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酮基和氰基硒酸酯用于克服外排泵、群体感应和生物膜介导的耐药性。

Ketone- and Cyano-Selenoesters to Overcome Efflux Pump, Quorum-Sensing, and Biofilm-Mediated Resistance.

作者信息

Szemerédi Nikoletta, Kincses Annamária, Rehorova Katerina, Hoang Lan, Salardón-Jiménez Noemi, Sevilla-Hernández Clotilde, Viktorová Jitka, Domínguez-Álvarez Enrique, Spengler Gabriella

机构信息

Department of Medical Microbiology and Immunobiology, Faculty of Medicine, University of Szeged, Dóm tér 10, 6720 Szeged, Hungary.

Department of Biochemistry and Microbiology, Faculty of Food and Biochemical Technology, University of Chemistry and Technology Prague, Technická 3, 166 28 Prague 6, Czech Republic.

出版信息

Antibiotics (Basel). 2020 Dec 11;9(12):896. doi: 10.3390/antibiotics9120896.

Abstract

The emergence of drug-resistant pathogens leads to a gradual decline in the efficacy of many antibacterial agents, which poses a serious problem for proper therapy. Multidrug resistance (MDR) mechanisms allow resistant bacteria to have limited uptake of drugs, modification of their target molecules, drug inactivation, or release of the drug into the extracellular space by efflux pumps (EPs). In previous studies, selenoesters have proved to be promising derivatives with a noteworthy antimicrobial activity. On the basis of these results, two series of novel selenoesters were synthesized to achieve more potent antibacterial activity on Gram-positive and Gram-negative bacteria. Fifteen selenoesters (eight ketone-selenoesters and seven cyano-selenoesters) were investigated with regards to their efflux pump-inhibiting, anti-quorum-sensing (QS), and anti-biofilm effects . According to the results of the antibacterial activity, the ketone-selenoesters proved to be more potent antibacterial compounds than the cyano-selenoesters. With regard to efflux pump inhibition, one cyano-selenoester on methicillin-resistant and one ketone-selenoester on Typhimurium were potent inhibitors. The biofilm inhibitory capacity and the ability of the derivatives to disrupt mature biofilms were noteworthy in all the experimental systems applied. Regarding QS inhibition, four ketone-selenoesters and three cyano-selenoesters exerted a noteworthy effect on strains.

摘要

耐药病原体的出现导致许多抗菌药物的疗效逐渐下降,这给恰当治疗带来了严重问题。多重耐药(MDR)机制使耐药菌对药物的摄取受限、靶分子发生修饰、药物失活,或通过外排泵(EPs)将药物释放到细胞外空间。在先前的研究中,硒酯已被证明是具有显著抗菌活性的有前景的衍生物。基于这些结果,合成了两个系列的新型硒酯,以实现对革兰氏阳性菌和革兰氏阴性菌更强的抗菌活性。研究了十五种硒酯(八种酮硒酯和七种氰基硒酯)的外排泵抑制、抗群体感应(QS)和抗生物膜作用。根据抗菌活性结果,酮硒酯被证明是比氰基硒酯更强效的抗菌化合物。在外排泵抑制方面,一种对耐甲氧西林菌有效的氰基硒酯和一种对鼠伤寒菌有效的酮硒酯是强效抑制剂。在所有应用的实验系统中,衍生物的生物膜抑制能力和破坏成熟生物膜的能力都很显著。在QS抑制方面,四种酮硒酯和三种氰基硒酯对菌株产生了显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a53/7763688/2ee67ad12125/antibiotics-09-00896-g001.jpg

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