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Low-Molecular-Weight Branched Polyethylenimine Potentiates Ampicillin against MRSA Biofilms

机译:低分子量支链聚乙烯亚胺增强氨苄青霉素对阵MRSA生物膜

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Methicillin-resistant Staphylococcus aureus (MRSA) infections pose a serious threat worldwide. MRSA is the predominant species isolated from medical-device-related biofilm infections and chronic wounds. Its ability to form biofilms grants it resistance to almost all antibiotics on the market. Answering the call for alternative treatments, our lab has been investigating the efficacy of 600 Da branched polyethylenimine (BPEI) as a beta-lactam potentiator against bacterial biofilms. Our previous study showed promise against methicillin-resistant Staphylococcus epidermidis biofilms. This study extends our previous findings to eradicate a more virulent pathogen: MRSA biofilms. Microtiter minimum biofilm eradication concentration models, crystal violet assays, and electron microscopy images show synergistic effects between BPEI and ampicillin as a two-step mechanism: step one is the removal of the extracellular polymeric substances (EPS) to expose individual bacteria targets, and step two involves electrostatic interaction of BPEI with anionic teichoic acid in the cell wall to potentiate the antibiotic.
机译:耐甲氧西林金黄色葡萄球菌(MRSA)感染构成全世界严重威胁。 MRSA是与医疗器械相关的生物膜感染和慢性伤口分离的主要物种。它能够形成生物膜的能力给它抵抗几乎所有抗生素的市场。回答替代治疗的呼吁,我们的实验室已经研究了600A分支聚乙烯亚胺(BPEI)作为β-内酰胺增强剂对细菌生物膜的效果。我们以前的研究表明,对耐甲虫耐甲虫的葡萄球菌癫痫生物膜有望。本研究扩展了我们以前的发现,以消除更加毒性的病原体:MRSA生物膜。微量滴定剂最小生物膜消除浓度模型,晶体紫色测定和电子显微镜图像在BPEI和氨苄青霉素之间表现出协同作用,作为两步机制:步骤一步是去除细胞外聚合物物质(EPS)以暴露单个细菌靶点,以及步骤尤涉及BPEI与细胞壁中阴离子噻吩的静电相互作用,以提高抗生素。

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