细菌素
金黄色葡萄球菌
抗菌剂
微生物学
抗菌肽
抗生素
生物
细菌
抗生素耐药性
生物膜
病菌
遗传学
作者
Logan L. Newstead,Katarina Varjonen,Tim Nuttall,Gavin K. Paterson
出处
期刊:Antibiotics
[MDPI AG]
日期:2020-01-21
卷期号:9 (2): 40-40
被引量:67
标识
DOI:10.3390/antibiotics9020040
摘要
Staphylococcus aureus is an important pathogen of both humans and animals, implicated in a wide range of infections. The emergence of antibiotic resistance has resulted in S. aureus strains that are resistant to almost all available antibiotics, making treatment a clinical challenge. Development of novel antimicrobial approaches is now a priority worldwide. Bacteria produce a range of antimicrobial peptides; the most diverse of these being bacteriocins. Bacteriocins are ribosomally synthesised peptides, displaying potent antimicrobial activity usually against bacteria phylogenetically related to the producer strain. Several bacteriocins have been isolated from commensal coagulase-negative staphylococci, many of which display inhibitory activity against S. aureus in vitro and in vivo. The ability of these bacteriocins to target biofilm formation and their novel mechanisms of action with efficacy against antibiotic-resistant bacteria make them strong candidates as novel therapeutic antimicrobials. The use of genome-mining tools will help to advance identification and classification of bacteriocins. This review discusses the staphylococcal-derived antimicrobial peptides displaying promise as novel treatments for S. aureus infections.
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