Synergistic action of substituted indole derivatives and clinically used antibiotics against drug-resistant bacteria

被引:6
作者
Turner, Danielle N. [1 ,2 ]
Edwards, Leslie [1 ,2 ]
Kornienko, Alexander [1 ,2 ,3 ]
Frolova, Liliya V. [1 ,2 ]
Rogelj, Snezna [1 ,2 ]
机构
[1] New Mexico Inst Min & Technol, Dept Chem, 801 Leroy Pl, Socorro, NM 87801 USA
[2] New Mexico Inst Min & Technol, Dept Biol, 801 Leroy Pl, Socorro, NM 87801 USA
[3] Texas State Univ, Dept Chem & Biochem, San Marcos, TX 78666 USA
关键词
antibiotics; Gram-positive bacteria; infectious disease therapeutics; MRSA; multidrug resistance; BETA-LACTAM COMBINATIONS; PSEUDOMONAS-AERUGINOSA; ENTEROCOCCUS-FAECALIS; MECHANISMS;
D O I
10.2217/fmb-2019-0094
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Aim: The current report describes the discovery of indole derivatives that synergize with standard antibiotics. Materials & methods: The antibacterial activities were determined using an optimized time-kill method, while viability of mammalian cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Results: The synergy is observed with methicillin- and vancomycin-resistant Staphylococcus aureus bacterial strains, against which the standard antibiotics show no activities of their own. Our indole derivatives in combination with antibiotics lack toxicity toward mammalian cells, do not promote the evolution of resistance of S. aureus in comparison to clinically established antibiotics, and likely work by permeabilizing bacterial cell membranes. Conclusion: The above-mentioned findings demonstrate the potential clinical applications of our indole derivatives. Graphical abstract
引用
收藏
页码:579 / 590
页数:12
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