[A New Method for Determination of Rifampicin and Isoniazid Resistance in Mycobacterium tuberculosis complex Isolates: Capillary Tube Method].

IF 1.1 4区 医学 Q4 MICROBIOLOGY
Nazlı Arslan, Ebru Demiray Gürbüz, Ayşe Aydan Özkütük, Nuran Esen
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引用次数: 0

Abstract

Tuberculosis continues to be an important public health problem worldwide. Culture methods are still considered the gold standard in the diagnosis of tuberculosis and the determination of drug resistance. The most important limitation of these methods is their long turnaround time. Commercial culture systems developed to shorten the duration are emerging as an economic problem, especially for developing countries. Therefore, cheap, fast, easy to apply and objectively evaluable tests are needed. In this study, in addition to culture-based methods for determining RIF and INH resistance in Mycobacterium tuberculosis complex isolates, it was aimed to develop the capillary tube method to accelerate the evaluation process. The study included 27 RIF-resistant, 36 RIF -sensitive, 30 INH-resistant, and 33 INH-sensitive isolates obtained from the mycobacteriology laboratory culture collection, for which susceptibility testing to firstline drugs were previously performed using the BACTEC MGIT 960 system (BD, USA) and were stored. H37Rv standard strain and an external quality control strain (IDT3) with known RIF and INH resistance were used as quality control isolates in the study. As a new testing method, the capillary tube method for detecting rifampicin and isoniazid resistance was compared to the standard BACTEC MGIT 960 system. In the determination of RIF and INH resistance, the sensitivity of the capillary tube method compared to the reference method was determined as 85% and 80%, respectively; however, the specificity values (25% and 45.5%, respectively) for both drugs were found to be low in the studies. The time to detect resistance with the capillary tube method varied between 4-9 days. Capillary tube method, which was developed especially for the rapid identification and treatment of multidrug-resistant isolates, is promising in that it detects resistant strains in a short time with a relatively high sensitivity, although its specificity is very low. It is thought that it would be beneficial to continue the study with a larger number of samples and even improve the method with studies conducted directly from clinical samples.

[一种测定结核分枝杆菌复合菌株对利福平和异烟肼耐药性的新方法:毛细管法]。
结核病仍然是全球重要的公共卫生问题。培养方法仍被认为是诊断结核病和确定耐药性的黄金标准。这些方法最重要的局限是周转时间长。为缩短周转时间而开发的商业培养系统正在成为一个经济问题,尤其是对发展中国家而言。因此,需要廉价、快速、易于应用且可客观评价的检测方法。在本研究中,除了用培养法测定复合结核分枝杆菌对 RIF 和 INH 的耐药性外,还旨在开发毛细管法,以加快评估过程。研究对象包括从结核分枝杆菌实验室培养物收集中获得的 27 株 RIF 耐药株、36 株 RIF 敏感株、30 株 INH 耐药株和 33 株 INH 敏感株分离物,这些分离物之前已使用 BACTEC MGIT 960 系统(美国 BD 公司)进行了一线药物药敏试验,并已保存。H37Rv 标准菌株和已知对 RIF 和 INH 耐药的外部质量控制菌株(IDT3)被用作本研究的质量控制分离株。作为一种新的检测方法,检测利福平和异烟肼耐药性的毛细管法与标准的 BACTEC MGIT 960 系统进行了比较。在检测利福平和异烟肼耐药性时,毛细管法与参照法相比,灵敏度分别为 85% 和 80%;但研究发现,这两种药物的特异性值(分别为 25% 和 45.5%)较低。毛细管法检测耐药性的时间为 4-9 天不等。毛细管法是专门为快速鉴定和处理耐多药的分离株而开发的,它能在短时间内检测出耐药菌株,灵敏度相对较高,但特异性很低。我们认为,继续进行更多样本的研究,甚至通过直接从临床样本中进行研究来改进该方法将是有益的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mikrobiyoloji bulteni
Mikrobiyoloji bulteni 生物-微生物学
CiteScore
1.60
自引率
20.00%
发文量
50
审稿时长
6-12 weeks
期刊介绍: Bulletin of Microbiology is the scientific official publication of Ankara Microbiology Society. It is published quarterly in January, April, July and October. The aim of Bulletin of Microbiology is to publish high quality scientific research articles on the subjects of medical and clinical microbiology. In addition, review articles, short communications and reports, case reports, editorials, letters to editor and other training-oriented scientific materials are also accepted. Publishing language is Turkish with a comprehensive English abstract. The editorial policy of the journal is based on independent, unbiased, and double-blinded peer-review. Specialists of medical and/or clinical microbiology, infectious disease and public health, and clinicians and researchers who are training and interesting with those subjects, are the target groups of Bulletin of Microbiology.
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