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A Novel Bactericidal Drug Effective Against Gram-Positive and Gram-Negative Pathogenic Bacteria: Easy as AB569

机译:一种新的杀菌药物,抗革兰氏阳性和革兰氏阴性病原细菌:易于AB569

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摘要

Global antibiotic resistance, driven by intensive antibiotic exposure/abuse, constitutes a serious challenge to all health care, particularly in an era when new antimicrobial development has slowed to a trickle. Recently, we published work demonstrating the discovery and partial mechanism of action of a novel bactericidal agent that is effective against both gram-positive and gram-negative multidrug-resistant bacteria. This drug, called AB569, consists of acidified nitrite (A-NO2-) and EDTA, of which there is no mechanism of resistance. Using both chemistry-, genetic-, and bioinformatics-based techniques, we first discovered that AB569 was able to generate bactericidal levels of nitric oxide (NO), while the EDTA component stabilizedS-nitrosyl thiols, thereby furthering NO and downstream reactive nitrogen species production. This elegant chemistry triggered a paralytic downregulation of vital genes using RNA-seq involved in the synthesis of DNA, RNA, ATP, and protein in the representative ESKAPE pathogen,Pseudomonas aeruginosa.
机译:通过密集的抗生素暴露/滥用驱动的全球抗生素抗性构成对所有医疗保健的严重挑战,特别是在新的抗微生物发育缓慢到涓涓细流时的时代。最近,我们公布了表明新型杀菌剂的发现和部分机制,这些杀菌剂对革兰氏阳性和革兰氏阴性多药抗性细菌有效。这种称为AB569的药物由酸化的亚硝酸盐(A-NO 2-)和EDTA组成,没有抗性机理。使用化学,遗传和生物信息学的基础技术,首先发现AB569能够产生一氧化氮(NO)的杀菌水平,而EDTA组分稳定 - 亚硝基硫醇,从而进一步没有下游的反应性氮气物质生产。这种优雅的化学在代表Eskape病原体,假单胞菌铜绿假单胞菌中,使用RNA-SEQ涉及参与DNA,RNA,ATP和蛋白质的RNA-SEQ的瘫痪性瘫痪。

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