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一种新型抗菌肽 S24 可对抗由铜绿假单胞菌和鲍曼不动杆菌引起的严重伤口感染。

A novel antimicrobial peptide S24 combats serious wound infections caused by Pseudomonas aeruginosa and Acinetobacter baumannii.

机构信息

School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University, Shenyang 110016, China.

Weihuakang (Shenzhen) Biotech. Co., Ltd., Shenzhen 518001, China.

出版信息

J Antimicrob Chemother. 2024 Aug 1;79(8):1951-1961. doi: 10.1093/jac/dkae191.

Abstract

OBJECTIVES

Pseudomonas aeruginosa and Acinetobacter baumannii are ranked as top-priority organisms by WHO. Antimicrobial peptides (AMPs) are promising antimicrobial agents that are highly effective against serious bacterial infections.

METHODS

In our previous study, a series of α-helical AMPs were screened using a novel multiple-descriptor strategy. The current research suggested that S24 exhibited strong antimicrobial activity against major pathogenic bacteria, and displayed minimal haemolysis, good serum stability and maintained salt resistance.

RESULTS

We found that S24 exerted an antimicrobial effect by destroying outer membrane permeability and producing a strong binding effect on bacterial genomic DNA that inhibits genomic DNA migration. Furthermore, S24 exerted a strong ability to promote healing in wound infected by P. aeruginosa, A. baumannii and mixed strains in a mouse model.

CONCLUSIONS

Overall, S24 showed good stability under physiological conditions and excellent antimicrobial activity, suggesting it may be a potential candidate for the development of serious bacterial infection treatment.

摘要

目的

铜绿假单胞菌和鲍曼不动杆菌被世界卫生组织列为优先考虑的病原体。抗菌肽(AMPs)是一种很有前途的抗菌药物,对严重的细菌感染非常有效。

方法

在我们之前的研究中,使用一种新的多描述符策略筛选了一系列α-螺旋抗菌肽。目前的研究表明,S24 对主要致病菌表现出很强的抗菌活性,且溶血作用最小,血清稳定性好,保持耐盐性。

结果

我们发现 S24 通过破坏外膜通透性并对细菌基因组 DNA 产生强烈的结合作用来抑制基因组 DNA 迁移,从而发挥抗菌作用。此外,S24 在小鼠模型中对铜绿假单胞菌、鲍曼不动杆菌和混合菌株感染的伤口表现出很强的愈合促进作用。

结论

总的来说,S24 在生理条件下表现出良好的稳定性和优异的抗菌活性,表明它可能是治疗严重细菌感染的潜在候选药物。

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