Characterization of isoniazid resistance and genetic mutations in isoniazid-resistant and rifampicin-susceptible Mycobacterium tuberculosis in China

Dongxin Liu , Bing Zhao , Yang Zheng , Xichao Ou , Shengfen Wang , Yang Zhou , Yuanyuan Song , Hui Xia , Qiang Wei , YanLin Zhao
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Abstract

Background

Patients with tuberculosis resistant to isoniazid but susceptible to rifampicin (Hr-Rs TB) remain a neglected demographic, despite a high disease burden and poor outcomes of these patients. The aim of this study was to investigate the characteristics of isoniazid-resistance-related mutations in Mycobacterium tuberculosis and resistance rates to drugs included in WHO-recommended regimens for Hr-Rs patients.

Methods

Mycobacterium tuberculosis isolates (n = 4922) obtained from national tuberculosis drug-resistance surveillance were subjected to whole-genome sequencing to identify Hr-Rs strains. The minimal inhibitory concentrations (MICs) were established for the Hr-Rs strains to determine the isoniazid resistance levels. We also identified drug-resistance-associated mutations for five drugs (fluoroquinolones, ethambutol, pyrazinamide, streptomycin, and amikacin) in the Hr-Rs strains.

Results

Of the 4922 strains, 384 (7.8 %) were Hr-Rs. The subculture of seven strains failed, so 377 (98.2 %) strains underwent phenotypic MIC testing. Among the 384 genotypic Hr-Rs strains, 242 (63.0 %) contained the katG Ser315Thr substitution; 115 (29.9 %) contained the -15C>T in the promoter region of the fabG1 gene; and 16 (4.2 %) contained Ser315Asn in the katG gene. Of the 239 strains with the Ser315Thr substitution, 229 (95.8 %) had MIC ≥ 2 µg/mL, and of the 114 strains with the -15C>T mutation, 103 (90.4 %) had 0.25 µg/mL ≤ MIC ≤ 1 µg/mL. The genotypic resistance rates were 0.8 % (3/384) for pyrazinamide, 2.3 % (9/384) for ethambutol and fluoroquinolones; 39.6 % (152/384) of the strains were resistant to streptomycin, but only 0.5 % (2/384) of the strains were resistant to amikacin.

Conclusion

Ser315Thr in katG was the predominant mutation conferring the Hr-Rs phenotype, followed by the fabG1 -15C>T mutation. The combination of rifampicin, pyrazinamide, ethambutol, and levofloxacin should be effective in the treatment of patients with Hr-Rs tuberculosis because the resistance rates for these drugs in China are low.

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中国耐异烟肼结核分枝杆菌和易感利福平结核分枝杆菌的异烟肼耐药性和基因突变特征
背景对异烟肼耐药但对利福平易感的结核病(Hr-Rs TB)患者仍然是一个被忽视的人群,尽管这些患者的疾病负担很重,治疗效果很差。本研究旨在调查结核分枝杆菌中与异烟肼耐药性相关的突变特征,以及对世界卫生组织推荐的Hr-Rs患者治疗方案中所含药物的耐药率。方法对从全国结核病耐药性监测中获得的结核分枝杆菌分离株(n = 4922)进行全基因组测序,以确定Hr-Rs菌株。我们确定了 Hr-Rs 菌株的最小抑菌浓度 (MIC),以确定其对异烟肼的耐药性水平。我们还在 Hr-Rs 菌株中发现了五种药物(氟喹诺酮类、乙胺丁醇、吡嗪酰胺、链霉素和阿米卡星)的耐药性相关突变。7 株菌株的亚培养失败,因此对 377 株(98.2%)菌株进行了表型 MIC 检测。在 384 株基因型 Hr-Rs 菌株中,242 株(63.0%)含有 katG Ser315Thr 替换;115 株(29.9%)在 fabG1 基因启动子区域含有 -15C>T;16 株(4.2%)在 katG 基因中含有 Ser315Asn。在239株含有Ser315Thr替换的菌株中,229株(95.8%)的MIC≥2 µg/mL,而在114株含有-15C>T突变的菌株中,103株(90.4%)的MIC为0.25 µg/mL ≤ 1 µg/mL。基因型耐药率为:吡嗪酰胺 0.8 %(3/384),乙胺丁醇和氟喹诺酮 2.3 %(9/384);39.6 %(152/384)的菌株对链霉素耐药,但只有 0.结论 katG中的Ser315Thr是产生Hr-Rs表型的主要突变,其次是fabG1 -15C>T突变。由于利福平、吡嗪酰胺、乙胺丁醇和左氧氟沙星这四种药物在中国的耐药率较低,因此这四种药物的联合应用应能有效治疗Hr-Rs肺结核患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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