首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Comparison of two commercial assays for the characterization of rpoB mutations in Mycobacterium tuberculosis and description of new mutations conferring weak resistance to rifampicin.
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Comparison of two commercial assays for the characterization of rpoB mutations in Mycobacterium tuberculosis and description of new mutations conferring weak resistance to rifampicin.

机译:两种用于鉴定结核分枝杆菌中rpoB突变的商业检测方法的比较,以及对赋予利福平抗性弱的新突变的描述。

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OBJECTIVES: The aim of this study was to compare the efficiency of two commercial assays, INNO-LiPA Rif.TB and MTBDRplus, for the identification of mutations in the rpoB hot-spot region and to assess the efficiency of these mutations in conferring resistance to rifampicin. METHODS: A collection of 126 rifampicin-resistant Mycobacterium tuberculosis and Mycobacterium africanum isolates and 18 rifampicin-susceptible isolates from different countries were analysed using the two hybridization assays. RESULTS: For 60 strains the hot-spot region of the rpoB gene was sequenced, confirming the results of the hybridization assays and allowing the identification of new mutations. In total, 17 mutations involving 10 codons were observed, two of which are newly described (D516Y and E562G/P564L). Mutations L533P, H526L, D516Y and L511P and the double mutation E562G/P564L conferred a low level of resistance. CONCLUSIONS: The assays INNO-LiPA Rif.TB and MTBDRplus identified rpoB mutations in 98.4% of cases. MTBDRplus provided additional information due to the overlapping hybridization probes and in addition allowed the investigation of katG mutations for isoniazid resistance.
机译:目的:本研究的目的是比较两种商业测定法INNO-LiPA Rif.TB和MTBDRplus的效率,以鉴定rpoB热点区域中的突变,并评估这些突变在赋予抗药性方面的效率。利福平。方法:使用两种杂交方法分析了来自不同国家的126株耐利福平结核分枝杆菌和非洲分枝杆菌,以及18株易感利福平的菌株。结果:对60株rpoB基因的热点区域进行了测序,证实了杂交测定的结果并允许鉴定新的突变。总共观察到17个涉及10个密码子的突变,其中两个是新描述的(D516Y和E562G / P564L)。突变L533P,H526L,D516Y和L511P以及双重突变E562G / P564L赋予了较低的抗性水平。结论:INNO-LiPA Rif.TB和MTBDRplus检测在98.4%的病例中鉴定出rpoB突变。由于杂交探针重叠,MTBDRplus提供了更多信息,此外还允许调查katG突变的异烟肼抗性。

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