微生物学
噬菌体疗法
感染的多重性
生物
毒力
抗菌剂
体内
鲍曼不动杆菌
噬菌体
细菌
病菌
抗生素耐药性
体外
多粘菌素B
抗生素
溶解循环
病毒学
基因组
多粘菌素
致病菌
噬菌体展示
串行通道
基因
抗药性
DNA
噬菌体分型
人类病原体
最小抑制浓度
不动杆菌
质粒
作者
Yaru Zhi,Dongmei Yan,Qinfang Tang,Lihua Xiao,Aiting Cai,Ming-Zhong Sun,Hongmei Chen,Yungang Wang,Qingping Fu
标识
DOI:10.3389/fmicb.2025.1657539
摘要
Introduction Carbapenem-resistant Acinetobacter baumannii (CRAB) has recently become an important pathogen in clinically acquired infections, making treatment more challenging. Methods The treatment of bacterial infections may improve with the development of phage therapy and phage-antibiotic combination therapy. Here, we reported a novel phage YZ2 that has a double-stranded DNA genome of 40,181 bp with 37.93% GC content. A total of 46 open reading frames (ORFs) and no virulence or antimicrobial resistance genes were annotated in the genome of phage YZ2. Phage YZ2 is a novel member of the Autographiviridae , with a latency period of approximately 20 min and a burst size of approximately 134 phage particles per infected host cell. Results The in vitro antibacterial results demonstrated that YZ2 could rapidly eliminate host bacteria at a low multiplicity of infection, showing strong bactericidal efficacy. In vivo , YZ2 significantly increased the survival rate of A. baumannii -infected Galleria mellonella larvae from 10 to 100% within 72 h. Discussion Moreover, compared with the use of phage or polymyxin B alone, the combined use of phage YZ2 and polymyxin B can significantly increased the survival rate of G. mellonella larvae and had a synergistic effect. These results imply that phage YZ2 has the potential for development as an antimicrobial agent.
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