甘草香豆素体外抗金黄色葡萄球菌生物膜效应

In vitro effect of glycycoumarin against Staphylococcus aureus biofilm

  • 摘要:
    目的 评估植物甘草香豆素对金黄色葡萄球菌的抑菌及抗生物膜作用, 为临床抗金黄色葡萄球菌感染药物的开发和应用奠定基础。
    方法 测定甘草香豆素对金黄色葡萄球菌的最小抑菌浓度(MIC)与最小杀菌浓度(MBC);绘制生长曲线观察不同浓度甘草香豆素对细菌生长的影响;通过结晶紫染色法检测甘草香豆素对金黄色葡萄球菌生物膜形成的影响及对成熟生物膜的清除作用。
    结果 甘草香豆素对金黄色葡萄球菌的MIC与MBC均为4 μg/ml;生长曲线提示对细菌抑制效果与药物浓度呈正相关, 当甘草香豆素浓度为0.5 μg/ml时, 即有明显抑菌效果, 浓度为4 μg/ml时, 可完全抑制金黄色葡萄球菌的生长;抑制生物膜形成所需药物浓度与抑制浮游菌的药物浓度相同, 金黄色葡萄球菌生物膜以剂量依赖性方式形成;16 μg/ml时对成熟生物膜的清除作用达到80.47%。
    结论 甘草香豆素对浮游状态金黄色葡萄球菌有良好抑菌作用, 首次揭示了其对生物膜形成和成熟生物膜有清除能力。此文为治疗顽固性生物膜相关感染提供了新的思路。

     

    Abstract:
    OBJECTIVE To evaluate the antibacterial and anti-biofilm effects of the plant-derived glycycoumarin against Staphylococcus aureus, laying a foundation for the development and application of drugs for clinical treatment of S. aureus infection.
    METHODS The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of glycycoumarin against S. aureus were determined. Growth curves were plotted to observe the impact of different concentrations of glycycoumarin on bacterial growth. The effect of glycycoumarin on S. aureus biofilm formation and mature biofilms eradication were assessed through the crystal violet staining method.
    RESULTS The MIC and MBC of glycycoumarin against S. aureus were both 4 μg/ml. Growth curves indicated that the inhibitory effect on bacteria was positively correlated with drug concentration. Significant antibacterial effects were observed at a glycycoumarin concentration of 0.5 μg/ml, and complete inhibition of S. aureus growth was achieved at 4 μg/ml. The drug concentration required for inhibiting biofilm formation was the same as that for inhibiting planktonic bacteria. S. aureus biofilms formed in a dose-dependent manner, and at 16 μg/ml, glycycoumarin achieved an 80.47% eradication of mature biofilms.
    CONCLUSIONS Glycycoumarin exhibits good antibacterial activity against planktonic S. aureus, and for the first time its ability to inhibit biofilm formation and eradicate mature biofilms was demonstrated. This study provides new insights for the treatment of recalcitrant biofilm-associated infection.

     

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