Alamgir Muhammad, Sajjad Mehwish, Baig Mirza Saifullah, Noori Muhammad Yahya
Muhammad Alamgir, M. Sc. Lab Technician, Ojha Institute of Chest Diseases, Dow University of Health Sciences, Karachi, Pakistan.
Mehwish Sajjad, MBBS, M. Phil. Lecturer, Department of Pathology, Dow International Medical College, Dow University of Health Sciences, Karachi, Pakistan.
Pak J Med Sci. 2021 Jul-Aug;37(4):1151-1154. doi: 10.12669/pjms.37.4.3875.
To assess the mutational frequencies in Mycobacterial gene using GeneXpert/MTB Rif Assay in rifampicin resistant patients during 2013-2017 at a tertiary care setting in Urban Sindh, Pakistan.
This Retrospective Descriptive Cross-Sectional Study was conducted at the TB laboratories, Ojha Institute of Chest Diseases, Dow University of Health Sciences. The record of 713 positive cases of Rifampicin Resistant Tuberculosis from January 2013 to December 2017 were analysed. These were diagnosed using GeneXpert® that detects mutations in the 81 base pair region of gene with the help of five molecular probes A, B, C, D and E. All invalid and extra pulmonary samples were excluded.
In total, 713 cases were found to be rifampicin resistant during the five-year period, among which 374 (52.45%) were males while 339 (47.55%) were females. Among the five standard probes A, B, C, D and E, 97.48% of the cases had a single mutation. Among these, mutations in Probe E (66.48%) were the most common, followed by Probe B (14.3%) and Probe D (11.08%). Only 13 cases (1.82%) of double mutations and five cases (0.7%) of triple mutations were detected.
The Probe E region 529-533 appears the most potent site for a mutation and development of rifampicin resistance in the gene in , that encodes the β-subunit of RNA polymerase. The most affected age-group in both males and females is 19-45 Years.
在2013 - 2017年期间,于巴基斯坦信德省城市的一家三级医疗机构中,使用GeneXpert/MTB Rif检测法评估耐利福平患者分枝杆菌基因的突变频率。
这项回顾性描述性横断面研究在道健康科学大学奥贾胸科疾病研究所的结核病实验室进行。分析了2013年1月至2017年12月期间713例耐利福平结核病阳性病例的记录。这些病例使用GeneXpert®进行诊断,该检测法借助五个分子探针A、B、C、D和E检测基因81个碱基对区域的突变。所有无效和肺外样本均被排除。
在这五年期间,共发现713例耐利福平病例,其中374例(52.45%)为男性,339例(47.55%)为女性。在五个标准探针A、B、C、D和E中,97.48%的病例有单个突变。其中,探针E的突变(66.48%)最为常见,其次是探针B(14.3%)和探针D(11.08%)。仅检测到13例(1.82%)双突变和5例(0.7%)三突变。
在编码RNA聚合酶β亚基的基因中,探针E区域529 - 533似乎是该基因发生突变和产生利福平耐药性的最有效位点。男性和女性中受影响最大的年龄组为19 - 45岁。