Biological function identification of phage holin Hol-4086 and treatment of Staphylococcus aureus infection

金黄色葡萄球菌 微生物学 生物 鉴定(生物学) 遗传学 细菌 生态学
作者
Zheng Chang,Y. Peter Di,Yingchun Wang,Hongmei Zhao,Ruichong Wang,Guiwei Li,Xiaona Wang,Zhifu San,Yanping Jiang,Wen Cui,Jiaxuan Li,Li Wang,Xinyuan Qiao
出处
期刊:Frontiers in Microbiology [Frontiers Media]
卷期号:16: 1499566-1499566 被引量:4
标识
DOI:10.3389/fmicb.2025.1499566
摘要

The treatment of infections caused by drug-resistant Staphylococcus aureus has become increasingly difficult. In this study, the complete genome of phage 4086-1 against S. aureus was sequenced and shown to be 17,960 bp in size, with a GC content of 29.14%. Phylogenetic analysis demonstrated that phage 4086-1 exhibited a close relationship with the Staphylococcus phages SLPW, JPL-50, and LSA2366. BLAST analysis indicated that ORF12 of phage 4086-1 (termed Hol-4086) shares high identity with other reported phage-associated holins. Hol-4086 consists of 140 amino acids and exhibits high sequence identity with some members of the phage_holin_4_1 superfamily (18–125 amino acids). Hol-4086 was then expressed in Escherichia coli and detected using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and western blotting. The results of a spot test demonstrated that Hol-4086 had substantial bacteriostatic effects on the host bacteria. S. aureus cells were exposed to Hol-4086 and observed using transmission electron microscopy and scanning electron microscopy. Bacterial cells treated with Hol-4086 showed ultrastructural and morphological changes. The detection of biofilm activity showed that Hol-4086 effectively inhibited and removed S. aureus biofilms. In vivo , treatment with Hol-4086 significantly reduced the number of bacteria, relieved inflammatory responses, and alleviated pathological changes in the organs of infected mice 48 h after treatment. These results demonstrate that Hol-4086 exhibits promising antibacterial potential as an alternative therapy for the treatment of infections caused by S. aureus .
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