Freelance Researcher, Crotone, Italy.
IRCCS Orthopedic Institute Galeazzi, Milan, Italy.
Odontology. 2020 Jul;108(3):396-405. doi: 10.1007/s10266-020-00499-8. Epub 2020 Feb 28.
This study aimed to evaluate the antimicrobial and antibiofilm activity of two chelating agents: ethylenediaminetetraacetic acid (EDTA) combined or not with detergents, and etidronic acid combined with sterile saline. The bacterial inhibitory and bactericidal concentrations (MIC and MBC, respectively) were determined on Enterococcus faecalis ATCC 4083 strain. Antimicrobial tests were performed on a biofilm model after treatment with the chelating agents at different times (1, 3, and 5 min) using a biofilm eradication concentration (MBEC) and confocal laser scanning microscope (CLSM) assays. Quantification of cell biomass and percentage of live and dead cells in the biomass was assessed for each group. The normality of the distributions for each variable was assessed using the D'Agostino and Pearson's omnibus normality test. The comparison of bacterial viability among groups and between any two groups was performed using the non-parametric Kruskal-Wallis one-way analysis of variance and the Dunn's test, respectively. No significant between-group difference was observed regarding biomass reduction. On the other hand, EDTA combined with detergents displayed a substantial increase of the dead bacteria ranging between 35 and 43%; whereas, the number of cells killed in the control group and in the other treated groups always ranged between 1 and 6%, at all experimental times. The addition of detergents to EDTA can improve its anti-biofilm activity by reducing EPS production and enhancing the killing of sessile bacterial cells. Clinical relevance EDTA presents a relevant antimicrobial activity when combined with surface-active agents.
乙二胺四乙酸(EDTA)与表面活性剂联合或不联合,以及依替膦酸与无菌生理盐水联合。采用肉汤微量稀释法,分别测定粪肠球菌 ATCC 4083 株的最低抑菌浓度(MIC)和最低杀菌浓度(MBC)。在不同时间(1、3 和 5 分钟)用螯合剂处理生物膜模型后,采用生物膜清除浓度(MBEC)和共聚焦激光扫描显微镜(CLSM)试验,进行抗菌试验。对每组生物膜的细胞生物量和活细胞与死细胞在生物量中的百分比进行定量评估。采用 D'Agostino 和 Pearson 整体正态性检验评估各变量的分布正态性。采用非参数 Kruskal-Wallis 单向方差分析和 Dunn 检验分别比较各组间和任意两组间细菌活力的差异。各组间生物量减少无显著差异。另一方面,EDTA 与表面活性剂联合使用可显著增加死菌数量,范围在 35%至 43%之间;而在对照组和其他处理组中,所有实验时间的活菌数量始终在 1%至 6%之间。表面活性剂的加入可通过减少 EPS 的产生和增强对固定细菌细胞的杀伤作用来提高 EDTA 的抗生物膜活性。临床意义 EDTA 与表面活性剂联合具有重要的抗菌活性。