Robertson Shaun N, Childs Peter G, Akinbobola Ayorinde, Henriquez Fiona L, Ramage Gordon, Reid Stuart, Mackay William G, Williams Craig
Institute of Healthcare, Policy and Practice, School of Health & Life Sciences, University of the West of Scotland, High Street, Paisley PA1 2BE, Scotland, UK; SUPA, Institute of Thin Films, Sensors and Imaging, School of Engineering and Computing, University of the West of Scotland, High Street, Paisley PA1 2BE, Scotland, UK; SUPA, Department of Biomedical Engineering, University of Strathclyde, 40 George Street, Glasgow G1 1QE, Scotland, UK.
SUPA, Institute of Thin Films, Sensors and Imaging, School of Engineering and Computing, University of the West of Scotland, High Street, Paisley PA1 2BE, Scotland, UK; Centre for the Cellular Microenvironments (CeMi), School of Engineering, University of Glasgow, G12 8LT, Scotland, UK.
J Biosci Bioeng. 2020 Mar;129(3):379-386. doi: 10.1016/j.jbiosc.2019.09.003. Epub 2019 Oct 15.
Bacterial biofilms pose a significant burden in both healthcare and industrial environments. With the limited effectiveness of current biofilm control strategies, novel or adjunctive methods in biofilm control are being actively pursued. Reported here, is the first evidence of the application of nanovibrational stimulation (nanokicking) to reduce the biofilm formation of Pseudomonas aeruginosa. Nanoscale vertical displacements (approximately 60 nm) were imposed on P. aeruginosa cultures, with a significant reduction in biomass formation observed at frequencies between 200 and 4000 Hz at 24 h. The optimal reduction of biofilm formation was observed at 1 kHz, with changes in the physical morphology of the biofilms. Scanning electron microscope imaging of control and biofilms formed under nanovibrational stimulation gave indication of a reduction in extracellular matrix (ECM). Quantification of the carbohydrate and protein components of the ECM was performed and showed a significant reduction at 24 h at 1 kHz frequency. To model the forces being exerted by nanovibrational stimulation, laser interferometry was performed to measure the amplitudes produced across the Petri dish surfaces. Estimated peak forces on each cell, associated with the nanovibrational stimulation technique, were calculated to be in the order of 10 pN during initial biofilm formation. This represents a potential method of controlling microbial biofilm formation in a number of important settings in industry and medical related processes.
细菌生物膜在医疗保健和工业环境中都构成了重大负担。鉴于当前生物膜控制策略的效果有限,人们正在积极探索生物膜控制的新方法或辅助方法。本文报道了首次应用纳米振动刺激(纳米踢动)来减少铜绿假单胞菌生物膜形成的证据。对铜绿假单胞菌培养物施加纳米级垂直位移(约60纳米),在24小时时,观察到在200至4000赫兹的频率下生物量形成显著减少。在1千赫兹时观察到生物膜形成的最佳减少效果,同时生物膜的物理形态也发生了变化。对对照生物膜和在纳米振动刺激下形成的生物膜进行扫描电子显微镜成像,结果表明细胞外基质(ECM)减少。对ECM的碳水化合物和蛋白质成分进行了定量分析,结果显示在1千赫兹频率下24小时时显著减少。为了模拟纳米振动刺激所施加的力,进行了激光干涉测量以测量培养皿表面产生的振幅。在生物膜初始形成过程中,与纳米振动刺激技术相关的每个细胞上估计的峰值力经计算约为10皮牛。这代表了一种在工业和医疗相关过程中的许多重要场景中控制微生物生物膜形成的潜在方法。