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本文引用的文献

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Tanshinones: First-in-Class Inhibitors of the Biogenesis of the Type 3 Secretion System Needle of for Antibiotic Therapy.丹参酮:用于抗生素治疗的3型分泌系统针状结构生物合成的一流抑制剂
ACS Cent Sci. 2019 Jul 24;5(7):1278-1288. doi: 10.1021/acscentsci.9b00452. Epub 2019 Jun 26.
2
Tyrosol from marine Fungi, a novel Quorum sensing inhibitor against Chromobacterium violaceum and Pseudomonas aeruginosa.海洋真菌来源的酪醇,一种新型的群体感应抑制剂,可抑制紫色色杆菌和铜绿假单胞菌。
Bioorg Chem. 2019 Oct;91:103140. doi: 10.1016/j.bioorg.2019.103140. Epub 2019 Jul 22.
3
Anti-quorum sensing and anti-biofilm activity of 5-hydroxymethylfurfural against Pseudomonas aeruginosa PAO1: Insights from in vitro, in vivo and in silico studies.5-羟甲基糠醛抗铜绿假单胞菌 PAO1 的群体感应和抗生物膜活性:体外、体内和计算研究的见解。
Microbiol Res. 2019 Sep;226:19-26. doi: 10.1016/j.micres.2019.05.001. Epub 2019 May 7.
4
CFTR-PTEN-dependent mitochondrial metabolic dysfunction promotes airway infection.CFTR-PTEN 依赖性线粒体代谢功能障碍促进气道感染。
Sci Transl Med. 2019 Jul 3;11(499). doi: 10.1126/scitranslmed.aav4634.
5
Killing from the inside: Intracellular role of T3SS in the fate of Pseudomonas aeruginosa within macrophages revealed by mgtC and oprF mutants.从内部杀死:通过 mgtC 和 oprF 突变体揭示铜绿假单胞菌在巨噬细胞内的命运的 T3SS 细胞内作用。
PLoS Pathog. 2019 Jun 20;15(6):e1007812. doi: 10.1371/journal.ppat.1007812. eCollection 2019 Jun.
6
Differential effects of alkyl gallates on quorum sensing in Pseudomonas aeruginosa.烷基没食子酸盐对铜绿假单胞菌群体感应的差异影响。
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7
Inhibition of biofilm formation, quorum sensing activity and molecular docking study of isolated 3, 5, 7-Trihydroxyflavone from Alstonia scholaris leaf against P.aeruginosa.从裂果金花叶子中分离得到的 3,5,7-三羟基黄酮对铜绿假单胞菌的生物膜形成抑制、群体感应活性及分子对接研究。
Bioorg Chem. 2019 Jun;87:291-301. doi: 10.1016/j.bioorg.2019.03.050. Epub 2019 Mar 18.
8
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Itaconimides as Novel Quorum Sensing Inhibitors of .异戊烯酰胺类作为群体感应抑制剂的新型研究
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10
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Biotechnol Adv. 2019 Jan-Feb;37(1):177-192. doi: 10.1016/j.biotechadv.2018.11.013. Epub 2018 Nov 27.

减毒联合疗法:一种治疗囊性纤维化患者感染的潜在多靶点协同方法。

Virulence attenuating combination therapy: a potential multi-target synergy approach to treat infections in cystic fibrosis patients.

作者信息

Shaw Elana, Wuest William M

机构信息

Department of Chemistry , Emory University , 1515 Dickey Drive , Atlanta , Georgia 30322 , USA . Email:

Emory Antibiotic Resistance Center , Emory University School of Medicine , 201 Dowman Drive , Atlanta , Georgia 30322 , USA.

出版信息

RSC Med Chem. 2020 Feb 19;11(3):358-369. doi: 10.1039/c9md00566h. eCollection 2020 Mar 1.

DOI:10.1039/c9md00566h
PMID:33479641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7580779/
Abstract

The World Health Organization considers the discovery of new treatments for a top priority. Virulence attenuating combination therapy (VACT) is a pragmatic strategy to improve bacterial clearance, repurpose outmoded antibiotics, improve drug efficacy at lower doses, and reduce the evolution of resistance. and studies have shown that adding a quorum sensing inhibitor or an extracellular polymeric substance repressor to classical antibiotics synergistically improves antipseudomonal activity. This review highlights why VACT could specifically benefit cystic fibrosis patients harboring chronic infections, outlines the current landscape of synergistic combinations between virulence-targeting small-molecules and anti-pseudomonal drugs, and suggests future directions for VACT research.

摘要

世界卫生组织将发现新的治疗方法视为首要任务。减毒联合疗法(VACT)是一种切实可行的策略,可提高细菌清除率、重新利用过时的抗生素、在较低剂量下提高药物疗效并减少耐药性的产生。并且研究表明,在传统抗生素中添加群体感应抑制剂或细胞外聚合物阻遏物可协同提高抗假单胞菌活性。本综述强调了VACT为何能特别惠及患有慢性感染的囊性纤维化患者,概述了靶向毒力的小分子与抗假单胞菌药物之间协同组合的现状,并提出了VACT研究的未来方向。