State Key Laboratory of Oral Diseases & National Clinical Research Centre for Oral Disease, Sichuan University, Chengdu, China.
Department of Cariology and Endodontics West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Int Endod J. 2020 Jul;53(7):948-961. doi: 10.1111/iej.13296. Epub 2020 Apr 14.
The objectives of this laboratory-based study were to investigate the effects of GH12 on Enterococcus faecalis biofilm and virulence.
Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of GH12 against E. faecalis were first determined. A time-kill assay was further conducted. The effects of GH12 on the expression of virulence and stress genes in E. faecalis were evaluated by RT-qPCR. Crystal violet stain was used to investigate the effects of GH12 on E. faecalis biofilm formation and 1-day-old biofilm. Finally, an ex vivo tooth model contaminated with E. faecalis was used to evaluate the antimicrobial activity of GH12 as an irrigant by CFU counting, SEM and CLSM. One-way anova and Tukey's multiple comparisons test were used to compare the differences amongst groups (α = 0.05).
The MICs and MBCs of GH12 against E. faecalis were 8.0 ± 0.0 and 16.0 ± 0.0 mg L , respectively, and GH12 at 32.0 mg L reduced the bacterial numbers by more than 99.9% within 1 min. Various virulence genes (efaA, esp and gelE) and stress genes (dnaK, groEL, ctsR and clpPBCEX) in E. faecalis were significantly downregulated by GH12 at sub-MIC levels (P < 0.05). Additionally, both E. faecalis biofilm formation and the biomass of 1-day-old E. faecalis biofilm were significantly reduced by GH12 (P < 0.05). Elimination of E. faecalis in biofilms from root canal walls was achieved through irrigation with 64.0 mg L GH12 for 30 min. CLSM analysis revealed that GH12 at 64.0 mg L was most effective in eliminating bacteria within dentinal tubules (P < 0.05).
In a laboratory setting, and when used as an irrigant, GH12 suppressed E. faecalis, downregulated specific virulence and stress-associated genes, eliminated intracanal E. faecalis protected by biofilms and killed bacteria in dentinal tubules. These results emphasize the need for preclinical and clinical studies to explore the potential of GH12 as an antimicrobial agent during root canal treatment.
本实验室研究的目的是研究 GH12 对粪肠球菌生物膜和毒力的影响。
首先确定 GH12 对粪肠球菌的最小抑菌浓度(MIC)和最小杀菌浓度(MBC)。进一步进行时间杀伤试验。通过 RT-qPCR 评估 GH12 对粪肠球菌毒力和应激基因表达的影响。结晶紫染色法用于研究 GH12 对粪肠球菌生物膜形成和 1 天龄生物膜的影响。最后,使用体外牙模型污染粪肠球菌,通过 CFU 计数、SEM 和 CLSM 评估 GH12 作为冲洗液的抗菌活性。使用单因素方差分析和 Tukey 多重比较检验比较组间差异(α=0.05)。
GH12 对粪肠球菌的 MIC 和 MBC 分别为 8.0±0.0 和 16.0±0.0mg/L,GH12 在 32.0mg/L 时在 1 分钟内使细菌数量减少了 99.9%以上。粪肠球菌的各种毒力基因(efaA、esp 和 gelE)和应激基因(dnaK、groEL、ctsR 和 clpPBCEX)在亚 MIC 水平下均被 GH12 显著下调(P<0.05)。此外,GH12 还显著降低了粪肠球菌生物膜的形成和 1 天龄粪肠球菌生物膜的生物量(P<0.05)。通过用 64.0mg/L GH12 冲洗 30 分钟,从根管壁的粪肠球菌生物膜中消除了粪肠球菌。CLSM 分析显示,64.0mg/L 的 GH12 最有效地消除牙本质小管内的细菌(P<0.05)。
在实验室环境中,当用作冲洗液时,GH12 抑制粪肠球菌,下调特定的毒力和应激相关基因,消除生物膜保护的根管内粪肠球菌,并杀死牙本质小管内的细菌。这些结果强调了需要进行临床前和临床研究,以探索 GH12 在根管治疗期间作为抗菌剂的潜力。