School of Biological Sciences, Monash University, Clayton, Victoria, Australia.
Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, Victoria, Australia.
Nat Microbiol. 2021 Feb;6(2):157-161. doi: 10.1038/s41564-020-00830-7. Epub 2021 Jan 11.
We characterized two bacteriophages, ΦFG02 and ΦCO01, against clinical isolates of Acinetobacter baumannii and established that the bacterial capsule is the receptor for these phages. Phage-resistant mutants harboured loss-of-function mutations in genes responsible for capsule biosynthesis, resulting in capsule loss and disruption of phage adsorption. The phage-resistant strains were resensitized to human complement, beta-lactam antibiotics and alternative phages and exhibited diminished fitness in vivo. Using a mouse model of A. baumannii infection, we showed that phage therapy was effective.
我们对两种针对鲍曼不动杆菌临床分离株的噬菌体(ΦFG02 和 ΦCO01)进行了特性分析,结果表明细菌荚膜是这些噬菌体的受体。噬菌体抗性突变株在负责荚膜生物合成的基因中存在功能丧失突变,导致荚膜丢失和噬菌体吸附中断。这些噬菌体抗性菌株对人补体、β-内酰胺类抗生素和替代噬菌体重新敏感,并在体内表现出降低的适应性。使用鲍曼不动杆菌感染的小鼠模型,我们表明噬菌体治疗是有效的。