首页> 美国卫生研究院文献>International Journal of Microbiology >The Differential Gene Expression Pattern of Mycobacterium tuberculosis in Response to Capreomycin and PA-824 versus First-Line TB Drugs Reveals Stress- and PE/PPE-Related Drug Targets
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The Differential Gene Expression Pattern of Mycobacterium tuberculosis in Response to Capreomycin and PA-824 versus First-Line TB Drugs Reveals Stress- and PE/PPE-Related Drug Targets

机译:结核分枝杆菌对一线结核病药物和PA-824的差异基因表达模式与一线结核病药物揭示了应激和与PE / PPE相关的药物靶标

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摘要

Tuberculosis is a leading infectious disease causing millions of deaths each year. How to eradicate mycobacterial persistence has become a central research focus for developing next-generation TB drugs. Yet, the knowledge in this area is fundamentally limited and only a few drugs, notably capreomycin and PA-824, have been shown to be active against non-replicating persistent TB bacilli. In this study, we performed a new bioinformatics analysis on microarray-based gene expression data obtained from the public domain to explore genes that were differentially induced by drugs between the group of capreomycin and PA-824 and the group of mainly the first-line TB drugs. Our study has identified 42 genes specifically induced by capreomycin and PA-824. Many of these genes are related to stress responses. In terms of the distribution of identified genes in a specific category relative to the whole genome, only the categories of PE/PPE and conserved hypotheticals have statistical significance. Six among the 42 genes identified in this study are on the list of the top 100 persistence targets selected by the TB Structural Genomics Consortium. Further biological elucidation of their roles in mycobacterial persistence is warranted.
机译:结核病是一种主要的传染病,每年导致数百万人死亡。如何消除分枝杆菌的持久性已成为开发下一代结核病药物的中心研究重点。然而,该领域的知识从根本上来说是有限的,并且仅显示出少数药物,特别是红霉素和PA-824,对非复制型持久性结核杆菌具有活性。在这项研究中,我们对从公共领域获得的基于微阵列的基因表达数据进行了新的生物信息学分析,以探索由霉素和PA-824组与主要一线结核病组之间的药物差异诱导的基因毒品。我们的研究确定了42种由毛霉素和PA-824特异性诱导的基因。这些基因中的许多与应激反应有关。在相对于整个基因组的特定类别中已识别基因的分布方面,只有PE / PPE类别和保守假设具有统计意义。在这项研究中鉴定的42个基因中,有6个在TB结构基因组学联盟选择的前100个持久性目标清单中。需要进一步生物学阐明它们在分枝杆菌持久性中的作用。

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