溶菌性肠球菌噬菌体 vB_Efs8_KEN04 针对肯尼亚耐多药粪肠球菌临床分离株的特性和抗生物膜活性

Viruses Pub Date : 2024-08-09 DOI:10.3390/v16081275
Oumarou Soro, Collins Kigen, A. Nyerere, Moses Gachoya, Martin Georges, Erick Odoyo, L. Musila
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引用次数: 0

摘要

粪肠球菌(Enterococcus faecalis,E. faecalis)是造成医院内感染和耐抗生素感染的一个日益严重的原因。治疗耐药粪肠球菌需要新的方法。使用噬菌体(phages)来对付耐多药(MDR)细菌最近引起了全球关注。生物膜在粪大肠杆菌的致病过程中起着至关重要的作用,因为生物膜会增强抗生素耐药性。噬菌体通过产生溶解酶(包括解聚酶)来消除生物膜。在这项研究中,从肯尼亚内罗毕污水处理厂分离出来的肠球菌噬菌体 vB_Efs8_KEN04 针对 MDR 粪绿球菌的临床菌株进行了测试。该噬菌体对 100%(26/26)的 MDR 粪肠球菌临床分离株具有广泛的宿主范围,对粪肠球菌具有跨物种活性。它能够耐受 pH 值为 3 至 11 的酸性和碱性条件,以及 -80 °C 至 37 °C 的温度。它能抑制和破坏 MDR 粪肠球菌的生物膜。它的线性双链 DNA 基因组长达 142 402 bp,包含 238 个编码序列,G + C 含量和编码基因密度分别为 36.01% 和 91.46%。基因组分析表明,vB_Efs8_KEN04噬菌体属于Herelleviridae科Kochikohdavirus属。它缺乏抗菌素抗性、毒力和裂解基因,其稳定性、广泛的宿主范围和跨物种裂解表明它具有治疗肠球菌感染的强大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization and Anti-Biofilm Activity of Lytic Enterococcus Phage vB_Efs8_KEN04 against Clinical Isolates of Multidrug-Resistant Enterococcus faecalis in Kenya
Enterococcus faecalis (E. faecalis) is a growing cause of nosocomial and antibiotic-resistant infections. Treating drug-resistant E. faecalis requires novel approaches. The use of bacteriophages (phages) against multidrug-resistant (MDR) bacteria has recently garnered global attention. Biofilms play a vital role in E. faecalis pathogenesis as they enhance antibiotic resistance. Phages eliminate biofilms by producing lytic enzymes, including depolymerases. In this study, Enterococcus phage vB_Efs8_KEN04, isolated from a sewage treatment plant in Nairobi, Kenya, was tested against clinical strains of MDR E. faecalis. This phage had a broad host range against 100% (26/26) of MDR E. faecalis clinical isolates and cross-species activity against Enterococcus faecium. It was able to withstand acidic and alkaline conditions, from pH 3 to 11, as well as temperatures between −80 °C and 37 °C. It could inhibit and disrupt the biofilms of MDR E. faecalis. Its linear double-stranded DNA genome of 142,402 bp contains 238 coding sequences with a G + C content and coding gene density of 36.01% and 91.46%, respectively. Genomic analyses showed that phage vB_Efs8_KEN04 belongs to the genus Kochikohdavirus in the family Herelleviridae. It lacked antimicrobial resistance, virulence, and lysogeny genes, and its stability, broad host range, and cross-species lysis indicate strong potential for the treatment of Enterococcus infections.
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