Activities of a broad‐spectrum antimicrobial peptide analogue SAMP‐A4‐C8 and its combat against pneumonia in Staphylococcus aureus‐infected mice

金黄色葡萄球菌 微生物学 白色念珠菌 抗菌剂 白色体 抗生素 耐甲氧西林金黄色葡萄球菌 生物膜 抗菌肽 生物 化学 细菌 遗传学
作者
Ruifang Li,Pu Hao,Kedong Yin,Qingpeng Xu,Shiming Ren,Yingyuan Zhao,Lan Zhang,Beibei Zhang
出处
期刊:Journal of Peptide Science [Wiley]
卷期号:29 (11) 被引量:4
标识
DOI:10.1002/psc.3497
摘要

Antimicrobial peptides and their analogues have become substitutes for antibiotics in recent years. The antimicrobial peptide analogue SAMP‐A4‐C8 ( n ‐octanoic‐VRLLRRRI) with high antimicrobial activity was found in our lab. We speculate that it may kill pathogens by some lethal mechanism of action. In the present investigation, the microbicidal activities of SAMP‐A4‐C8 and its mechanism of action were investigated. The results demonstrated that SAMP‐A4‐C8 had lethal activities against Staphylococcus aureus and Candida albicans by cell disruption. Based on its microbicidal activities, we believe that it is worth further research for its potential as drug candidate. The results showed that SAMP‐A4‐C8, with low propensity to induce the resistance of S. aureus and C. albicans , could kill the persister cells of S. aureus and C. albicans , exhibited biofilm forming inhibition activity and preformed biofilm eradication ability against S. aureus and C. albicans , and displayed therapeutic potential on pneumonia in S. aureus ‐infected mice by reducing lung inflammation. The present study provided a promising drug candidate in the war against multidrug resistance.
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