Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, 14176-14411 Tehran, Iran.
Department of Pediatric Dentistry, Faculty of Dentistry, Shahed University, 14177-55351 Tehran, Iran.
Front Biosci (Landmark Ed). 2023 May 9;28(5):88. doi: 10.31083/j.fbl2805088.
is a major component of dental plaque, contributing to cariogenic biofilm formation and inducing dental caries. Attempts have recently been made to use postbiotic mediators (PMs) to prevent dental caries. This research evaluated the antimicrobial/antibiofilm activity of PMs derived from GG (LGG) and (LR) against .
PMs were obtained from the supernatants. The minimum inhibitory concentration, minimum bactericidal concentration, antibiofilm potential, and metabolic activity of PMs against were evaluated using CFU/mL, scanning electron microscopy, and XTT (2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide) reduction assay. The expression of gene as one of the most important genes involved in biofilm formation was also measured using qRT-PCR.
CFU score was reduced by both PMs, but the reduction was only significant in LGG ( = 0.02). Both PMs caused a significant decrease in the metabolic activity of compared with the controls ( ≤ 0.002). treated with LGG PMs exhibited more destructive effects than LR PMs ( > 0.05). gene expression was significantly downregulated when treated with the PMs obtained from both LGG and LR ( = 0.01 for both).
We showed that PMs isolated from two strains inhibited biofilm, metabolic activity, and gene expression. Therefore, these derivatives may be a suitable biofilm-destruction agent against . However, the oral environment is a complex ecosystem that needs further investigation.
是牙菌斑的主要成分,有助于致龋生物膜的形成,并导致龋齿。最近有人试图使用后生元调节剂(PMs)来预防龋齿。本研究评估了源自 GG(LGG)和 (LR)的 PMs 对 的抗菌/抗生物膜活性。
从 上清液中获得 PMs。使用 CFU/mL、扫描电子显微镜和 XTT(2,3-双-(2-甲氧基-4-硝基-5-磺苯基)-2H-四唑-5-羧基苯胺)还原测定法评估 PMs 对 的最小抑菌浓度、最小杀菌浓度、抗生物膜潜力和代谢活性。还使用 qRT-PCR 测量了作为参与 生物膜形成的最重要基因之一的 基因的表达。
两种 PMs 均降低了 CFU 评分,但仅在 LGG 中降低具有统计学意义(=0.02)。与对照组相比,两种 PMs 均显著降低 代谢活性(≤0.002)。与 LR PMs 相比,用 LGG PMs 处理的 表现出更具破坏性的影响(>0.05)。用 LGG 和 LR 来源的 PMs 处理后, 基因表达均显著下调(=0.01)。
我们表明,从两种 菌株中分离出的 PMs 抑制了 生物膜、代谢活性和 基因表达。因此,这些衍生物可能是一种针对 的合适的生物膜破坏剂。然而,口腔环境是一个复杂的生态系统,需要进一步研究。