FluoroCycler XT MTBDR 分析法在肯尼亚临床分离物中检测利福平和异烟肼耐药结核分枝杆菌的诊断准确性。

IF 1.6 Q4 INFECTIOUS DISEASES
International Journal of Mycobacteriology Pub Date : 2024-07-01 Epub Date: 2024-09-14 DOI:10.4103/ijmy.ijmy_202_23
Zakayo Maingi Mwangi, Samson Ireri, Haron Opwaka, Leon Otieno, Joan Simam, Frank Gekara Onyambu, Nellie Mukiri
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引用次数: 0

摘要

背景:耐药性结核病(DR-TB)对公共卫生和治疗构成了重大的全球性挑战。它是一个新出现的全球问题,与发病率和死亡率上升有关,主要出现在中低收入国家。分子技术灵敏度高,能及时准确地提供结核病耐药性检测结果,从而对患者管理计划产生积极影响:研究于 2022 年 1 月至 10 月期间在肯尼亚国家结核病参考实验室(NTRL)进行。共有 243 例结核分枝杆菌(M.tb)临床分离株被纳入研究。根据基因型 MTBDRplus 的结果,这些分离株包括 50 个 rpoB 基因突变的分离株、51 个 katG 基因突变的分离株、51 个 inhA 基因突变的分离株和 91 个没有这些基因突变的结核分枝杆菌分离株。使用 FluoroLyse 提取试剂盒提取分离株的 DNA。使用 FluoroType MTBDR 扩增混合物对 rpoB、InhA 和 katG 基因进行实时聚合酶链反应。对 Genotype MTBDRplus 和 FluoroCycler® MTBDR 检测结果不一致的分离株进行了相应基因的靶向测序,然后使用 Geneious 11.0 版软件对序列进行突变分析:Fluorocycler XT MTBDR 检测法检测 rpoB 基因突变的灵敏度为 86%(95% 置信区间 [CI] 73.0-94.0),检测 katG 基因突变的灵敏度为 96%(95% 置信区间 [CI] 87-100),检测 inhA 基因突变的灵敏度为 92%(95% 置信区间 [CI] 81-98)。该检测方法对 rpoB 的特异性为 97%(95% CI 93-99),对 katG 的特异性为 98%(95% CI 96-100),对 inhA 的特异性为 97%(95% CI 93-99):结论:与基因型 MTBDRplus 相比,FluoroType MTBDR 在检测利福平和异烟肼耐药性突变方面的诊断准确率很高,这表明它适合作为基因型 MTBDRplus 的替代检测方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic Accuracy of FluoroCycler XT MTBDR Assay for Detection of Rifampicin and Isoniazid-resistant Mycobacteria tuberculosis in Clinical Isolates from Kenya.

Background: Drug-resistant tuberculosis (DR-TB) poses a major global challenge to public health and therapeutics. It is an emerging global concern associated with increased morbidity and mortality mostly seen in the low- and middle-income countries. Molecular techniques are highly sensitive and offer timely and accurate results for TB drug resistance testing, thereby positively influencing patient management plan.

Methods: The study was carried out at the National Tuberculosis Reference Laboratory (NTRL) in Kenya in the period between January and October 2022. A total of 243 Mycobacterium tuberculosis (M.tb) clinical isolates were included in the study. These isolates comprised of 50 isolates with mutations in rpoB, 51 isolates with katG mutations, 51 isolates with mutations in inhA, and 91 M.tb isolates lacking mutations in these genes based on Genotype MTBDRplus results. DNA from the isolates was extracted using the FluoroLyse extraction kit. Real-time polymerase chain reaction targeting the rpoB, InhA, and katG genes was performed using the FluoroType MTBDR amplification mix. Isolates with discordant results between Genotype MTBDRplus and FluoroCycler® MTBDR assays underwent targeted sequencing for the respective genes, then, sequences were analyzed for mutations using Geneious version 11.0 software.

Results: The sensitivity of the Fluorocycler XT MTBDR assay for the detection of mutations that confer drug resistance was 86% (95% confidence interval [CI] 73.0-94.0) for rpoB, 96% (95% CI 87-100) for katG and 92% (95% CI 81-98) for inhA. The assay's specificity was 97% (95% CI 93-99) for rpoB, 98% (95% CI 96-100) for katG, and 97% (95% CI 93-99) for inhA.

Conclusion: The diagnostic accuracy of FluoroType MTBDR for the detection of mutations conferring resistance to rifampicin and isoniazid was high compared with that of Genotype MTBDRplus and demonstrates its suitability as a replacement assay for Genotype MTBDRplus.

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来源期刊
CiteScore
2.20
自引率
25.00%
发文量
62
审稿时长
7 weeks
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