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首页> 外文期刊>Indian Journal of Medical Microbiology >Mutations at embB306 codon and their association with multidrug resistant M. tuberculosis clinical isolates
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Mutations at embB306 codon and their association with multidrug resistant M. tuberculosis clinical isolates

机译:embB306密码子突变及其与多药耐药结核分枝杆菌临床分离株的关系

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Purpose: The presence of embB306 mutation in ethambutol (EMB)-susceptible (EMBs) clinical isolates questions the significance of these mutations in conferring resistance to EMB. The present study was carried out to determine the occurrence of embB306 mutation in EMB-resistant (EMBr) and EMBs strains of M. tuberculosis. One hundred and four multidrug-resistant tuberculosis (MDR-TB) strains were also included to establish the relevance of excessive use of rifampicin (RIF) and isoniazid (INH) in occurrence of embB306 mutations in EMBs M. tuberculosis isolates. Materials and Methods: Deoxyribonucleic acid (DNA) from M. tuberculosis clinical strains was isolated by cetyltrimethylammonium bromide (CTAB) method. Phenotypic and genotypic drug susceptibility testing (DST) was performed on 354 M. tuberculosis isolates by using standard proportion method and multiplex-allele-specific polymerase chain reaction assay, respectively. Results: The overall frequency of embB306 mutations in EMBr isolates was found to be five times higher than its occurrence in EMB-susceptible isolates (50% vs 10%). Further, the association between embB306 mutation and EMB-resistance was observed to be statistically significant (P = 0.000). Conclusion: The embB306 is not only the main causative mutation of EMB resistance, but is a sensitive applicant marker for EMB-resistance study.
机译:目的:乙胺丁醇(EMB)易感性(EMBs)临床分离物中emBB306突变的存在质疑这些突变在赋予EMB抗性中的重要性。进行本研究以确定在结核分枝杆菌的EMB耐药(EMBr)和EMBs菌株中embB306突变的发生。还包括了104个耐多药结核病(MDR-TB)菌株,以确定在EMBs结核分枝杆菌分离物中发生embB306突变时过量使用利福平(RIF)和异烟肼(INH)的相关性。材料与方法:采用十六烷基三甲基溴化铵(CTAB)法分离结核分枝杆菌临床菌株中的脱氧核糖核酸(DNA)。使用标准比例法和多重等位基因特异性聚合酶链反应法分别对354株结核分枝杆菌进行了表型和基因型药敏试验(DST)。结果:发现EMBr分离株中embB306突变的总频率是其在EMB敏感分离株中发生的频率的五倍(50%比10%)。此外,观察到embB306突变与EMB耐药性之间的关联具有统计学意义(P = 0.000)。结论:embB306不仅是EMB耐药性的主要致病突变,而且是EMB耐药性研究的敏感申请人标记。

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