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首页> 外文期刊>Molecules >Synergy between Ursolic and Oleanolic Acids from Vitellaria paradoxa Leaf Extract and β-Lactams against Methicillin-Resistant Staphylococcus aureus: In Vitro and In Vivo Activity and Underlying Mechanisms
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Synergy between Ursolic and Oleanolic Acids from Vitellaria paradoxa Leaf Extract and β-Lactams against Methicillin-Resistant Staphylococcus aureus: In Vitro and In Vivo Activity and Underlying Mechanisms

机译:tell蚕丝叶提取物中熊果酸和齐墩果酸与β-内酰胺对耐甲氧西林金黄色葡萄球菌的协同作用:体内和体外活性及潜在机制

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Combining antibiotics with resistance reversing agents is a key strategy to overcome bacterial resistance. Upon screening antimicrobial activities of plants used in traditional medicine, we found that a leaf dichloromethane extract from the shea butter tree (Vitellaria paradoxa) had antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA) with further evidence of synergy when combined with β-lactams. Using HPLC-MS, we identified ursolic (UA) and oleanolic acids (OA) in leaves and twigs of this species, and quantified them by HPLC-UV as the major constituents in leaf extracts (21% and 6% respectively). Both pure triterpenic acids showed antimicrobial activity against reference and clinical strains of MRSA, with MICs ranging from 8–16 mg/L for UA to 32–128 mg/L for OA. They were highly synergistic with β-lactams (ampicillin and oxacillin) at subMIC concentrations. Reversion of MRSA phenotype was attributed to their capacity to delocalize PBP2 from the septal division site, as observed by fluorescence microscopy, and to disturb thereby peptidoglycan synthesis. Moreover, both compounds also inhibited β-lactamases activity of living bacteria (as assessed by inhibition of nitrocefin hydrolysis), but not in bacterial lysates, suggesting an indirect mechanism for this inhibition. In a murine model of subcutaneous MRSA infection, local administration of UA was synergistic with nafcillin to reduce lesion size and inflammatory cytokine (IL-1β) production. Thus, these data highlight the potential interest of triterpenic acids as resistance reversing agents in combination with β-lactams against MRSA. View Full-Text
机译:结合抗生素和耐药逆转剂是克服细菌耐药性的关键策略。通过筛选传统药物中的植物的抗菌活性,我们发现乳木果油树(Vitellaria paradoxa)的二氯甲烷叶提取物对耐甲氧西林的金黄色葡萄球菌(MRSA)具有抗菌活性,与β-内酰胺类药物合用时可进一步证明具有协同作用。 。使用HPLC-MS,我们鉴定了该物种的叶片和嫩枝中的熊果酚(UA)和齐墩果酸(OA),并通过HPLC-UV对其进行了定量,以确定叶提取物中的主要成分(分别为21%和6%)。两种纯三萜酸均显示出对参考和临床MRSA菌株的抗菌活性,MIC的范围从UA的8–16 mg / L到OA的32–128 mg / L。在亚MIC浓度下,它们与β-内酰胺类(氨苄青霉素和奥沙西林)高度协同。 MRSA表型的逆转归因于其使PBP2从间隔分裂位点脱离定位的能力(如荧光显微镜所观察到的),从而干扰了肽聚糖的合成。而且,这两种化合物也都抑制活细菌的β-内酰胺酶活性(通过抑制nitrocefin水解来评估),但在细菌裂解物中却没有,这表明这种抑制作用的间接机制。在皮下MRSA感染的小鼠模型中,UA的局部给药与萘夫西林具有协同作用,以减少病变大小和炎性细胞因子(IL-1β)的产生。因此,这些数据突出了三萜酸作为抗逆剂与β-内酰胺类药物联合对抗MRSA的潜在兴趣。查看全文

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