Lam Anh K, Panlilio Hannah, Pusavat Jennifer, Wouters Cassandra L, Moen Erika L, Neel Andrew J, Rice Charles V
Department of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, 101 Stephenson Parkway, Norman, Oklahoma 73019, United States.
ACS Med Chem Lett. 2020 Mar 11;11(4):473-478. doi: 10.1021/acsmedchemlett.9b00595. eCollection 2020 Apr 9.
Methicillin-resistant (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 β-lactam potentiator against bacterial biofilms. Our previous study showed promise against methicillin-resistant 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.
耐甲氧西林金黄色葡萄球菌(MRSA)感染在全球构成严重威胁。MRSA是从与医疗设备相关的生物膜感染和慢性伤口中分离出的主要菌种。其形成生物膜的能力使其对市场上几乎所有抗生素都具有抗性。为响应替代治疗的需求,我们实验室一直在研究600 Da支链聚乙烯亚胺(BPEI)作为β-内酰胺增强剂对抗细菌生物膜的功效。我们之前的研究显示出对耐甲氧西林生物膜的治疗前景。本研究将我们之前的发现扩展到根除一种毒性更强的病原体:MRSA生物膜。微量滴定板最低生物膜根除浓度模型、结晶紫测定法和电子显微镜图像显示了BPEI与氨苄西林之间的协同作用,这是一种两步机制:第一步是去除细胞外聚合物(EPS)以暴露单个细菌靶点,第二步是BPEI与细胞壁中的阴离子磷壁酸发生静电相互作用以增强抗生素的作用。