State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, 430072, People's Republic of China.
Appl Microbiol Biotechnol. 2016 Jun;100(11):5069-77. doi: 10.1007/s00253-016-7395-x. Epub 2016 Mar 8.
As an alternative class of antimicrobial agents used to overcome drug-resistant infections, antimicrobial peptides (AMPs) have recently gained significant attention. In this study, we designed an improved antimicrobial peptide, K1K8, based on the molecular template of Hp1404. Compared to the wild-type Hp1404, K1K8 showed an improved antibacterial spectrum in vitro, a lower hemolytic activity, and an enhanced serum stability. Importantly, K1K8 also decreased methicillin-resistant Staphylococcus aureus (MRSA) bacterial counts in the wounded region in a mouse skin infection model. Interestingly, K1K8 did not induce bacterial resistance or non-specific immune response reactions. Moreover, the peptide killed bacterial cells mainly by disrupting the bacterial membrane. In summary, K1K8 has the potential to be used as an improved anti-infection agent for topical use, which opens an avenue that potential anti-infection drugs may be designed and developed from the molecular templates of AMPs.
作为一种用于克服耐药性感染的替代类抗菌药物,抗菌肽(AMPs)最近受到了广泛关注。在这项研究中,我们基于 Hp1404 的分子模板设计了一种改良的抗菌肽 K1K8。与野生型 Hp1404 相比,K1K8 在体外显示出了改善的抗菌谱、更低的溶血活性和增强的血清稳定性。重要的是,K1K8 还能降低小鼠皮肤感染模型中创伤部位耐甲氧西林金黄色葡萄球菌(MRSA)的细菌计数。有趣的是,K1K8 不会诱导细菌产生耐药性或非特异性免疫反应。此外,该肽主要通过破坏细菌膜来杀死细菌细胞。总之,K1K8 有可能被用作局部抗感染的改良剂,这为可能的抗感染药物的设计和开发提供了一种途径,这些药物可以从 AMPs 的分子模板中获得。