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Antimicrobial Enzyme Fusions Reduce Resistance and Kill Intracellular Staphylococcus aureus

机译:抗菌酶融合物降低耐药性并杀死细胞内金黄色葡萄球菌

摘要

Multi-drug resistant bacteria are a persistent problem in modern health care, food safety and animal health. There is a need for new antimicrobials to replace over-used conventional antibiotics. Here we describe engineered triple-acting staphylolytic peptidoglycan hydrolases wherein three unique antimicrobial activities from two parental proteins are combined into a single fusion protein, effectively reducing the incidence of resistant strain development. The fusion protein reduced colonization by S. aureus in a rat nasal colonization model, surpassing the efficacy of either parental protein. Modification of the triple-acting lytic construct with a protein transduction domain significantly enhanced both biofilm eradication and the ability to kill intracellular Staphylococcus aureus as demonstrated in cultured cells, and mouse models of staphylococcal mastitis and osteomyelitis. Bacterial cell wall degrading enzyme antimicrobials can be engineered to enhance their value as potent therapeutics.
机译:在现代卫生保健,食品安全和动物健康中,耐多药细菌是一个持续存在的问题。需要新的抗生素来代替过度使用的常规抗生素。在这里,我们描述了工程化的三作用葡萄球菌肽聚糖水解酶,其中来自两个亲本蛋白的三个独特的抗菌活性被组合到一个融合蛋白中,有效地降低了耐药菌株的发生率。融合蛋白通过I减少了定植。金黄色葡萄球菌在大鼠鼻内定植模型中的功效超过了任何一种亲本蛋白的功效。如在培养的细胞以及葡萄球菌性乳腺炎和骨髓炎的小鼠模型中所示,用蛋白质转导域修饰三重作用的裂解构建体可显着增强生物膜的清除和杀死细胞内金黄色葡萄球菌的能力。可以对细菌细胞壁降解酶抗菌素进行改造,以增强其作为有效治疗剂的价值。

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