原噬菌体
重叠感染
生物
微生物学
毒力
溶酶原
铜绿假单胞菌
生物膜
细菌
赖氨酸
溶原循环
抗生素耐药性
噬菌体疗法
抗生素
噬菌体
病毒学
遗传学
病毒
大肠杆菌
基因
作者
Michael J. Bucher,Daniel M. Czyż
出处
期刊:Viruses
[MDPI AG]
日期:2024-08-23
卷期号:16 (9): 1348-1348
被引量:2
摘要
Prophages can alter their bacterial hosts to prevent other phages from infecting the same cell, a mechanism known as superinfection exclusion (SIE). Such alterations are facilitated by phage interactions with critical bacterial components involved in motility, adhesion, biofilm production, conjugation, antimicrobial resistance, and immune evasion. Therefore, the impact of SIE extends beyond the immediate defense against superinfection, influencing the overall fitness and virulence of the bacteria. Evaluating the interactions between phages and their bacterial targets is critical for leading phage therapy candidates like Pseudomonas aeruginosa, a Gram-negative bacterium responsible for persistent and antibiotic-resistant opportunistic infections. However, comprehensive literature on the mechanisms underlying SIE remains scarce. Here, we provide a compilation of well-characterized and potential mechanisms employed by Pseudomonas phages to establish SIE. We hypothesize that the fitness costs imposed by SIE affect bacterial virulence, highlighting the potential role of this mechanism in the management of bacterial infections.
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