生物
溶解循环
微生物学
噬菌体疗法
噬菌体
粪肠球菌
屎肠球菌
抗生素耐药性
细菌
基因组
噬菌体分型
噬菌体展示
计算生物学
病毒学
抗生素
遗传学
金黄色葡萄球菌
基因
血清型
大肠杆菌
病毒
抗体
作者
Alhassan Alrafaie,Karolina Pyrzanowska,Elspeth M. Smith,David G. Partridge,John Rafferty,Stéphane Mesnage,Joanna Shepherd,Graham P. Stafford
出处
期刊:Virus Research
[Elsevier BV]
日期:2024-07-04
卷期号:347: 199426-199426
被引量:4
标识
DOI:10.1016/j.virusres.2024.199426
摘要
Enterococci are robust Gram-positive bacteria that pose a significant threat in healthcare settings due to antibiotic resistance, with vancomycin-resistant enterococci (VRE) most prominent. To tackle this issue, bacteriophages (bacterial viruses) can be exploited as they specifically and efficiently target bacteria. Here, we successfully isolated and characterised a set of novel phages: SHEF10, SHEF11, SHEF13, SHEF14, and SHEF16 which target E. faecalis (SHEF10,11,13), or E. faecium (SHEF13, SHEF14 & SHEF16) strains including a range of clinical and VRE isolates. Genomic analysis shows that all phages are strictly lytic and diverse in terms of genome size and content, quickly and effectively lysing strains at different multiplicity of infections. Detailed analysis of the broad host-range SHEF13 phage revealed the crucial role of the enterococcal polysaccharide antigen (EPA) variable region in its infection of E. faecalis V583. In parallel, the discovery of a carbohydrate-targeting domain (CBM22) found conserved within the three phage genomes indicates a role in cell surface interactions that may be important in phage-bacterial interactons. These findings advance our comprehension of phage-host interactions and pave the way for targeted therapeutic strategies against antibiotic-resistant enterococcal infections.
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