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

被引:5
|
作者
Li, Ruifang [1 ,2 ,4 ]
Hao, Pu [1 ,2 ]
Yin, Kedong [3 ]
Xu, Qingpeng [3 ]
Ren, Shiming [1 ]
Zhao, Yingyuan [1 ,2 ]
Zhang, Lan [1 ,2 ]
Zhang, Beibei [1 ,2 ,4 ]
机构
[1] Henan Univ Technol, Coll Biol Engn, Zhengzhou, Peoples R China
[2] Key Lab Funct Mol Biomed Res, Zhengzhou, Peoples R China
[3] Henan Univ Technol, Coll Informat Sci & Engn, Zhengzhou, Peoples R China
[4] Henan Univ Technol, Coll Biol Engn, 100 Lianhua St, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
antimicrobial peptides; biofilm forming inhibition; drug resistance; microbicidal activity; persister cells; preformed biofilm eradication; S; aureus pneumonia;
D O I
10.1002/psc.3497
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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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页数:11
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