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Enhanced Efflux Activity Facilitates Drug Tolerance in Dormant Bacterial Cells

机译:增强的外排活性促进休眠细菌细胞的药物耐受性

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摘要

Natural variations in gene expression provide a mechanism for multiple phenotypes to arise in an isogenic bacterial population. In particular, a subgroup termed persisters show high tolerance to antibiotics. Previously, their formation has been attributed to cell dormancy. Here we demonstrate that bacterial persisters, under beta-lactam antibiotic treatment, show less cytoplasmic drug accumulation as a result of enhanced efflux activity. Consistently, a number of multi-drug efflux genes, particularly the central component TolC, show higher expression in persisters. Time-lapse imaging and mutagenesis studies further establish a positive correlation between tolC expression and bacterial persistence. The key role of efflux systems, among multiple biological pathways involved in persister formation, indicates that persisters implement a positive defense against antibiotics prior to a passive defense via dormancy. Finally, efflux inhibitors and antibiotics together effectively attenuate persister formation, suggesting a combination strategy to target drug tolerance.
机译:基因表达的自然变化为在同基因细菌种群中出现多种表型提供了一种机制。特别地,一个称为持久性的亚组显示出对抗生素的高度耐受性。以前,它们的形成已归因于细胞休眠。在这里,我们证明了在β-内酰胺类抗生素治疗下,细菌持久性蛋白由于增强的外排活性而显示出较少的细胞质药物积累。一致地,许多多药外排基因,特别是中心成分TolC,在持久性基因中表现出更高的表达。延时成像和诱变研究进一步建立了tolC表达与细菌持久性之间的正相关关系。外排系统在参与持久性形成的多种生物学途径中的关键作用表明,持久性在通过休眠被动防御之前先对抗生素实施了积极防御。最后,外排抑制剂和抗生素一起有效地减轻了持久性物质的形成,提示了针对药物耐受性的联合策略。

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