A diverse set of Enterococcus-infecting phage provides insight into phage host-range determinants

IF 2.5 4区 医学 Q3 VIROLOGY Virus research Pub Date : 2024-07-04 DOI:10.1016/j.virusres.2024.199426
Alhassan M. Alrafaie , Karolina Pyrzanowska , Elspeth M. Smith , David G. Partridge , John Rafferty , Stephane Mesnage , Joanna Shepherd , Graham P. Stafford
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Abstract

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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通过一组不同的肠球菌感染噬菌体,可以深入了解噬菌体的宿主范围决定因素。
肠球菌是一种强健的革兰氏阳性细菌,由于具有抗生素耐药性,对医疗机构构成了严重威胁,其中耐万古霉素肠球菌(VRE)最为突出。要解决这一问题,可以利用噬菌体(细菌病毒),因为它们能特异、高效地靶向细菌。在这里,我们成功分离并鉴定了一组新型噬菌体:SHEF10、SHEF11、SHEF13、SHEF14 和 SHEF16,这些噬菌体靶向粪肠球菌(SHEF10、11、13)或粪肠球菌(SHEF13、SHEF14 和 SHEF16)菌株,包括一系列临床和疱疹病毒分离株。基因组分析表明,所有噬菌体都具有严格的溶菌能力,而且基因组大小和含量各不相同,能快速有效地裂解不同感染倍数的菌株。对宿主范围广泛的 SHEF13 噬菌体的详细分析显示,肠球菌多糖抗原(EPA)可变区在其感染粪肠球菌 V583 的过程中发挥了关键作用。与此同时,在三种噬菌体基因组中发现的一个碳水化合物靶向结构域(CBM22)表明,噬菌体在细胞表面相互作用中可能扮演着重要角色。这些发现加深了我们对噬菌体-宿主相互作用的理解,并为针对抗生素耐药肠球菌感染的靶向治疗策略铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virus research
Virus research 医学-病毒学
CiteScore
9.50
自引率
2.00%
发文量
239
审稿时长
43 days
期刊介绍: Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.
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