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Performance of the Genotype MTBDR Line Probe Assay for Detection of Resistance to Rifampin and Isoniazid in Strains of Mycobacterium tuberculosis with Low- and High-Level Resistance

机译:基因型MTBDR线探针测定法在具有低水平和高水平抗性的结核分枝杆菌菌株中检​​测对利福平和异烟肼的抗性的性能

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摘要

We assessed the performance of the Genotype MTBDR line probe assay that offers the simultaneous identification of Mycobacterium tuberculosis and its resistance to rifampin (RIF) and isoniazid (INH) by detecting the most commonly found mutations in the rpoB and katG genes. One hundred thirteen M. tuberculosis isolates were tested. The nucleotide sequences of the katG and inhA genes and the mabA-inhA promoter region were also determined. The MTBDR assay detected 100% and 67% (n = 64) of the strains resistant to RIF and INH, respectively. Among the latter, 62 strains carried a Ser315Thr mutation in katG, 59 of them displaying a high level of resistance to INH. Two strains with a low level of INH resistance had a Ser315Asn mutation. No mutation was found by the MTBDR assay for 31 INH-resistant strains (33%), of which 24 showed a low level of resistance. By DNA sequencing, we found among them various mutations in the KatG protein for 7 strains, a C→T mutation in position −15 of the mabA-inhA promoter in 17 strains, and a Ser94Ala mutation in InhA for 7 strains. In conclusion, the MTBDR assay, which fits easily in the workflow of a routine laboratory, enabled the detection of 100% of the RIF-resistant strains and 89% of the INH-resistant strains with a high level of resistance but only 17% of the strains characterized by a low level of INH resistance, indicating that the test can be used as a rapid method to detect in the same experiment the rifampin-resistant and the high-level isoniazid-resistant strains of M. tuberculosis.
机译:我们评估了基因型MTBDR线探针检测的性能,该检测可通过检测rpoB和katG基因中最常见的突变,从而同时鉴定结核分枝杆菌及其对利福平(RIF)和异烟肼(INH)的抗性。测试了113株结核分枝杆菌。还确定了katG和inhA基因以及mabA-inhA启动子区域的核苷酸序列。 MTBDR分析分别检测到100%和67%(n = 64)的RIF和INH耐药菌株。在后者中,有62株在katG中带有Ser315Thr突变,其中59株表现出对INH的高水平抗性。两种具有低INH抗性的菌株均具有Ser315Asn突变。 MTBDR分析未发现31种INH耐药菌株的突变(33%),其中24株耐药水平较低。通过DNA测序,我们发现其中有7种菌株的KatG蛋白存在各种突变,其中17种菌株的mabA-inhA启动子的-15位C→T突变,以及7种菌株的InhA的Ser94Ala突变。总之,MTBDR分析很容易适应常规实验室的工作流程,能够检测出100%的RIF耐药菌株和89%的INH耐药菌株,但耐药水平很高,但只有17%以低水平的INH耐药性为特征的菌株,表明该试验可作为一种快速方法在同一实验中检测结核分枝杆菌的耐利福平和耐异烟肼的高水平菌株。

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