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首页> 外文期刊>Acta microbiologica et immunologica Hungarica: A quarterly of the Hungarian Academy of Sciences >High level association of mutation in KatG315 with MDR and XDR clinical isolates of Mycobacterium tuberculosis in Belarus.
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High level association of mutation in KatG315 with MDR and XDR clinical isolates of Mycobacterium tuberculosis in Belarus.

机译:KatG315中的突变与白俄罗斯结核分枝杆菌的MDR和XDR临床分离株高度相关。

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摘要

The mutation in KatG315 is found in the majority of isoniazid resistant strains worldwide, especially in areas with a high incidence of tuberculosis. A total of 138 isoniazid (INH)-resistant strains of Mycobacterium tuberculosis consisting of 108 MDR (multidrug resistant) and 30 XDR (extensively drug resistant) isolated from patients in different regions of Belarus from 2007 to 2008 were screened by a PCR restriction fragment length polymorphism (RFLP) assay and sequencing. As a result, 97.8% prevalence of the KatG315 mutation was detected in all isolates from patients either actually or previously treated with tuberculosis. This mutation was not found in any of 9 INH-susceptible isolates and 2 standard strains of H37Rv and Academia included in the study. All isolates that contained the mutation in KatG315 were classified as MDR and XDR by a culture-based susceptibility testing method. Among the 30 XDR isolates, 15 (50%), 12 (40%), and 3 (10%) were classified into principal genetic groups (PGG) 1, 2, and 3, respectively. It is concluded that INH-resistant MTB were associated with the mutated KatG315 phenotype. The simplicity of the assay, with 100% specificity, permits its implementation in routine practice at clinical microbiology laboratories for first and fast screening of cultures. This method has potential application for rapid diagnosis of INH resistance due to KatG315 mutation.
机译:在全世界大多数异烟肼耐药菌株中都发现了KatG315的突变,尤其是在结核病高发地区。通过PCR限制性片段长度筛选2007年至2008年从白俄罗斯不同地区分离的138例耐异烟肼(INH)的结核分枝杆菌菌株,包括108例MDR(多药耐药)和30例XDR(广泛耐药)。多态性(RFLP)分析和测序。结果,在来自实际或先前接受结核病治疗的患者的所有分离物中,检测到KatG315突变的流行率为97.8%。在研究中包括的9种INH敏感分离株和2株H37Rv和学术界标准菌株中均未发现此突变。通过基于培养物的敏感性测试方法,所有在KatG315中包含突变的分离株都被分类为MDR和XDR。在30个XDR分离株中,分别有15个(50%),12个(40%)和3个(10%)分为主要遗传组(PGG)1、2和3。结论是耐INH的MTB与突变的KatG315表型有关。该检测方法具有100%的特异性,操作简单,可在临床微生物实验室的常规操作中进行培养的首次和快速筛选。该方法在快速诊断由于KatG315突变引起的INH耐药性方面具有潜在的应用前景。

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