Division of Clinical Microbiology and Molecular Medicine, Department of Laboratory Medicine, All India Institute of Medical Sciences, New Delhi, India.
Department of Microbiology, All India Institute of Medical Sciences, Bhopal, India.
PLoS One. 2020 Mar 4;15(3):e0229419. doi: 10.1371/journal.pone.0229419. eCollection 2020.
Genotype MTBDRsl Version 1 (V1.0) was recommended as an initial test for rapid detection of pre-extensively drug resistant (pre-XDR) and extensively drug resistant tuberculosis (XDR-TB). However, in recent years a number of novel mutations are identified that confer resistance. Thus, Genotype MTBDRsl V2.0 was endorsed by WHO. Though, Genotype MTBDRsl V2.0 has been rolled out in national TB programme in 2018, there is dearth of data from India on its performance for second line drug susceptibility testing (DST). For this, performance of new version was evaluated on 113 MDR-TB isolates. The results showed that 39 (34.5%) of these isolates were resistant to FQ and 7 (6.2%) were XDR by Genotype MTBDRsl V2.0. Amongst the FQ resistant isolates most prevalent mutation was ΔWT3-D94G (17; 38.6%) and N538D (12; 85.7%). Among the AG/CP and KAN resistant isolates most common mutation in the rrs region was ΔWT1-A1401G (5; 71.4%) and C-14T (2; 28.5%) in eis gene. Second line Bactec MGIT-960 detected 40 (35.4%) isolates as resistant to FQ and 6 (5.3%) as XDR isolates, whereas Genotype MTBDRsl V1.0 also detected 39 (34.5%) as resistant to FQ but missed 2 isolates in correctly identifying as XDR (5; 4.4%). Thus, concordance of second line Bactec MGIT-960 with Genotype MTBDRsl V2.0 was similar (100%) for FQ detection but it has improvised the diagnostic sensitivity for correctly identifying XDR isolates. Nevertheless, the cost of Genotype MTBDRsl V2.0 remains an issue for screening of second line drug (SLDs) resistance from countries with high burden of MDR-TB.
基因型 MTBDRsl 版本 1(V1.0)被推荐作为快速检测预广泛耐药(pre-XDR)和广泛耐药结核病(XDR-TB)的初始检测方法。然而,近年来发现了许多新的突变,这些突变赋予了耐药性。因此,世界卫生组织(WHO)认可了基因型 MTBDRsl V2.0。虽然基因型 MTBDRsl V2.0 已于 2018 年在国家结核病规划中推出,但印度缺乏关于其用于二线药物敏感性测试(DST)的性能数据。为此,对 113 株 MDR-TB 分离株进行了新版本的性能评估。结果表明,这些分离株中有 39 株(34.5%)对 FQ 耐药,7 株(6.2%)对 XDR 耐药,基因型 MTBDRsl V2.0 检测。在 FQ 耐药分离株中,最常见的突变是 ΔWT3-D94G(17;38.6%)和 N538D(12;85.7%)。在 AG/CP 和 KAN 耐药分离株中,rrs 区最常见的突变是 ΔWT1-A1401G(5;71.4%)和 eis 基因中的 C-14T(2;28.5%)。二线 Bactec MGIT-960 检测到 40 株(35.4%)分离株对 FQ 耐药,6 株(5.3%)分离株对 XDR 耐药,而基因型 MTBDRsl V1.0 也检测到 39 株(34.5%)对 FQ 耐药,但在正确鉴定为 XDR 时漏检了 2 株(5;4.4%)。因此,二线 Bactec MGIT-960 与基因型 MTBDRsl V2.0 对 FQ 的检测一致性(100%)相似,但提高了正确鉴定 XDR 分离株的诊断敏感性。然而,基因型 MTBDRsl V2.0 的成本仍然是高耐多药结核病负担国家筛选二线药物(SLDs)耐药性的一个问题。