Genetic Characterization Conferred Co-Resistance to Isoniazid and Ethionamide in Mycobacterium tuberculosis Isolates from Southern Xinjiang, China

被引:3
作者
Cao, Bin [1 ,2 ]
Mijiti, Xiaokaiti [3 ]
Deng, Le-Le [2 ,4 ]
Wang, Quan [3 ]
Yu, Jin-Jie [1 ,2 ]
Anwaierjiang, Aiketaguli [5 ]
Qian, Chengyu [2 ,6 ]
Li, Machao [2 ]
Fang, Dan-Ang [2 ,6 ]
Jiang, Yi [2 ]
Zhao, Li-Li [2 ]
Zhao, Xiuqin [2 ]
Wan, Kanglin [2 ]
Liu, Haican [2 ]
Li, Guilian [2 ]
Yuan, Xiuqin [1 ]
机构
[1] Univ South China, Sch Publ Hlth, Hengyang 421001, Peoples R China
[2] Chinese Ctr Dis Control & Prevent, Natl Inst Communicable Dis Control & Prevent, Collaborat Innovat Ctr Diag & Treatment Infect Dis, State Key Lab Infect Dis Prevent & Control, Beijing 102206, Peoples R China
[3] Xinjiang Med Univ, Affiliated Hosp 8, Urumqi 830000, Peoples R China
[4] Chinese Ctr Dis Control & Prevent, Natl Inst Viral Dis Control & Prevent, Beijing, Peoples R China
[5] Coll Xinjiang Uyghur Med, Hetian 848000, Peoples R China
[6] Wenzhou Med Univ, Sch Lab Med & Life Sci, Wenzhou Key Lab Sanit Microbiol, Key Lab Lab Med,Minist Educ, Wenzhou 325035, Zhejiang, Peoples R China
来源
INFECTION AND DRUG RESISTANCE | 2023年 / 16卷
关键词
cross-resistance; ethionamide; isoniazid; mutation; Mycobacterium tuberculosis; HIGH-LEVEL RESISTANCE; CATALASE-PEROXIDASE; DRUG ETHIONAMIDE; KATG; MUTATIONS; INHA; TRANSMISSION; RIFAMPIN; PREVALENCE; ACTIVATION;
D O I
10.2147/IDR.S407525
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Ethionamide (ETH), a structural analogue of isoniazid (INH), is used for treating multidrug-resistant tuberculosis (MDR-TB). Due to the common target InhA, INH and ETH showed cross-resistance in M. tuberculosis. This study aimed to explore the INH and ETH resistant profiles and genetic mutations conferring independent INH-or ETH-resistance and INH-ETH cross-resistance in M. tuberculosis circulating in south of Xinjiang, China. Methods: From Sep 2017 to Dec 2018, 312 isolates were included using drug susceptibility testing (DST), spoligotyping, and whole genome sequencing (WGS) to analyze the resistance characteristics for INH and/or ETH. Results: Among the 312 isolates, 185 (58.3%) and 127 (40.7%) belonged to the Beijing family and non-Beijing family, respectively; 90 (28.9%) were INH-resistant (INHR) with mutation rates of 74.4% in katG, 13.3% in inhA and its promoter, 11.1% in ahpC and its upstream region, 2.2% in ndh, 0.0% in mshA, whilst 34 (10.9%) were ETH-resistant (ETHR) with mutation rates of 38.2% in ethA, 26.2% in inhA and its promoter, and 5.9% in ndh, 0.0% in ethR or mshA; and 25 (8.0%) were INH-ETH co-resistant (INHRETHR) with mutation rates of 40.0% in inhA and its promoter, and 8% in ndh. katG mutants tended to display high-level resistant to INH; and more inhA and its promoter mutants showed low-level of INH and ETH resistance. The optimal gene combinations by WGS for the prediction of INHR, ETHR, and INHRETHR were, respectively, katG+inhA and its promoter (sensitivity: 81.11%, specificity: 90.54%), ethA+inhA and its promoter+ndh (sensitivity: 61.76%, specificity: 76.62%), and inhA and its promoter+ndh (sensitivity: 48.00%, specificity: 97.65%). Conclusion: This study revealed the high diversity of genetic mutations conferring INH and/or ETH resistance among M. tuberculosis isolates, which would facilitate the study on INHR and/or ETHR mechanisms and provide clues for choosing ETH for MDR treatment and molecular DST methods in south of Xinjiang, China.
引用
收藏
页码:3117 / 3135
页数:19
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