Ren Fei, Ma JinBao, Dang LiYun, Li AiFang, Zhao GuoLian, Qi Yun, Xu You, Yang Han, Li JianYing
Department of Drug-Resistance Tuberculosis, Xi'an Chest Hospital, Xi'an, China.
Department of Clinical Laboratory, Xi'an Chest Hospital, Xi'an, Shaanxi Province, China.
BMC Infect Dis. 2024 Dec 28;24(1):1469. doi: 10.1186/s12879-024-10378-0.
This study evaluates the effectiveness of nanopore sequencing for accurate detection of Mycobacterium tuberculosis pathogens and drug resistance mutations in clinical specimens.
A retrospective analysis of 2,421 specimens from suspected tuberculosis patients admitted to Xi'an Chest Hospital from 2022 to 2023 was conducted, with 131 specimens undergoing via real-time, fluorescence-based quantitative Polymerase Chain Reaction (qPCR), simultaneous amplification and testing RNA (RNA), Mycobacterium culture, Mycobacterium smear, and nanopore sequencing. Employing clinical tuberculosis diagnoses as the gold standard, sensitivity, specificity, positive predictive value, negative predictive value, concordance rate, and Kappa coefficient were measured for the five detection techniques. We compared nanopore sequencing with the Melting Curve method to detect drug-resistant gene mutations.
Nanopore sequencing has a significantly higher sensitivity (0.786) for tuberculosis diagnosis compared to qPCR (0.411), RNA (0.411), Mycobacterium culture (0.402), and Mycobacterium smear (0.241), against the gold-standard clinical diagnosis. It also exhibited a greater concordance rate (0.809) and Kappa coefficient (0.488), and outperformed the other methods in terms of the area under the ROC curve. Nanopore sequencing surpassed the Melting Curve method in identifying drug-resistant mutations.
Nanopore sequencing significantly enhances the detection of tuberculosis pathogens and drug-resistant genes.
本研究评估纳米孔测序在准确检测临床标本中结核分枝杆菌病原体及耐药突变方面的有效性。
对2022年至2023年入住西安市胸科医院的疑似结核病患者的2421份标本进行回顾性分析,其中131份标本同时进行了基于实时荧光定量聚合酶链反应(qPCR)、RNA同步扩增检测(RNA)、分枝杆菌培养、分枝杆菌涂片及纳米孔测序。以临床结核病诊断为金标准,对这五种检测技术的灵敏度、特异度、阳性预测值、阴性预测值、符合率及Kappa系数进行测定。将纳米孔测序与熔解曲线法比较以检测耐药基因突变。
与qPCR(0.411)、RNA(0.411)、分枝杆菌培养(0.402)及分枝杆菌涂片(0.241)相比,纳米孔测序针对金标准临床诊断的结核病诊断灵敏度显著更高(0.786)。其符合率(0.809)和Kappa系数(0.488)也更高,且在ROC曲线下面积方面优于其他方法。在识别耐药突变方面,纳米孔测序优于熔解曲线法。
纳米孔测序显著提高了结核病原体及耐药基因的检测能力。