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水合氯化小檗碱通过抑制分选酶A的活性来损害变形链球菌生物膜的形成。

Berberine chloride hydrate impairs Streptococcus mutans biofilm formation via inhibiting sortase A activity.

作者信息

Zhou Yang, Huang Fang, Lin Huancai

机构信息

Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-Sen University, Guangzhou, China.

Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-Sen University, Guangzhou, China.

出版信息

NPJ Biofilms Microbiomes. 2025 Jul 1;11(1):120. doi: 10.1038/s41522-025-00756-0.

Abstract

Dental caries is a biofilm-associated chronic progressive disease, results from the dissolution of mineralized tooth tissue by acidic generated from bacterial sugar fermentation. S. mutans, a prominent pathogen of dental caries, is acknowledged for its role in cariogenic biofilm formation, utilizing Sortase A (SrtA) to catalyse surface proteins, thus promoting biofilm formation. In our previous studies, the inhibitory effect of the berberine chloride hydrate (BH) on S. mutans biofilms was confirmed. Here, we further investigate the influence of BH on S. mutans biofilm-induced bovine enamel caries model and explore the effect of BH on S. mutans SrtA activity. We found that BH inhibited S. mutans biofilm formation in bovine enamel model, leading to a reduction in demineralization. Furthermore, we identified and characterized SrtA, which might catalyze SpaP of S. mutans to form fibrillar amyloid aggregates. Our findings showed that BH inhibited SrtA activity by binding to essential amino acid residues LEU-111, MET-123, and ARG-213. BH inhibited amyloid fibers formation by downregulating the expression of srtA gene, thus disrupting S. mutans biofilm formation. Taken together, our study provides new insight into the mechanism of antibiofilm activity of BH and reveals great potential for anticaries clinical applications.

摘要

龋齿是一种与生物膜相关的慢性进展性疾病,由细菌糖发酵产生的酸性物质溶解矿化牙组织所致。变形链球菌是龋齿的主要病原体,因其在致龋生物膜形成中的作用而受到认可,它利用分选酶A(SrtA)催化表面蛋白,从而促进生物膜形成。在我们之前的研究中,已证实盐酸小檗碱(BH)对变形链球菌生物膜具有抑制作用。在此,我们进一步研究BH对变形链球菌生物膜诱导的牛牙釉质龋模型的影响,并探讨BH对变形链球菌SrtA活性的作用。我们发现BH在牛牙釉质模型中抑制变形链球菌生物膜形成,导致脱矿减少。此外,我们鉴定并表征了SrtA,它可能催化变形链球菌的SpaP形成纤维状淀粉样聚集体。我们的研究结果表明,BH通过与必需氨基酸残基LEU-111、MET-123和ARG-213结合来抑制SrtA活性。BH通过下调srtA基因的表达来抑制淀粉样纤维的形成,从而破坏变形链球菌生物膜的形成。综上所述,我们的研究为BH的抗生物膜活性机制提供了新的见解,并揭示了其在抗龋临床应用中的巨大潜力。

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