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Macropis fulvipes Venom component Macropin Exerts its Antibacterial and Anti-Biofilm Properties by Damaging the Plasma Membranes of Drug Resistant Bacteria

机译:猴小毒蛇毒成分Macropin通过破坏耐药细菌的血浆膜来发挥其抗菌和抗生物膜特性

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摘要

The abuse of antibiotics for disease treatment has led to the emergence of multidrug resistant bacteria. Antimicrobial peptides, found naturally in various organisms, have received increasing interest as alternatives to conventional antibiotics because of their broad spectrum antimicrobial activity and low cytotoxicity. In a previous report, Macropin, isolated from bee venom, exhibited antimicrobial activity against both gram-positive and negative bacteria. In the present study, Macropin was synthesized and its antibacterial and anti-biofilm activities were tested against bacterial strains, including gram-positive and negative bacteria, and drug resistant bacteria. Moreover, Macropin did not exhibit hemolytic activity and cytotoxicity to keratinocytes, whereas Melittin, as a positive control, showed very high toxicity. Circular dichroism assays showed that Macropin has an α-helical structure in membrane mimic environments. Macropin binds to peptidoglycan and lipopolysaccharide and kills the bacteria by disrupting their membranes. Moreover, the fractional inhibitory concentration index indicated that Macropin has additive and partially synergistic effects with conventional antibiotics against drug resistant bacteria. Thus, our study suggested that Macropin has potential for use of an antimicrobial agent for infectious bacteria, including drug resistant bacteria.
机译:抗生素在疾病治疗中的滥用导致了多药耐药细菌的出现。天然存在于各种生物中的抗菌肽由于其广谱抗菌活性和低细胞毒性而作为常规抗生素的替代品受到越来越多的关注。在以前的报告中,从蜂毒中分离出的Macropin对革兰氏阳性和阴性细菌均表现出抗菌活性。在本研究中,Macropin是合成的,并且针对细菌菌株(包括革兰氏阳性和阴性细菌以及耐药菌)测试了其抗菌和抗生物膜活性。此外,Macropin对角质形成细胞没有溶血活性和细胞毒性,而作为阳性对照的蜂毒肽则显示出很高的毒性。圆二色性分析表明,Macropin在膜模拟环境中具有α螺旋结构。 Macropin与肽聚糖和脂多糖结合,并通过破坏其膜杀死细菌。此外,分数抑制浓度指数表明Macropin与常规抗生素具有抗药性细菌的累加和部分协同作用。因此,我们的研究表明,Macropin具有用于抗菌药物(包括抗药性细菌)的抗菌剂的潜力。

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