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色酮衍生物对尿路致病性大肠杆菌的抗菌和抗生物膜活性。

Antimicrobial and antibiofilm activities of chromone derivatives against uropathogenic Escherichia coli.

机构信息

School of Chemical Engineering, Yeungnam University, 280 Daehak-Ro, Gyeongsan 38541, Republic of Korea.

School of Chemical Engineering, Yeungnam University, 280 Daehak-Ro, Gyeongsan 38541, Republic of Korea.

出版信息

Microbiol Res. 2024 Jan;278:127537. doi: 10.1016/j.micres.2023.127537. Epub 2023 Oct 27.

Abstract

Uropathogenic Escherichia coli (UPEC) is a urinary tract pathogen responsible for most nosocomial urinary tract infections and can cause severe conditions like acute cystitis of the bladder or pyelonephritis. UPEC harbors a host of virulence factors like curli, hemolysin, siderophore, and motility factors and can form biofilm-like communities and quiescent reservoirs that aid its survival. This study was performed to investigate the antibiofilm, antimicrobial, and antivirulence potentials of three chromone derivatives, namely, 6-bromo 3-formylchromone, 6-chloro 3-formylchromone, and 3-formyl 6-isopropylchromone. These chromones had MICs against UPEC of 20, 20, and 50 µg/ml, respectively, inhibited biofilm formation by 72-96% at 20 µg/ml, and inhibited UPEC-associated virulence factors, that is, hemolysis, motility, curli, siderophore production, indole production, quiescent colony formation, and cell surface hydrophobicity. Gene expression analysis indicated these three derivatives downregulated virulence genes associated with toxins, biofilm production, and stress regulation and suggested they might target two-component UvrY response regulator. 3D-QSAR analysis showed that substitutions at the third and sixth positions of the chromone scaffold favor antimicrobial activity against UPEC. Furthermore, ADME profiles and C. elegans cytotoxicity assays indicated that these chromone derivatives are potent, safe drug candidates.

摘要

尿路致病性大肠杆菌(UPEC)是一种引起大多数医院获得性尿路感染的病原体,可引起严重疾病,如膀胱急性膀胱炎或肾盂肾炎。UPEC 携带多种毒力因子,如卷曲、溶血素、铁载体和运动因子,并能形成类似生物膜的群落和休眠库,帮助其生存。本研究旨在研究三种色酮衍生物,即 6-溴-3-甲酰基色酮、6-氯-3-甲酰基色酮和 3-甲酰基-6-异丙基色酮的抗生物膜、抗菌和抗毒力潜力。这些色酮对 UPEC 的 MIC 分别为 20、20 和 50μg/ml,在 20μg/ml 时抑制生物膜形成 72-96%,并抑制 UPEC 相关毒力因子,即溶血、运动、卷曲、铁载体产生、吲哚产生、休眠菌落形成和细胞表面疏水性。基因表达分析表明,这三种衍生物下调了与毒素、生物膜产生和应激调节相关的毒力基因,表明它们可能靶向双组分 UvrY 反应调节剂。3D-QSAR 分析表明,色酮骨架的第三和第六位取代有利于对抗 UPEC 的抗菌活性。此外,ADME 概况和秀丽隐杆线虫细胞毒性试验表明,这些色酮衍生物是有效的、安全的候选药物。

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