Department of Restorative Dentistry, Kanagawa Dental University, Yokosuka, Kanagawa, Japan.
Department of Oral Microbiology, Kanagawa Dental University, Yokosuka, Kanagawa, Japan.
Am J Dent. 2024 Feb;37(1):47-52.
To examine the relationship between remineralization of incipient root dentin lesions and the presence of polymicrobial biofilms, as well as examine changes in microbial composition.
Bovine root dentin disks used as specimens for biofilm formation, were cultured using saliva from a single donor. Amsterdam Active Attachment biofilm model was used to grow biofilms. The culture medium was McBain 2005 with 0.2% sucrose and 0.4 ppm F as sodium fluoride. After cultivation for 48 hours to achieve demineralization, a control group (n=10) was obtained and the other specimens were further cultured for 336 hours in two types of remineralization culture medium, with sucrose (S+) and without sucrose (S-), through continuous anaerobic incubation (10% CO2,10% H2, 80% N2). Then half of the specimens cultured in the S- medium were transferred to the S+ medium for an additional 48 hours resulting in three experimental groups S(+) (n=10), S(-) (n=10), and S(-)de (n=10), respectively. Experiment 1: Transverse microradiography (TMR) analysis - Immediately after respective culture treatments, integrated mineral loss (IML) and lesion depth (LD) in the dentin specimens were analyzed by TMR. Experiment 2: Microbiome analysis - Sequence data of the 16S rRNA gene of each sample was obtained using MiSeq, and partial base sequences were determined. Next-generation sequencing was performed to determine the taxonomic groups of fungi present in the biofilm samples.
Experiment 1: In the control group, formation of dentin demineralization lesions by polymicrobial species biofilms was confirmed. The S(-) group showed significantly decreased IML and shallower LD compared to the control group. The S(-)de group showed a significant increase in IML and LD compared to the S(-) group. Experiment 2: There were statistically significant differences in microbiome between the control group and each of the three experimental groups, both at the genus and species levels. A significant difference in genus was observed between the S(-) group and the S(-)de group.
The confirmation of the possibility of microbial shift occurring during the remineralization process of root caries will lead to the development of new remineralization therapies.
研究初期牙本质龋再矿化与多微生物生物膜的关系,并观察微生物组成的变化。
使用来自单个供体的唾液培养牛牙本质圆盘作为生物膜形成的标本。使用阿姆斯特丹主动附着生物膜模型培养生物膜。培养基为 McBain 2005 加 0.2%蔗糖和 0.4ppm F 作为氟化钠。培养 48 小时达到脱矿后,获得对照组(n=10),然后将其余标本在两种再矿化培养基中进一步培养 336 小时,一种含有蔗糖(S+),另一种不含蔗糖(S-),通过连续厌氧孵育(10%CO2、10%H2、80%N2)。然后,将 S-培养基培养的一半标本转移到 S+培养基中再培养 48 小时,分别得到三个实验组 S(+)(n=10)、S(-)(n=10)和 S(-)de(n=10)。实验 1:横向显微放射摄影术(TMR)分析 - 在各自的培养处理后立即分析牙本质标本的整体矿物质损失(IML)和病变深度(LD)。实验 2:微生物组分析 - 使用 MiSeq 获得每个样本的 16S rRNA 基因的序列数据,并确定部分碱基序列。进行下一代测序以确定生物膜样本中真菌的分类群。
实验 1:在对照组中,证实了多微生物物种生物膜形成牙本质脱矿病变。与对照组相比,S(-)组的 IML 显著降低,LD 变浅。与 S(-)组相比,S(-)de 组的 IML 和 LD 显著增加。实验 2:在属和种水平上,对照组与三个实验组中的每一个之间的微生物组都存在统计学上的显著差异。在 S(-)组和 S(-)de 组之间观察到属水平的显著差异。
确认根面龋再矿化过程中微生物转移的可能性,将导致新的再矿化治疗方法的发展。