检测结核分枝杆菌对利福平抗药性临界浓度的比较评估

Chang-Ki Kim, H. Huh, Jeong Su Park, Taesoung Kim, Jae Han Sohn
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引用次数: 0

摘要

背景:利福平在结核病治疗中发挥着重要作用。近年来,分子检测技术的引入使利福平耐药性的快速检测成为可能,这导致了与传统方法的差异。世界卫生组织(WHO)分析了诱发利福平耐药性的 rpoB 基因突变,发现了某些导致边缘耐药性的突变,而这些突变往往无法通过传统检测方法检测出来。因此,世卫组织将 7H10 和 MGIT 960 的利福平耐药性标准浓度从 1.0 μg/mL 下调至 0.5 μg/mL。本研究旨在评估临界浓度的这一变化对检测结核分枝杆菌的边缘利福平耐药性的影响。研究方法对 2021 年 5 月至 2022 年 5 月期间提交抗结核药敏试验的结核菌株进行分析。三家机构参与其中;首尔临床实验室使用琼脂比例法,而三星医疗中心和首尔大学盆唐医院则使用 MGIT 960 系统检测原始浓度和修订浓度。对于出现差异的菌株,通过 rpoB 基因测序确认了突变。结果研究期间共进行了 1,596 次有效的药敏试验。在 1.0 μg/mL 浓度和 0.5 μg/mL 浓度下,分别有 35 个病例(2.19%)和 38 个病例(2.38%)对利福平产生耐药性,而在 158 个病例(9.90%)中发现对异烟肼产生耐药性。在三株利福平差异菌株中,一株存在 H445L 突变,其余两株存在 L452P 突变。这些突变被归类为边缘耐药。结论采用新的利福平临界浓度后,耐药率增加了 0.19%,检出病例增加了 8.57%。此外,尽管使用了大量对利福平敏感的菌株进行检测,但并没有得到错误的耐药性结果。因此,新临界浓度的应用被认为有利于耐利福平结核病的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative evaluation of critical concentrations for detecting borderline rifampin resistance in Mycobacterium tuberculosis
Background: Rifampin plays an important role in tuberculosis treatment. In recent years, the introduction of molecular testing techniques has enabled the rapid detection of rifampin resistance, leading to discrepancies with conventional methods. The World Health Organization (WHO) has analyzed mutations in the rpoB gene that induce rifampin resistance and identified certain mutations causing borderline resistance, which are often undetected using conventional tests. Consequently, the WHO has lowered the rifampin resistance criterion concentration from 1.0 to 0.5 μg/mL in 7H10 and MGIT 960. The present study aimed to evaluate the impact of this change in critical concentration on the detection of borderline rifampin resistance in Mycobacterium tuberculosis. Methods: Tuberculosis strains submitted for antituberculosis drug susceptibility testing from May 2021–2022 were analyzed. Three institutions participated; the Seoul Clinical Laboratories used the agar proportion method, whereas the Samsung Medical Center and Seoul National University Bundang Hospital utilized the MGIT 960 system to test both the original and revised concentrations. Mutations were confirmed through rpoB gene sequencing for strains showing discrepancies. Results: A total of 1,596 valid susceptibility tests were conducted during the study period. Rifampin resistance was detected in 35 cases (2.19%) at 1.0 μg/mL and in 38 cases (2.38%) at 0.5 μg/mL, whereas isoniazid resistance was observed in 158 cases (9.90%). Among the three rifampin discrepancy strains, one harbored an H445L mutation, whereas the remaining two exhibited an L452P mutation. These mutations were classified as borderline resistant. Conclusion: Applying the new rifampin critical concentration resulted in a 0.19% increase in resistance rate and an 8.57% increase in detection cases. Additionally, despite testing with large number of rifampin-susceptible strains, no false resistance results were obtained. Therefore, the application of the new critical concentration is considered beneficial for the management of rifampin-resistant tuberculosis.
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