Rajendran Priya, Kumar Michel Prem, Thiruvengadam Kannan, Sreenivasan Prabu, Veeraraghavan Thiyagarajan, Ramalingam Radhakrishnan, Hasini Sindhu, Dhanaraju Thangaraj, Kuppamuthu Ramakrishnan, Shanmugam Sivakumar, Frederick Asha, Padmapriyadarsini Chandrasekaran
Department of Bacteriology, ICMR - National Institute for Research in Tuberculosis, India.
Department of Epidemiology, ICMR - National Institute for Research in Tuberculosis, India.
Tuberculosis (Edinb). 2022 Mar;133:102182. doi: 10.1016/j.tube.2022.102182. Epub 2022 Feb 12.
With increasing use of Xpert MTB/RIF a point of care molecular test for simultaneous detection of TB and resistance to rifampicin, a growing number of rifampicin resistant cases are being detected and notified. Insights into the variation and frequencies in the probe mutations obtained through Xpert testing in the RRTB case will form the baseline information for further investigation on drug resistance. In this study we did a retrospective analysis of the GeneXpert data obtained from patient samples received at a National reference laboratory in Chennai between the years 2014 and 2020 to look at the probe distribution, the variation in the mutation and explore its significance. Probe E mutation was most commonly identified followed by Probe D, Probe A, Probe B and Probe C. Coexistence of multiple probe mutations in low bacillary load samples could be related to prolonged amplification cycle leading to delayed hybridization of probes. In such instances reporting false RR in xpert testing is possible. The probe mutations of RR should be monitored in depth with inclusion of codon specific targets for management of drug sensitive TB. In addition, heteroresistance needs to be further tested by alternative genotypic methods to avoid false resistance.
随着用于同时检测结核病和利福平耐药性的即时分子检测Xpert MTB/RIF使用的增加,越来越多的利福平耐药病例被检测和通报。通过Xpert检测在利福平耐药结核病(RRTB)病例中获得的探针突变的变异情况和频率的见解,将为进一步研究耐药性提供基线信息。在本研究中,我们对2014年至2020年间在金奈一家国家参考实验室收到的患者样本中获得的数据进行了回顾性分析,以观察探针分布、突变变异并探讨其意义。最常鉴定出探针E突变,其次是探针D、探针A、探针B和探针C。低菌量样本中多个探针突变的共存可能与扩增周期延长导致探针杂交延迟有关。在这种情况下,Xpert检测中可能会报告假的利福平耐药。应深入监测利福平耐药的探针突变,纳入密码子特异性靶点以管理药物敏感结核病。此外,需要通过替代基因分型方法进一步检测异质性耐药,以避免假耐药。