (93.7%), followed by tissue specimens (86.6%), stool material (80%), abscess aspirates (64.7%), and sterile fluids (60.5%). Pleural fluids, one of the least optimal samples for detecting DNA of MTUBC, were GX-Ultra positive in 10/21 (47.6%) of cases. In summary, GX-Ultra showed excellent specificity and high sensitivity in paubacillary specimens, making it a useful tool for rapid diagnosis of extrapulmonary tuberculosis.
快速检测临床样本中的复杂分枝杆菌(MTUBC)对于成功治疗至关重要。为了便于快速诊断,已经开发了新的技术,如实时 PCR,但由于这些样本中的细菌负荷低,其在肺外标本中的灵敏度较低。最近开发了一种下一代检测方法来试图克服这一限制。本研究旨在分析 Xpert MTB/RIF Ultra(GX-Ultra)在 108 例 MTUBC 培养阳性的痰涂片阴性肺外标本中检测 MTUBC DNA 的有效性。此外,还测试了 40 例肺外培养阴性样本和 20 例非结核分枝杆菌样本,以评估该检测方法的特异性。所有样本均于 1999 年 5 月至 2017 年 5 月采集。GX-Ultra 在 82 例 MTUBC 培养阳性的肺外标本中检测到 MTUBC DNA(75.9%的敏感性;95%置信区间 [CI],66.6 至 83.4%)。该检测方法对所有 MTUBC 培养阴性的临床标本和非结核分枝杆菌样本均呈阴性(100%的特异性)。此外,有两个(1.8%)样本存在与利福平耐药相关的突变。在淋巴结(94.1%)和非无菌体液(93.7%)样本中获得了最高的敏感性,其次是组织标本(86.6%)、粪便材料(80%)、脓肿抽吸物(64.7%)和无菌体液(60.5%)。在检测 MTUBC DNA 方面,胸腔积液是最不理想的样本之一,在 21 例中的 10 例(47.6%)呈 GX-Ultra 阳性。总之,GX-Ultra 在低负荷样本中显示出出色的特异性和高灵敏度,是快速诊断肺外结核病的有用工具。