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高良姜协同恢复万古霉素对耐万古霉素粪肠球菌的抗菌活性。

Galangin synergistically revives the antibacterial activity of vancomycin against vancomycin-resistant Enterococcus faecium.

作者信息

Ayamuang Intu-Orn, Teethaisong Yothin, Sirichaiwetchakoon Kittipot, Suknasang Siriporn, Watthana Santi, Chaiseha Yupaporn, Eumkeb Griangsak

机构信息

School of Biology, Institute of Science, Suranaree University of Technology, University Avenue, Muang District, Nakhon Ratchasima 30000, Thailand.

Department of Medical Sciences, Faculty of Allied Health Sciences, Burapha University, Longhaad Bangsaen Road, Muang District, Chon Buri 20131, Thailand.

出版信息

J Appl Microbiol. 2025 Jan 6;136(1). doi: 10.1093/jambio/lxaf011.

Abstract

AIMS

Enterococcus faecium is one of the most important opportunistic pathogens threatening human health worldwide. Resistance to vancomycin (VAN) is increasing at an alarming rate. Resurrecting antibiotics using a combination approach is a promising alternative avenue. Galangin (GAL) is a bioactive compound constituted in herbal plants. This study aimed to evaluate the synergistic activity of the combination of GAL and VAN and mode of action against vancomycin-resistant E. faecium (VREfm) strains.

METHODS AND RESULTS

The minimal inhibitory concentrations against these bacteria were 8-64 μg ml-1 for VAN and 512 μg ml-1 for GAL. The VAN plus GAL combination exhibited synergistic effects against E. faecium isolates, with a fraction inhibitory concentration index of 0.26-0.28. Time-kill assays confirmed this synergism. Mechanistic studies showed that the combination induced intracellular constituent leakage, suggesting impaired membrane permeability and electron microscopy revealed peptidoglycan and membrane damage. Additionally, the GAL plus VAN combination inhibited biofilm formation and significantly reduced lipid, protein, and carbohydrate contents, as shown by Fourier-transform infrared spectroscopy (FTIR).

CONCLUSIONS

GAL could reverse the activity of VAN against VREfm by damaging bacterial cell envelope, inhibiting biofilm formation, and reducing biomolecule contents, emphasizing its potential as a valuable adjunct to VAN in treating VREfm infections.

摘要

目的

屎肠球菌是全球范围内威胁人类健康的最重要的机会致病菌之一。对万古霉素(VAN)的耐药性正以惊人的速度增加。采用联合方法复活抗生素是一条有前景的替代途径。高良姜素(GAL)是一种存在于草药植物中的生物活性化合物。本研究旨在评估GAL与VAN联合对耐万古霉素屎肠球菌(VREfm)菌株的协同活性及作用方式。

方法与结果

VAN对这些细菌的最低抑菌浓度为8 - 64μg/ml,GAL为512μg/ml。VAN加GAL联合对屎肠球菌分离株表现出协同作用,部分抑菌浓度指数为0.26 - 0.28。时间杀菌试验证实了这种协同作用。机制研究表明,联合用药导致细胞内成分泄漏,提示膜通透性受损,电子显微镜显示肽聚糖和膜受损。此外,傅里叶变换红外光谱(FTIR)显示,GAL加VAN联合抑制生物膜形成,并显著降低脂质、蛋白质和碳水化合物含量。

结论

GAL可通过破坏细菌细胞壁、抑制生物膜形成和降低生物分子含量来逆转VAN对VREfm的活性,强调了其作为VAN治疗VREfm感染的有价值辅助药物的潜力。

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