贵州省结核分枝杆菌贝达喹啉敏感性及分子突变特征

M D Wang, F Q Xia, X J Cao, T T Ren, W Z Ou, X L Yang, W Qin, J Huang
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引用次数: 0

摘要

目的:检测结核分枝杆菌(MTB)对新药贝达喹啉(Bdq)的耐药性及耐药相关基因的突变情况,分析耐药基因突变类型与耐药表型的相关性。方法:收集2020年1月至2022年12月贵阳市公共卫生临床中心鉴定的结核分枝杆菌521株,其中药敏结核(DS-TB) 253株,耐多药结核(MDR-TB) 268株。采用微孔板法检测结核分枝杆菌的常规药敏和Bdq的最低抑菌浓度(MIC)。同时,采用Sanger测序法鉴定所有菌株中Bdq耐药相关基因Rv0678、atpE和pepQ的突变,并对Bdq耐药菌株进行全基因组测序,分析其耐药及分子突变特征。结果:521株临床菌株Bdq MIC主要集中在0.016 ~ 0.12 mg/L范围内。bdq耐药菌株仅在MDR菌株中检出,耐药率为4.1%(11/268)。在11株Bdq表型耐药菌株中检测到已知Bdq耐药基因突变,其中10株为Rv0678基因突变,1株为Rv0678和pepQ基因突变,未检测到atpE基因突变。Rv0678基因共有8种突变类型,分别为C151T(3/11)、19delG(2/11)、G404A(1/11)、T284C(1/11)、C305T(1/11)、G149A(1/11)、T95C(1/11)和201delG(1/11)。调查发现,11例Bdq耐药患者中仅有1例有Bdq用药史;此外,对Bdq耐药菌株进行全基因组序列分析发现,3株菌株为聚集性菌株,表明传播是Bdq耐药的重要原因。结论:Bdq在贵州地区具有较强的抗菌活性。Rv0678基因突变是Bdq抗性的主要决定因素;传播对bdq抗性菌株的传播起着重要作用。这些发现强调了在控制耐多药结核病中需要进行Bdq耐药相关的遗传筛查和传播链监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Bedaquiline susceptibility and molecular mutation characteristics of Mycobacterium tuberculosis in Guizhou Province].

Objective: To detect the drug resistance of Mycobacterium tuberculosis (MTB) to the new drug bedaquiline (Bdq) and the mutations of drug resistance-related genes, and to analyze the correlation between drug resistance gene mutation types and drug resistance phenotypes. Methods: From January 2020 to December 2022, 521 strains of MTB identified by Guiyang Public Health Clinical Center were collected, including 253 drug-susceptible tuberculosis (DS-TB) strains and 268 multi-drug resistant tuberculosis (MDR-TB) strains. The conventional drug sensitivity of Mycobacterium tuberculosis and the minimum inhibitory concentration (MIC) of Bdq were detected by microplate method. At the same time, Sanger sequencing was used to identify the mutations of Bdq resistance-related genes Rv0678, atpE and pepQ in all strains, and the whole genome sequencing of Bdq-resistant strains was performed to analyze their drug resistance and molecular mutation characteristics. Results: The Bdq MIC of 521 clinical strains was mainly concentrated in the range of 0.016-0.12 mg/L. Bdq-resistant strains were only detected in MDR strains, with a drug resistance rate of 4.1% (11/268). Known Bdq resistance gene mutations were detected in 11 Bdq phenotype resistant strains, of which 10 were Rv0678 gene mutations, 1 was Rv0678 and pepQ gene mutations, and no atpE gene mutation was detected. There were 8 types of mutations in the Rv0678 gene, including C151T (3/11), 19delG (2/11), G404A (1/11), T284C (1/11), C305T (1/11), G149A (1/11), T95C (1/11) and 201delG (1/11). Our survey found that only one of the 11 patients with Bdq resistance had a history of Bdq medication; moreover, the whole genome sequence analysis of Bdq-resistant strains found that 3 strains were clustered strains, suggesting that transmission is an important cause of Bdq resistance. Conclusions: Bdq had a strong antibacterial activity in the Guizhou region. Mutations in the Rv0678 gene served as the primary determinant of Bdq resistance; and transmission played a significant role in the dissemination of Bdq-resistant strains. The findings highlight the need for Bdq resistance-associated genetic screening and transmission chain surveillance in the control of multidrug-resistant tuberculosis.

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