靶向纳米孔测序技术鉴定结核分枝杆菌及其耐药性。

IF 1 Q3 BIOLOGY
Chen Tang, Feng Xu, Xiaoqun Zheng, Guangxin Xiang
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引用次数: 0

摘要

在传染病中,结核病仍然是人类死亡的主要原因。耐药结核病,特别是耐多药结核病和广泛耐药结核病,构成了一项紧迫的临床和公共卫生挑战。结核病的主要病原体是结核分枝杆菌(MTB),它表现出高度复杂的耐药谱。传统的基于培养的表型药敏检测耗时长,而基于pcr的检测仅限于检测已知的突变热点。在这项研究中,我们提出了一种利用高通量纳米孔测序技术与多重PCR相结合的方案,称为靶向纳米孔测序,用于MTB的鉴定和耐药性分析。我们的MTB耐药评估方法具有无培养、高效、高通量和高准确性等优点,可为临床患者管理和结核病感染控制提供重要帮助。•靶向纳米孔测序同时检测18个与结核分枝杆菌抗生素耐药性相关的基因。•该方法提供了14种一线和二线抗结核药物的广泛耐药谱,无需细菌培养。•该工艺的加速周转时间约为7.5 h,检测限为102个细菌/mL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Mycobacterium tuberculosis and its Drug Resistance by Targeted Nanopore Sequencing Technology.

Tuberculosis (TB) remains the leading cause of human mortality in infectious diseases. Drug-resistant TB, particularly multidrug-resistant TB and extensively drug-resistant TB, poses a pressing clinical and public health challenge. The main causative agents of TB are known as Mycobacterium tuberculosis (MTB), which exhibits a highly complex drug resistance profile. Traditional culture-based phenotypic drug susceptibility testing is time-consuming, and PCR-based assays are restricted to detecting known mutational hotspots. In this study, we present a protocol leveraging high-throughput nanopore sequencing technology in conjunction with multiplex PCR, termed targeted nanopore sequencing, for the identification of MTB and analysis of its drug resistance. Our method for MTB drug resistance assessment offers the benefits of being culture-free, efficient, high-throughput, and highly accurate, which could significantly aid in clinical patient management and the control of TB infections. Key features • Targeted nanopore sequencing detects 18 genes simultaneously linked to antibiotic resistance in MTB. • The method provides broad drug resistance profiles for 14 first- and second-line anti-TB drugs without bacterial culture. • The expedited turnaround time of the process is approximately 7.5 h with a detection limit of 102 bacteria/mL.

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