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抗耐甲氧西林金黄色葡萄球菌抗菌肽的研究进展

王昱璇 郭伟昌 陈诚 罗瑶 肖亚雄 李江涛

中国药房2025,Vol.36Issue(5):636-640,5.
中国药房2025,Vol.36Issue(5):636-640,5.DOI:10.6039/j.issn.1001-0408.2025.05.23

抗耐甲氧西林金黄色葡萄球菌抗菌肽的研究进展

Research progress on antimicrobial peptides against methicillin-resistant Staphylococcus aureus

王昱璇 1郭伟昌 2陈诚 3罗瑶 1肖亚雄 4李江涛5

作者信息

  • 1. 宜宾市第一人民医院医务科,四川宜宾 644000
  • 2. 宜宾市第一人民医院血管外科,四川宜宾 644000
  • 3. 宜宾市第一人民医院药学部,四川宜宾 644000
  • 4. 宜宾市第一人民医院中心实验室,四川宜宾 644000
  • 5. 宜宾市第一人民医院风湿免疫科,四川宜宾 644000
  • 折叠

摘要

Abstract

Staphylococcus aureus is a Gram-positive bacterium with strong pathogenicity.With the widespread use of antibiotics,its multi-drug resistance has gradually increased.Among them,methicillin-resistant S.aureus(MRSA)is one of the main pathogens of hospital and community infections.Antimicrobial peptides are short-chain peptides with good antibacterial effects and low drug resistance,which have been widely studied in recent years.This study summarizes the mechanism of action of antimicrobial peptides and related study on antimicrobial peptides against MRSA from different sources.It is found that the mechanisms of action of antimicrobial peptides include targeting bacterial cell membranes,bacterial cells,and bacterial cell walls,etc.Besides isolating antimicrobial peptides with anti-MRSA activity from animals,plants,and microorganisms,antimicrobial peptides can also be obtained through synthetic methods.Among them,GHa-derived peptides from animal sources,Ib-AMP4 from plant sources,Ph-SA from microbial sources,the synthetic peptide LLKLLLKLL-NH2,and so on,due to their effective antibacterial activity,rapid bactericidal speed,and low toxicity,are promising candidates for anti-MRSA drugs.

关键词

耐甲氧西林金黄色葡萄球菌/抗菌肽/作用机制/耐药性

Key words

methicillin-resistant Staphylococcus aureus/antimicrobial peptides/mechanism of action/drug resistance

分类

医药卫生

引用本文复制引用

王昱璇,郭伟昌,陈诚,罗瑶,肖亚雄,李江涛..抗耐甲氧西林金黄色葡萄球菌抗菌肽的研究进展[J].中国药房,2025,36(5):636-640,5.

基金项目

四川省医学科研课题(No.S23039) (No.S23039)

中国药房

OA北大核心

1001-0408

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