State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Cariology and Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Laboratory of Human Disease and Immunotherapies, West China Hospital, Sichuan University, Chengdu, China.
Biomed Res Int. 2020 Nov 20;2020:8379526. doi: 10.1155/2020/8379526. eCollection 2020.
Disruption of microbial biofilms is an effective way to control dental caries. Drug resistance and side effects of the existing antimicrobials necessitate the development of novel antibacterial agents. The current study was aimed at investigating the antibacterial activities of the repurposed natural compound napabucasin against oral streptococci.
The minimum inhibitory concentration, minimum bactericidal concentration, minimum biofilm inhibition concentration, and minimum biofilm reduction concentration of , , and were examined by a microdilution method. Cytotoxicity of napabucasin against human oral keratinocytes, human gingival epithelia, and macrophage RAW264.7 was evaluated by CCK8 assays. The dead/live bacterium and exopolysaccharide in the napabucasin-treated multispecies biofilms were evaluated by confocal laser scanning microscopy. Microbial composition within the napabucasin-treated biofilms was further visualized by fluorescent in situ hybridization and qPCR. And the cariogenicity of napabucasin-treated biofilms was evaluated by transverse microradiography.
Napabucasin exhibited good antimicrobial activity against oral streptococcal planktonic cultures and biofilms but with lessened cytotoxicity as compared to chlorhexidine. Napabucasin reduced the cariogenic and increased the proportion of the commensal in the multispecies biofilms. More importantly, napabucasin significantly reduced the demineralization capability of biofilms on tooth enamels.
Napabucasin shows lessened cytotoxicity and comparable antimicrobial effects to chlorhexidine. Repurposing napabucasin may represent a promising adjuvant for the management of dental caries.
破坏微生物生物膜是控制龋齿的有效方法。现有抗菌药物的耐药性和副作用促使人们开发新型抗菌剂。本研究旨在研究重用途天然化合物萘泊沙司他对口腔链球菌的抗菌活性。
采用微量稀释法检测 、 、 和 的最小抑菌浓度、最小杀菌浓度、最小生物膜抑制浓度和最小生物膜减少浓度。通过 CCK8 测定法评估萘泊沙司他对人口腔角质形成细胞、人牙龈上皮细胞和巨噬细胞 RAW264.7 的细胞毒性。通过共聚焦激光扫描显微镜评估萘泊沙司他处理的多物种生物膜中的死/活菌和胞外多糖。通过荧光原位杂交和 qPCR 进一步观察萘泊沙司他处理的生物膜中的微生物组成。通过横向显微放射摄影术评估萘泊沙司他处理的生物膜的致龋性。
萘泊沙司他对口腔链球菌浮游培养物和生物膜表现出良好的抗菌活性,但与洗必泰相比,细胞毒性降低。萘泊沙司他减少了多物种生物膜中的致龋 ,增加了共生 的比例。更重要的是,萘泊沙司他显著降低了生物膜在牙釉质上的脱矿能力。
萘泊沙司他的细胞毒性降低,抗菌效果与洗必泰相当。重新利用萘泊沙司他可能代表了一种有前途的辅助治疗龋齿的方法。