TB Discovery Research, Infectious Disease Research Institute, Seattle, Washington 98104, United States.
Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, Washington 98109, United States.
ACS Infect Dis. 2023 Oct 13;9(10):1981-1992. doi: 10.1021/acsinfecdis.3c00275. Epub 2023 Sep 14.
New drugs to treat tuberculosis which target intractable bacterial populations are required to develop shorter and more effective treatment regimens. The benzene amide ether scaffold has activity against intracellular , but low activity against extracellular, actively replicating . We determined that these molecules have bactericidal activity against non-replicating but not actively replicating bacteria. Exposure to compounds depleted ATP levels in non-replicating bacteria and increased the oxygen consumption rate; a subset of molecules led to the accumulation of intrabacterial reactive oxygen species. A comprehensive screen of strains identified a number of under-expressing strains as more sensitive to compounds under replicating conditions including QcrA and QcrB hypomorphs. We determined the global gene expression profile after compound treatment for both replicating and nutrient-starved . We saw compound-dependent changes in the expression of genes involved in energy metabolism under both conditions. Taken together, our data suggest that the scaffold targets respiration in .
需要开发新的治疗结核病的药物来靶向难以治疗的细菌群体,以制定更短、更有效的治疗方案。苯甲酰胺醚支架对细胞内的有活性,但对细胞外的、活跃复制的活性低。我们确定这些分子对非复制的有杀菌活性,但对活跃复制的细菌没有活性。暴露于化合物会降低非复制细菌中的 ATP 水平,并增加耗氧量;一组分子导致细胞内活性氧物质的积累。对菌株的全面筛选确定了一些表达水平较低的菌株在复制条件下对化合物更敏感,包括 QcrA 和 QcrB 的拟态。我们确定了化合物处理后复制和营养饥饿状态下的的全基因表达谱。我们在两种条件下都观察到与能量代谢相关的基因表达在化合物依赖性变化。总的来说,我们的数据表明该支架靶标在中的呼吸作用。