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Impact of Fgd1 and ddn diversity in Mycobacterium tuberculosis complex on in vitro susceptibility to PA-824.

机译:结核分枝杆菌复合物中Fgd1和ddn多样性对PA-824体外敏感性的影响。

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摘要

PA-824 is a promising drug candidate for the treatment of tuberculosis (TB). It is in phase II clinical trials as part of the first newly designed regimen containing multiple novel antituberculosis drugs (PA-824 in combination with moxifloxacin and pyrazinamide). However, given that the genes involved in resistance against PA-824 are not fully conserved in the Mycobacterium tuberculosis complex (MTBC), this regimen might not be equally effective against different MTBC genotypes. To investigate this question, we sequenced two PA-824 resistance genes (fgd1 [Rv0407] and ddn [Rv3547]) in 65 MTBC strains representing major phylogenetic lineages. The MICs of representative strains were determined using the modified proportion method in the Bactec MGIT 960 system. Our analysis revealed single-nucleotide polymorphisms in both genes that were specific either for several genotypes or for individual strains, yet none of these mutations significantly affected the PA-824 MICs (
机译:PA-824是用于治疗结核病(TB)的有希望的候选药物。作为第一个新设计方案的一部分,该方案处于II期临床试验中,该方案包含多种新型抗结核药(PA-824与莫西沙星和吡嗪酰胺联合使用)。但是,考虑到与PA-824抗药性有关的基因在结核分枝杆菌复合物(MTBC)中并未完全保守,因此该方案可能对不同的MTBC基因型同样无效。为了研究这个问题,我们在代表主要系统进化谱系的65株MTBC菌株中对两个PA-824抗性基因(fgd1 [Rv0407]和ddn [Rv3547])进行了测序。使用改良比例法在Bactec MGIT 960系统中确定代表性菌株的MIC。我们的分析揭示了两个基因的单核苷酸多态性,这些基因对几种基因型或个别菌株具有特异性,但这些突变均未显着影响PA-824 MIC(

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