Salli Krista M, Gürsoy Ulvi K, Söderling Eva M, Ouwehand Arthur C
DuPont Nutrition and Health, Global Health and Nutrition Science, Danisco Sweeteners Oy, 02460, Kantvik, Finland.
Department of Periodontology, Institute of Dentistry, University of Turku, Lemminkäisenkatu 2, 20520, Turku, Finland.
Curr Microbiol. 2017 Oct;74(10):1153-1159. doi: 10.1007/s00284-017-1299-6. Epub 2017 Jul 17.
Few laboratory methods exist for evaluating the cariogenicity of food ingredients. In this study, a dental simulator was used to determine the effects of commercial sucrose and xylitol mint products on the adherence and planktonic growth of Streptococcus mutans. Solutions (3% w/v) of sucrose, xylitol, sucrose mints, xylitol mints, xylitol with 0.02% peppermint oil (PO), and 0.02% PO alone were used to test the levels of planktonic and adhered S. mutans. A dental simulator with continuous artificial saliva flow, constant temperature, and mixing was used as a test environment and hydroxyapatite (HA) discs were implemented into the model to simulate the tooth surface. Bacterial content was quantified by qPCR. Compared with the artificial saliva alone, sucrose and sucrose mints increased the numbers of HA-attached S. mutans, whereas xylitol decreased them. Similarly, planktonic S. mutans quantities rose with sucrose and declined with xylitol and xylitol mints. Versus sucrose mints, xylitol mints significantly reduced the counts of HA-bound and planktonic S. mutans. Similar results were observed with the main ingredients of both types of mints separately. PO-supplemented artificial saliva did not influence the numbers of S. mutans that attached to HA or planktonic S. mutans compared with artificial saliva control. In our dental simulator model, xylitol reduced the counts of adhering and planktonic S.mutans. The mints behaved similarly as their pure, main ingredients-sucrose or xylitol, respectively. PO, which has been suggested to have antimicrobial properties, did not influence S. mutans colonization.
用于评估食品成分致龋性的实验室方法很少。在本研究中,使用牙科模拟器来确定市售蔗糖和木糖醇薄荷产品对变形链球菌黏附和浮游生长的影响。使用蔗糖、木糖醇、蔗糖薄荷糖、木糖醇薄荷糖、含0.02%薄荷油(PO)的木糖醇以及单独的0.02% PO的溶液(3% w/v)来测试浮游和黏附的变形链球菌水平。将具有连续人工唾液流动、恒温及混合功能的牙科模拟器用作测试环境,并在模型中植入羟基磷灰石(HA)盘以模拟牙齿表面。通过qPCR对细菌含量进行定量。与单独的人工唾液相比,蔗糖和蔗糖薄荷糖增加了HA黏附的变形链球菌数量,而木糖醇则减少了该数量。同样,浮游变形链球菌数量随蔗糖增加,随木糖醇和木糖醇薄荷糖减少。与蔗糖薄荷糖相比,木糖醇薄荷糖显著减少了HA结合和浮游的变形链球菌数量。分别对两种薄荷糖的主要成分进行测试时也观察到了类似结果。与人工唾液对照相比,添加PO的人工唾液对黏附于HA的变形链球菌数量或浮游变形链球菌数量没有影响。在我们的牙科模拟器模型中,木糖醇减少了黏附和浮游的变形链球菌数量。薄荷糖的作用与其纯主要成分(分别为蔗糖或木糖醇)相似。已表明具有抗菌特性的PO对变形链球菌定植没有影响。