Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Nat Protoc. 2021 May;16(5):2615-2632. doi: 10.1038/s41596-021-00515-3. Epub 2021 Apr 28.
Bacterial biofilms demonstrate high broad-spectrum adaptive antibiotic resistance and cause two thirds of all infections, but there is a lack of approved antibiofilm agents. Unlike the standard minimal inhibitory concentration assay to assess antibacterial activity against planktonic cells, there is no standardized method to evaluate biofilm inhibition and/or eradication capacity of novel antibiofilm compounds. The protocol described here outlines simple and reproducible methods for assessing the biofilm inhibition and eradication capacities of novel antibiofilm agents against adherent bacterial biofilms grown in 96-well microtiter plates. It employs two inexpensive dyes: crystal violet to stain adhered biofilm biomass and 2,3,5-triphenyl tetrazolium chloride to quantify metabolism of the biofilm cells. The procedure is accessible to any laboratory with a plate reader, requires minimal technical expertise or training and takes 4 or 5 d to complete. Recommendations for how biofilm inhibition and eradication results should be interpreted and presented are also described.
细菌生物膜表现出广谱的高度适应性抗生素耐药性,导致三分之二的感染,但目前缺乏经过批准的抗生物膜药物。与评估抗浮游细胞活性的标准最小抑菌浓度测定法不同,目前还没有标准化的方法来评估新型抗生物膜化合物的生物膜抑制和/或清除能力。本文描述的方案概述了简单且可重复的方法,用于评估在 96 孔微量滴定板中生长的粘附性细菌生物膜的新型抗生物膜剂的生物膜抑制和清除能力。它使用两种廉价的染料:结晶紫染色附着的生物膜生物量和 2,3,5-三苯基氯化四氮唑定量测定生物膜细胞的代谢。该程序可供任何具有平板读数器的实验室使用,需要最少的技术专业知识或培训,并且需要 4 或 5 天才能完成。还描述了如何解释和呈现生物膜抑制和清除结果的建议。