Collapsing the Proton Motive Force to Identify Synergistic Combinations against Staphylococcus aureus

被引:189
作者
Farha, Maya A. [1 ,2 ]
Verschoor, Chris P. [3 ]
Bowdish, Dawn [3 ]
Brown, Eric D. [1 ,2 ]
机构
[1] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Michael G DeGroote Inst Infect Dis Res, Hamilton, ON L8N 3Z5, Canada
[3] McMaster Univ, McMaster Immunol Res Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada
来源
CHEMISTRY & BIOLOGY | 2013年 / 20卷 / 09期
基金
加拿大健康研究院;
关键词
ESCHERICHIA-COLI; ANTIBACTERIAL AGENTS; ATP SYNTHESIS; MEMBRANE; BACTERIA; SYSTEMS; PHOSPHORYLATION; DEPOLARIZATION; ANTIBIOTICS; DAPTOMYCIN;
D O I
10.1016/j.chembiol.2013.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pathways of bacterial energy metabolism, such as the proton motive force (PMF), have largely remained unexplored as drug targets, owing to toxicity concerns. Here, we elaborate on a methodical and systematic approach for targeting the PMF using chemical combinations. We began with a high-throughput screen to identify molecules that selectively dissipate either component of the PMF, Delta Psi or Delta pH, in Staphylococcus aureus. We uncovered six perturbants of PMF, three that countered Delta Psi and three that selectively dissipated Delta pH. Combinations of dissipators of Delta Psi with dissipators of Delta pH were highly synergistic against methicillin-resistant S. aureus. Cytotoxicity analyses on mammalian cells revealed that the dose-sparing effect of the observed synergies could significantly reduce toxicity. The discovery and combination of modulators of Delta Psi and Delta pH may represent a promising strategy for combating microbial pathogens.
引用
收藏
页码:1168 / 1178
页数:11
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