Kim Hye-Ji, Yoo Hyun-Jun
Department of Dental Hygiene, College of Health Science, Dankook University, Cheonan, Republic of Korea.
Department of Preventive Dentistry, College of Dentistry, Dankook University, Cheonan, Republic of Korea.
J Dent Sci. 2023 Jan;18(1):65-72. doi: 10.1016/j.jds.2022.07.011. Epub 2022 Aug 5.
BACGROUND/PURPOSE: () K12 is known to be a probiotic bacterium. The purpose of this study was to investigate anti-cariogenic effects of K12 on cariogenic biofilm.
K12 was cultured in M17 broth. The antimicrobial activity of spent culture medium (SCM) against was investigated. K12 was co-cultivated with using a membrane insert. When the biofilm was formed using salivary bacteria and , the K12 was inoculated every day. The biomass of biofilm was investigated by a confocal laser scanning microscope. Also, bacterial DNA from the biofilm was extracted, and then bacteria proportion was analyzed by quantitative PCR using specific primers. The expression of genes of in the biofilm with or without K12 was analyzed by RT-PCR.
The SCM of K12 inhibited the growth of . Also, K12 reduced growth in co-cultivation. The formation of cariogenic biofilm was reduced by adding K12, and the count of in the biofilm was also decreased in the presence of K12. B, C, and D expression of in the biofilm was reduced in the presence of K12.
K12 may inhibit the formation of cariogenic biofilm by interrupting the growth and glucosyltransferase production of .
背景/目的:已知K12是一种益生菌。本研究的目的是调查K12对致龋生物膜的抗龋作用。
K12在M17肉汤中培养。研究了用过的培养基(SCM)对(此处原文缺失相关内容)的抗菌活性。使用膜插入物将K12与(此处原文缺失相关内容)共培养。当使用唾液细菌和(此处原文缺失相关内容)形成生物膜时,每天接种K12。通过共聚焦激光扫描显微镜研究生物膜的生物量。此外,从生物膜中提取细菌DNA,然后使用特异性引物通过定量PCR分析细菌比例。通过RT-PCR分析有或没有K12的生物膜中(此处原文缺失相关内容)基因的表达。
K12的SCM抑制了(此处原文缺失相关内容)的生长。此外,K12在共培养中减少了(此处原文缺失相关内容)的生长。添加K12可减少致龋生物膜的形成,并且在存在K12的情况下生物膜中(此处原文缺失相关内容)的数量也减少。在存在K12的情况下,生物膜中(此处原文缺失相关内容)的B、C和D表达降低。
K12可能通过中断(此处原文缺失相关内容)的生长和葡糖基转移酶的产生来抑制致龋生物膜的形成。