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Photo‐Disassembly of Membrane Microdomains Revives Conventional Antibiotics against MRSA

机译:膜微滴的光脱摩者对MRSA恢复常规抗生素

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Confronted with the rapid evolution and dissemination of antibiotic resistance, there is an urgent need to develop alternative treatment strategies for drug‐resistant pathogens. Here, an unconventional approach is presented to restore the susceptibility of methicillin‐resistant S. aureus (MRSA) to a broad spectrum of conventional antibiotics via photo‐disassembly of functional membrane microdomains. The photo‐disassembly of microdomains is based on effective photolysis of staphyloxanthin, the golden carotenoid pigment that gives its name. Upon pulsed laser treatment, cell membranes are found severely disorganized and malfunctioned to defense antibiotics, as unveiled by membrane permeabilization, membrane fluidification, and detachment of membrane protein, PBP2a. Consequently, the photolysis approach increases susceptibility and inhibits development of resistance to a broad spectrum of antibiotics including penicillins, quinolones, tetracyclines, aminoglycosides, lipopeptides, and oxazolidinones. The synergistic therapy, without phototoxicity to the host, is effective in combating MRSA both in vitro and in vivo in a mice skin infection model. Collectively, this endogenous chromophore‐targeted phototherapy concept paves a novel platform to revive conventional antibiotics to combat drug‐resistant S. aureus infections as well as to screen new lead compounds.
机译:面对抗生素抗性的快速进化和传播,迫切需要为耐药病原体开发替代治疗策略。这里,提出了一种非常规方法,以通过功能膜微膜的光脱模恢复甲氧西林抗性S.UUREUS(MRSA)的敏感性至广泛的常规抗生素。微泡的光脱臼是基于葡萄干黄素的有效光解,金胡萝卜素颜料赋予其名称。在脉冲激光处理后,发现细胞膜严重紊乱和失常的防御抗生素,被膜透露,膜流量和膜蛋白,PBP2A的脱落所亮相。因此,光解方法增加了易感性并抑制了抗性抗生素的抗性的发展,包括青霉素,喹诺酮,四环素,氨基糖苷,脂肪肽和恶唑烷酮。在没有光毒性对宿主的情况下,协同疗法有效在小鼠皮肤感染模型中对体外和体内混合MRSA。统称,这种内源性发色团靶向光疗概念铺设了一种新颖的平台来恢复常规抗生素来打击耐药性的耐药性S.UUREUS感染以及筛选新的铅化合物。

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