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Evaluation of a Semi-Automated Reporter Phage Assay for Susceptibility Testing of Mycobacterium tuberculosis Isolates in South Africa

机译:南非结核分枝杆菌药敏试验的半自动记者噬菌体检测方法的评估

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摘要

In a prospective study conducted by laboratory technologists in a diagnostic laboratory in Cape Town, South Africa, a semi-automated phage-based antibiotic susceptibility assay was implemented and the performance of the luciferase reporter mycobacteriophage (LRP) system for susceptibility testing of clinical Mycobacterium tuberculosis complex (MTC) isolates against rifampin and isoniazid was evaluated. Two hundred consecutive clinical MGIT cultures of MTC species were included in this study. Antibiotic susceptibility assays were setup manually for the LRP and BACTEC radiometric systems and read in a plate luminometer and the BACTEC 460 instrument, respectively. Discrepant susceptibility results were resolved by the conventional agar proportion method. Of the 200 secondary cultures prepared for this study, 9 (4.5%) were lost to contamination (LRP 4, BACTEC 1, both 4). All of the remaining 191 cultures underwent susceptibility testing by both methods and the overall agreement between the LRP and BACTEC was 98.4% (rifampin 100%; isoniazid 96.9%). Of the 6 discrepant cultures tested by the agar proportion method, 2 gave results in agreement with the LRP. The sensitivity of the LRP for detection of drug-resistant isolates was 100% for both rifampin (n=9) and isoniazid (n=12). The median turnaround time for susceptibility testing was 2 days with the LRP and 9 days with BACTEC. In conclusion, the semi-automated LRP-based assay offers a rapid and practical approach for accurate susceptibility testing of Mycobacterium tuberculosis cultures in diagnostic laboratories with limited financial resources but with competent technologists.
机译:由实验室技术人员在南非开普敦的诊断实验室中进行的一项前瞻性研究中,实施了基于噬菌体的半自动化抗生素敏感性测定,并且荧光素酶记者分枝杆菌噬菌体(LRP)系统的性能可用于临床结核分枝杆菌的敏感性测试对利福平和异烟肼的复合物(MTC)分离物进行了评估。这项研究包括200个连续的MTC物种的临床MGIT培养。手动对LRP和BACTEC辐射测定系统进行抗生素敏感性测定,并分别在平板发光仪和BACTEC 460仪器中读取。通过常规琼脂比例法解决了不同的药敏结果。在为该研究准备的200种继代培养物中,有9种(4.5%)因污染而丢失(LRP 4,BACTEC 1和4)。其余191种培养物均通过两种方法进行了药敏测试,LRP和BACTEC之间的总体一致性为98.4%(利福平100%;异烟肼96.9%)。通过琼脂比例法测试的6种差异培养物中,有2种的结果与LRP一致。对于利福平(n = 9)和异烟肼(n = 12),LRP检测耐药菌株的敏感性均为100%。药敏试验的中位数周转时间是LRP为2天,BACTEC为9天。总而言之,基于LRP的半自动化分析为诊断实验室中的结核分枝杆菌培养物的准确药敏性测试提供了一种快速而实用的方法,该实验室的财务资源有限,但具有胜任的技术人员。

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