Bao Jianhang, Huang Xinyan, Zeng Yan, Wu Tong Tong, Lu Xingyi, Meng Gina, Ren Yanfang, Xiao Jin
Eastman Institute for Oral Health, University of Rochester Medical Center, Rochester, NY 14642, USA.
School of Stomatology, Henan University, Zhengzhou 450046, China.
Pathogens. 2023 Jun 20;12(6):848. doi: 10.3390/pathogens12060848.
Dental caries is one of the most common chronic diseases worldwide. and are two major pathogens associated with dental caries. Several recent studies revealed that inhibits and in biofilms and in a rodent model of dental caries. The aim of this study was to investigate the dose-dependent effect of against and in a planktonic model that simulated a high-caries-risk clinical condition. Mono-, dual-, and multi-species models were utilized, with five doses of (ranging from 1.0 × 10 to 1.0 × 10 CFU/mL). Real-time PCR was used to assess the expression of the virulence genes of and and the genes of . Student's -tests and one-way ANOVA, followed by post hoc tests, were employed to compare the cell viability and gene expression among groups. A dose-dependent inhibition on and was observed with increased dosages of . at 10 CFU/mL demonstrated the highest antibacterial and antifungal inhibitory effect in the dual- and multi-species models. Specifically, at 20 h, the growth of and was suppressed by 1.5 and 5 logs, respectively ( < 0.05). The antifungal and antibacterial effects were attenuated in lower doses of (10-10 CFU/mL). The expression of and genes and and genes were significantly downregulated with an added 10 CFU/mL of ( < 0.05). The addition of 10 CFU/mL further inhibited the hyphae or pseudohyphae formation of . In summary, demonstrated dose-dependent antifungal and antibacterial effects against and . emerged as a promising candidate for the creation of novel antimicrobial probiotic products targeting dental caries prevention. Further research is warranted to identify the functional metabolites produced by at different dosages when interacting with and .
龋齿是全球最常见的慢性疾病之一。[具体细菌名称1]和[具体细菌名称2]是与龋齿相关的两种主要病原体。最近的几项研究表明,[某种物质]在生物膜和龋齿啮齿动物模型中可抑制[具体细菌名称1]和[具体细菌名称2]。本研究的目的是在模拟高龋齿风险临床状况的浮游模型中研究[某种物质]对[具体细菌名称1]和[具体细菌名称2]的剂量依赖性作用。使用了单物种、双物种和多物种模型,[某种物质]有五个剂量(范围从1.0×10到1.0×10 CFU/mL)。采用实时聚合酶链反应来评估[具体细菌名称1]和[具体细菌名称2]的毒力基因以及[其他相关基因名称]的基因表达。采用学生t检验和单因素方差分析,随后进行事后检验,以比较各组之间的细胞活力和基因表达。随着[某种物质]剂量的增加,观察到对[具体细菌名称1]和[具体细菌名称2]有剂量依赖性抑制作用。在双物种和多物种模型中,10 CFU/mL的[某种物质]表现出最高的抗菌和抗真菌抑制作用。具体而言,在20小时时,[具体细菌名称1]和[具体细菌名称2]的生长分别被抑制了1.5和5个对数(P<0.05)。较低剂量的[某种物质](10 - 10 CFU/mL)的抗真菌和抗菌作用减弱。添加10 CFU/mL的[某种物质]后,[具体细菌名称1]和[具体细菌名称2]的基因以及[其他相关基因名称]和[其他相关基因名称]的基因表达显著下调(P<0.05)。添加10 CFU/mL的[某种物质]进一步抑制了[某种真菌名称]的菌丝或假菌丝形成。总之,[某种物质]对[具体细菌名称1]和[具体细菌名称2]表现出剂量依赖性的抗真菌和抗菌作用。[某种物质]成为创建针对龋齿预防的新型抗菌益生菌产品的有希望的候选物。有必要进一步研究以确定[某种物质]在与[具体细菌名称1]和[具体细菌名称2]相互作用时不同剂量产生的功能代谢产物。