Shao Yidan, Zhu Wenyan, Liu Shanshan, Zhang Kai, Sun Yu, Liu Yudong, Wen Tingchi, Zou Yingxue, Zheng Qingwei
Anhui Key Laboratory of Infection and Immunity, Bengbu Medical University, 2600 Dong Hai Avenue, Bengbu, 233030, China.
Department of Stomatology, The First Affiliated Hospital of Bengbu Medical University, 287 Chuang Huai Road, Bengbu, 233004, China.
BMC Oral Health. 2025 Jan 4;25(1):25. doi: 10.1186/s12903-024-05355-7.
Streptococcus mutans (S. mutans) contributes to caries. The biofilm formed by S. mutans exhibits greater resistance to drugs and host immune defenses than the planktonic form of the bacteria. The objective of this study was to evaluate the anti-biofilm effect of cordycepin from the perspective of metabolomics.
The minimum inhibitory concentration (MIC) was determined to evaluate the antimicrobial effect of cordycepin on planktonic S. mutans. The 24-h biofilm was treated with 128 µg/mL of cordycepin for 10 min at the 8- or 20-h time points. Biofilm biomass and metabolism were assessed using crystal violet and MTT assays and cordycepin cytotoxicity was evaluated in human oral keratinocytes (HOK) using CCK-8 assays. The live bacterial rate and the biofilm volume were assessed by confocal laser scanning microscopy. Metabolic changes in the biofilm collected at different times during with cordycepin were analyzed by metabolomics and verified by quantitative real-time PCR.
The results showed that treatment with 128 µg/mL cordycepin reduced both the biomass and metabolic activity of the biofilm without killing the bacteria, and cordycepin at this concentration showed good biocompatibility. Metabolomics analysis showed that differentially abundant metabolites following cordycepin treatment were mainly related to purine and nucleotide metabolism. After immediate treatment with cordycepin, genes related to purine and nucleotide metabolism were downregulated, and the levels of various metabolites changed significantly. However, the effect was reversible. After continuing culture for 4 h, the changes in genes and most metabolites were reversed, although the levels of 2'-deoxyadenosine, 2'-deoxyinosine, and adenine remained significantly different.
Cordycepin has the effect of anti-biofilm of S. mutans, mainly related to purine and nucleotide metabolism.
变形链球菌(S. mutans)会导致龋齿。变形链球菌形成的生物膜比该细菌的浮游形式对药物和宿主免疫防御具有更强的抵抗力。本研究的目的是从代谢组学角度评估虫草素的抗生物膜作用。
测定最低抑菌浓度(MIC)以评估虫草素对浮游变形链球菌的抗菌作用。在8小时或20小时时间点,用128μg/mL虫草素处理24小时生物膜10分钟。使用结晶紫和MTT法评估生物膜生物量和代谢情况,并使用CCK-8法在人口腔角质形成细胞(HOK)中评估虫草素的细胞毒性。通过共聚焦激光扫描显微镜评估活菌率和生物膜体积。对虫草素处理过程中不同时间收集的生物膜的代谢变化进行代谢组学分析,并通过定量实时PCR进行验证。
结果表明,用128μg/mL虫草素处理可降低生物膜的生物量和代谢活性,且不会杀死细菌,该浓度的虫草素具有良好的生物相容性。代谢组学分析表明,虫草素处理后差异丰富的代谢物主要与嘌呤和核苷酸代谢有关。用虫草素立即处理后,与嘌呤和核苷酸代谢相关的基因下调,各种代谢物水平发生显著变化。然而,这种作用是可逆的。继续培养4小时后,基因和大多数代谢物的变化被逆转,尽管2'-脱氧腺苷、2'-脱氧肌苷和腺嘌呤的水平仍存在显著差异。
虫草素具有抗变形链球菌生物膜的作用,主要与嘌呤和核苷酸代谢有关。