U1230 Inserm Unit, Biochimie Pharmaceutique, University of Rennes 1, Rennes, France
U1230 Inserm Unit, Biochimie Pharmaceutique, University of Rennes 1, Rennes, France.
Antimicrob Agents Chemother. 2018 Apr 26;62(5). doi: 10.1128/AAC.02503-17. Print 2018 May.
The extensive use of antibiotics has resulted in a situation where multidrug-resistant pathogens have become a severe menace to human health worldwide. A deeper understanding of the principles used by pathogens to adapt to, respond to, and resist antibiotics would pave the road to the discovery of drugs with novel mechanisms. For bacteria, antibiotics represent clinically relevant stresses that induce protective responses. The recent implication of regulatory RNAs (small RNAs [sRNAs]) in antibiotic response and resistance in several bacterial pathogens suggests that they should be considered innovative drug targets. This minireview discusses sRNA-mediated mechanisms exploited by bacterial pathogens to fight against antibiotics. A critical discussion of the newest findings in the field is provided, with emphasis on the implication of sRNAs in major mechanisms leading to antibiotic resistance, including drug uptake, active drug efflux, drug target modifications, biofilms, cell walls, and lipopolysaccharide (LPS) biosynthesis. Of interest is the lack of knowledge about sRNAs implicated in Gram-positive compared to Gram-negative bacterial resistance.
抗生素的广泛使用导致了多药耐药病原体成为全球人类健康的严重威胁。深入了解病原体适应、应对和抵抗抗生素的原理将为发现具有新机制的药物铺平道路。对于细菌来说,抗生素是一种具有临床相关性的应激源,会诱导产生保护反应。最近的研究表明,调控 RNA(小 RNA [sRNA])在几种细菌病原体对抗生素的反应和耐药性中发挥作用,这表明它们应该被视为创新的药物靶点。这篇综述讨论了细菌病原体利用 sRNA 来对抗抗生素的机制。本文对该领域的最新发现进行了批判性讨论,重点讨论了 sRNA 在导致抗生素耐药性的主要机制中的作用,包括药物摄取、主动药物外排、药物靶标修饰、生物膜、细胞壁和脂多糖 (LPS) 生物合成。值得注意的是,与革兰氏阴性细菌耐药性相比,人们对革兰氏阳性细菌中涉及的 sRNA 知之甚少。