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Synergy between Ursolic and Oleanolic Acids from Vitellaria paradoxa Leaf Extract and -Lactams against Methicillin-Resistant Staphylococcus aureus: In Vitro and In Vivo Activity and Underlying Mechanisms

机译:来自Vitellaria悖论叶提取物和抗甲氧西林金黄色葡萄球菌的甲酰胺酸和蛋白酰胺的协同作用:体外和体内活性和潜在机制

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摘要

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 -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 -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 -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-1) production. Thus, these data highlight the potential interest of triterpenic acids as resistance reversing agents in combination with -lactams against MRSA.
机译:将抗生素与抗性逆转剂结合起来是克服细菌抗性的关键策略。在筛查传统医学中使用的植物的抗菌活性后,我们发现来自乳木叶(Vitellaria paradoxa)的叶片二氯甲烷提取物对甲氧西林抗性金黄色葡萄球菌(MRSA)的抗微生物活性,并在与 - 酰胺结合时进一步证据了协同作用。使用HPLC-MS,我们在该物种的叶片和叶片中鉴定了铀酸(UA)和oA),并通过HPLC-UV定量为叶子提取物中的主要成分(分别为21%和6%)。纯三萜酸两者都显示出抗微生物活性对抗MRSA的参考和临床菌株,MICS为OA的UA至32-128mg / L的8-16 mg / L.它们在脑子浓度下与 - 酰胺(氨苄青霉素和恶毒藻蛋白)具有高度协同作用。 MRSA表型的恢复归因于它们将PBP2从隔膜分裂部位删除PBP2的能力,如荧光显微镜观察到的,并打扰从而肽聚糖合成。此外,两种化合物也抑制了活细菌的酰胺酶活性(如抑制硝基孔水解的评估),但不在细菌裂解物中,表明这种抑制的间接机制。在皮下MRSA感染的小鼠模型中,局部施用UA与Nafcillin协同作用,以降低病变大小和炎症细胞因子(IL-1)的生产。因此,这些数据突出了三萜酸作为抗性逆转剂与-lactams对抗MRSA的潜在兴趣。

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