The Detection of Mutations and Genotyping of Drug-Resistant Mycobacterium tuberculosis Strains Isolated from Patients in the Rural Eastern Cape Province.

IF 3.4 Q2 INFECTIOUS DISEASES
Lindiwe M Faye, Mojisola C Hosu, Selien Oostvogels, Anzaan Dippenaar, Robin M Warren, Ncomeka Sineke, Sandeep Vasaikar, Teke Apalata
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Abstract

Drug-resistant tuberculosis (DR-TB) is still a major public health concern in South Africa. Mutations in M. tuberculosis can cause varying levels of phenotypic resistance to anti-TB medications. There have been no prior studies on gene mutations and the genotyping of DR-TB in the rural Eastern Cape Province; hence, we aimed to identify DR-TB mutations, genetic diversity, and allocated lineages among patients in this area. Using Xpert® MTB/RIF, we assessed the rifampin resistance of sputum samples collected from 1157 patients suspected of having tuberculosis. GenoType MTBDR plus VER 2.0 was used for the detection of mutations causing resistance to anti-TB medications. The next step was to spoligotype 441 isolates. The most prevalent rifampin resistance-conferring mutations were in rpoB codon S531L in INH-resistant strains; the katG gene at codon S315TB and the inhA gene at codon C-15TB had the most mutations; 54.5% and 24.7%, respectively. In addition, 24.6% of strains showed mutations in both the rpoB and inhA genes, while 69.9% of strains showed mutations in both the katG and rpoB genes. Heteroresistance was seen in 17.9% of all cases in the study. According to spoligotyping analysis, Beijing families predominated. Investigation of the evolutionary lineages of M. tuberculosis isolates can be carried out using the information provided by the study's diversity of mutations. In locations wherein these mutations have been discovered, decision-making regarding the standardization of treatment regimens or individualized treatment may be aided by the detection frequency of rpoB, katG, and inhA mutations in various study areas.

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东开普省农村地区患者结核分枝杆菌耐药菌株突变检测及基因分型分析。
耐药结核病(DR-TB)仍然是南非一个主要的公共卫生问题。结核分枝杆菌的突变可引起对抗结核药物不同程度的表型耐药性。目前尚未对东开普省农村地区耐药结核病的基因突变和基因分型进行研究;因此,我们旨在确定该地区患者的耐药结核病突变、遗传多样性和分配谱系。使用Xpert®MTB/RIF,我们评估了从1157例疑似结核病患者收集的痰样本的利福平耐药性。基因型MTBDR加VER 2.0用于检测引起抗结核药物耐药的突变。下一步是对441株分离物进行spoligo型分析。inh耐药菌株中最常见的利福平耐药突变为rpoB密码子S531L;密码子S315TB处的katG基因和C-15TB处的inhA基因突变最多;分别为54.5%和24.7%。此外,24.6%的菌株rpoB和inhA基因同时突变,69.9%的菌株katG和rpoB基因同时突变。本研究中,17.9%的病例出现异耐药。根据spoligotyping分析,北京家族占主导地位。利用突变多样性研究提供的信息,可以对结核分枝杆菌分离株的进化谱系进行调查。在已发现这些突变的地区,各研究区域rpoB、katG和inhA突变的检测频率可能有助于制定治疗方案的标准化或个体化治疗。
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
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
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