Department of Medical Laboratory, College of Applied Medical Sciences in Al-Kharj, Prince Sattam Bin Abdulaziz University, Al-Kharj 11942, Saudi Arabia.
School of Clinical Dentistry, University of Sheffield, Sheffield, United Kingdom, S10 2TA, UK.
Virus Res. 2024 Sep;347:199426. doi: 10.1016/j.virusres.2024.199426. Epub 2024 Jul 4.
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.
肠球菌是一种强壮的革兰氏阳性细菌,由于抗生素耐药性,它们在医疗保健环境中构成了重大威胁,其中耐万古霉素肠球菌(VRE)最为突出。为了解决这个问题,可以利用噬菌体(细菌病毒),因为它们可以特异性和有效地靶向细菌。在这里,我们成功地分离和表征了一组新型噬菌体:SHEF10、SHEF11、SHEF13、SHEF14 和 SHEF16,它们针对粪肠球菌(SHEF10、11、13)或屎肠球菌(SHEF13、SHEF14 和 SHEF16)菌株,包括一系列临床和 VRE 分离株。基因组分析表明,所有噬菌体都是严格的裂解性的,在基因组大小和内容方面具有多样性,能够在不同的感染复数下快速有效地裂解菌株。对广谱宿主 SHEF13 噬菌体的详细分析表明,肠球菌多糖抗原(EPA)可变区在其感染粪肠球菌 V583 中的关键作用。同时,在三个噬菌体基因组中发现的碳水化合物靶向结构域(CBM22)表明其在细胞表面相互作用中发挥作用,这可能在噬菌体-细菌相互作用中很重要。这些发现提高了我们对噬菌体-宿主相互作用的理解,并为针对抗生素耐药性肠球菌感染的靶向治疗策略铺平了道路。