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Studies on antimicrobial activity of Poncirus trifoliata ethyl extract fraction against methicillin-resistant Staphylococcus aureus and to elucidate its antibacterial mechanism

机译:三角叶乙基提取物组分对耐甲氧西林金黄色葡萄球菌的抗菌活性及其抗菌机理的研究

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摘要

Traditional medicinal plants contain a wide variety of chemicals that have potent antibacterial activity. To find an alternative agent of overcoming the problems of methicillin-resistant Staphylococcus aureus (MRSA), the antibacterial mechanism of Ponciruss trifoliata against MRSA was investigated. Ethyl acetate (EtOAc)-soluble extract of P. trifoliata methanolic extract was evaluated for antibacterial activity using minimum inhibitory concentration (MIC). An EtOAc sub-fraction 08 (EA08) from silica-gel open column chromatography exhibited strong anti-MRSA activity. Apart from the study to isolate single compound from EA08, a synergistic antibacterial effect between the sub-fraction and beta-lactam antibiotics against MRSA was determined. In order to elucidate the antibacterial restoring mechanism of EA08 on MRSA, mRNA expression of mecA gene and production penicillin-binding protein 2a (PBP2a) encoded by mecA gene were monitored. EA 08 showed the strongest antibacterial activity with MIC value of 256 mu g ml(-1). MIC of oxacillin against MRSA was dramatically reduced from 512 to 16 mu g ml(-1) in combination with 256 mu g ml(-1) of EA08. The fractional inhibitory concentration index of oxacillin was measured at 0.53 in combination with EA08 against MRSA, suggesting that EA08-oxacillin combinations exert synergetic effect against MRSA. The analysis of RT-PCR and Western blotting profiles revealed that EA08 inhibited mRNA expression of mecA gene and production PBP2a, which is a key determinant for beta-lactam antibiotic resistance, in a dose-dependent manner. These results indicated that EA08 eventually led to the reduction or inhibition of PBP2a production through translational inhibition in MRSA.
机译:传统的药用植物含有多种具有有效抗菌活性的化学物质。为了找到解决耐甲氧西林金黄色葡萄球菌(MRSA)问题的替代剂,研究了三叶红叶素对MRSA的抗菌作用。使用最小抑制浓度(MIC)评估三叶假单胞菌甲醇提取物的乙酸乙酯(EtOAc)可溶性提取物的抗菌活性。硅胶开放式柱色谱的EtOAc次级馏分08(EA08)具有很强的抗MRSA活性。除了从EA08中分离单一化合物的研究外,还确定了亚组分和β-内酰胺类抗生素对MRSA的协同抗菌作用。为了阐明EA08对MRSA的抗菌修复机制,监测了mecA基因的mRNA表达以及由mecA基因编码的青霉素结合蛋白2a(PBP2a)的表达。 EA 08表现出最强的抗菌活性,MIC值为256μg ml(-1)。与256μg ml(-1)的EA08结合使用,奥沙西林对MRSA的MIC从512降至16μgml(-1)。与EA08联合使用时,奥沙西林对MRSA的抑制分数浓度分数为0.53,表明EA08-奥沙西林组合对MRSA发挥协同作用。 RT-PCR和蛋白质印迹分析表明,EA08以剂量依赖的方式抑制了mecA基因的mRNA表达和PBP2a的产生,PBP2a是决定β-内酰胺类抗生素耐药性的关键因素。这些结果表明,EA08最终通过MRSA中的翻译抑制作用导致PBP2a产生的减少或抑制。

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