Rapid Detection of Ethambutol-Resistant Mycobacterium tuberculosis from Sputum by High-Resolution Melting Analysis in Beijing, China

被引:2
|
作者
Wang, Jun [1 ]
Zhao, Weijie [2 ]
Liu, Rongmei [1 ]
Huo, Fengmin [3 ]
Dong, Lingling [3 ]
Xue, Yi [3 ]
Wang, Yufeng [4 ]
Xue, Zhongtan [4 ]
Ma, Liping [1 ]
Pang, Yu [3 ]
机构
[1] Capital Med Univ, Beijing Chest Hosp, Dept TB, Beijing TB & Thorac Tumor Res Inst, 9 Beiguan St, Beijing 101149, Peoples R China
[2] Capital Med Univ, Beijing Chest Hosp, Clin Trial Agcy Off, Beijing TB & Thorac Tumor Res Inst, Beijing 101149, Peoples R China
[3] Capital Med Univ, Beijing Chest Hosp, Natl Clin Lab TB, Beijing TB & Thorac Tumor Res Inst, 9 Beiguan St, Beijing 101149, Peoples R China
[4] Innovat Alliance TB Diag & Treatment Beijing, Dept Lab Qual Control, Beijing 101149, Peoples R China
来源
关键词
tuberculosis; ethambutol; molecular diagnostic; embB; China; MOLECULAR CHARACTERISTICS; MULTICENTER EVALUATION; NATIONAL-SURVEY; EMBB MUTATIONS;
D O I
10.2147/IDR.S270542
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objective: We conducted a retrospective study to evaluate the performance of MeltPro assay for detecting ethambutol (EMB) susceptibility of Mycobacterium tuberculosis (MTB) isolates in sputum specimens in Beijing, China. Methods: Smear-positive TB patients undergoing MeltPro assay in the Beijing Chest Hospital between January 2019 and December 2019 were included. Phenotypic drug susceptibility testing (DST) was used as the reference standard to calculate the diagnostic accuracy of MeltPro assay for EMB resistance. Sanger sequencing of embB gene was conducted to resolve the discrepancies between MeltPro assay and phenotypic DST. Results: A total of 222 smear-positive patients were included in our analysis. The overall agreement rate between the two assays was 91.4%, with a kappa value of 0.78. Among 59 EMB-resistant TB cases diagnosed by DST, 49 were identified by MeltPro assay, demonstrating a sensitivity of 83.1%. In addition, 154 out of 163 EMB-susceptible patients diagnosed by DST were correctly detected with MeltPro assay, yielding a specificity of 93.9%. The probe frequency associated with the observed EMB-resistance was as follows: A (45/58), B (7/58), and D (6/58), and no EMB-resistance was associated with probe C. The presence of amino acid substitution was observed among all 9 cases with potentially "false-negative" results, including 7 with Met306Ile, 1 with Met306Val, 1 with Gly406Asp, respectively. Conclusion: MeltPro assay is a promising diagnostic tool for the detection of EMB resistance in China. The specific amino acid substitution in embB gene is the major reason for discrepancies between MeltPro assay and phenotypic DST.
引用
收藏
页码:3707 / 3713
页数:7
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