Analysis on Drug-Resistance-Associated Mutations among Multidrug-Resistant Mycobacterium tuberculosis Isolates in China

被引:8
作者
Jia, Hongbing [1 ,2 ]
Xu, Yuhui [3 ]
Sun, Zhaogang [1 ,2 ]
机构
[1] Beijing TB & Thorac Tumor Res Inst, Beijing Key Lab Drug Resistant TB Res, Beijing 101149, Peoples R China
[2] Capital Med Univ, Beijing Chest Hosp, Translat Med Ctr, Beijing 101149, Peoples R China
[3] China Acad Chinese Med Sci, Inst Chinese Mat Med, Beijing 100700, Peoples R China
来源
ANTIBIOTICS-BASEL | 2021年 / 10卷 / 11期
关键词
Mycobacterium tuberculosis; drug-susceptibility testing; multidrug resistance; mutation; MOLECULAR CHARACTERIZATION; ISONIAZID RESISTANCE;
D O I
10.3390/antibiotics10111367
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
As the causative bacteria of tuberculosis, Mycobacterium tuberculosis (M. tb) is aggravated by the emergence of its multidrug-resistant isolates in China. Mutations of six of the most frequently reported resistant genes (rpoB, katG, inhA, embB, gyrA, and rpsL) were detected for rifampicin (RIF), isoniazid (INH), ethambutol (EMB), ofloxacin (OFX), and streptomycin (STR) in this study. The amino acid missense mutations (MMs) and their corresponding single nucleotide polymorphism mutations for all drug-resistant (DR) isolates are described in detail. All isolates were divided into non-extensively drug-resistant (Non-XDR) and preXDR/XDR groups. No statistical differences were detected among MMs and linked MMs (LMs) between the two groups, except for rpsL 88 (p = 0.037). In the preXDR/XDR group, the occurrence of MMs in rpoB, katG, and inhA developed phenotypic resistance and MMs of rpoB 531, katG 315, rpsL 43, and rpsL 88 could develop high levels of DR. It is necessary to carry out epidemiological investigations of DR gene mutations in the local region, and thus provide necessary data to support the design of new technologies for rapid detection of resistant M. tb and the optimization of detection targets.
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页数:11
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