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本文引用的文献

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Cell-wall recycling and synthesis in Escherichia coli and Pseudomonas aeruginosa - their role in the development of resistance.大肠杆菌和铜绿假单胞菌中的细胞壁循环利用与合成——它们在耐药性发展中的作用
J Med Microbiol. 2018 Jan;67(1):1-21. doi: 10.1099/jmm.0.000636. Epub 2017 Nov 29.
2
Discovery of new RNA classes and global RNA-binding proteins.新RNA类别和全局RNA结合蛋白的发现。
Curr Opin Microbiol. 2017 Oct;39:152-160. doi: 10.1016/j.mib.2017.11.016. Epub 2017 Nov 24.
3
New aspects of RNA-based regulation by Hfq and its partner sRNAs.基于 Hfq 及其伴侣 sRNAs 的 RNA 调控的新方面。
Curr Opin Microbiol. 2018 Apr;42:53-61. doi: 10.1016/j.mib.2017.10.014. Epub 2017 Nov 7.
4
Impact of bacterial sRNAs in stress responses.细菌 sRNAs 在应激反应中的作用。
Biochem Soc Trans. 2017 Dec 15;45(6):1203-1212. doi: 10.1042/BST20160363. Epub 2017 Nov 3.
5
When eukaryotes and prokaryotes look alike: the case of regulatory RNAs.真核生物与原核生物相似时:调控 RNA 案例。
FEMS Microbiol Rev. 2017 Sep 1;41(5):624-639. doi: 10.1093/femsre/fux038.
6
Probing the sRNA regulatory landscape of P. aeruginosa: post-transcriptional control of determinants of pathogenicity and antibiotic susceptibility.探究铜绿假单胞菌的小RNA调控格局:致病性和抗生素敏感性决定因素的转录后调控
Mol Microbiol. 2017 Dec;106(6):919-937. doi: 10.1111/mmi.13857. Epub 2017 Nov 2.
7
Small RNAs in vancomycin-resistant Enterococcus faecium involved in daptomycin response and resistance.万古霉素耐药粪肠球菌中小 RNA 参与达托霉素的反应和耐药性。
Sci Rep. 2017 Sep 11;7(1):11067. doi: 10.1038/s41598-017-11265-2.
8
Lessons from the Environmental Antibiotic Resistome.环境抗生素耐药组的启示
Annu Rev Microbiol. 2017 Sep 8;71:309-329. doi: 10.1146/annurev-micro-090816-093420. Epub 2017 Jun 28.
9
Structural Basis for Ribosome Rescue in Bacteria.细菌中核糖体救援的结构基础。
Trends Biochem Sci. 2017 Aug;42(8):669-680. doi: 10.1016/j.tibs.2017.05.009. Epub 2017 Jun 16.
10
Burden of antimicrobial resistance in an era of decreasing susceptibility.在抗菌药物敏感性降低的时代,抗菌药物耐药性的负担。
Expert Rev Anti Infect Ther. 2017 Jul;15(7):663-676. doi: 10.1080/14787210.2017.1337508. Epub 2017 Jun 13.

细菌通过调控 RNA 对抗生素的适应性。

Bacterial Adaptation to Antibiotics through Regulatory RNAs.

机构信息

U1230 Inserm Unit, Biochimie Pharmaceutique, University of Rennes 1, Rennes, France

U1230 Inserm Unit, Biochimie Pharmaceutique, University of Rennes 1, Rennes, France.

出版信息

Antimicrob Agents Chemother. 2018 Apr 26;62(5). doi: 10.1128/AAC.02503-17. Print 2018 May.

DOI:10.1128/AAC.02503-17
PMID:29530859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5923175/
Abstract

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.

摘要

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。