铜绿假单胞菌
囊性纤维化
抗生素
微生物学
抗菌剂
抗生素耐药性
体内
多重耐药
医学
生物
细菌
生物技术
内科学
遗传学
作者
Abdulaziz Alqahtani,Jonathan Kopel,Abdul N. Hamood
出处
期刊:Antibiotics
[Multidisciplinary Digital Publishing Institute]
日期:2022-10-07
卷期号:11 (10): 1366-1366
被引量:7
标识
DOI:10.3390/antibiotics11101366
摘要
Pseudomonas aeruginosa can cause several life-threatening infections among immunocompromised patients (e.g., cystic fibrosis) due to its ability to adapt and develop resistance to several antibiotics. In recent years, P. aeruginosa infections has become difficult to treat using conventional antibiotics due to the increase multidrug-resistant P. aeruginosa strains. Therefore, there is a growing interest to develop novel treatments against antibiotic-resistance P. aeruginosa strains. One novel method includes the application of antimicrobial peptides secreted by P. aeruginosa strains, known as pyocins. In this review, we will discuss the structure, function, and use of pyocins in the pathogenesis and treatment of P. aeruginosa infection.
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