Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences, 630090 Novosibirsk, Russia.
Viruses. 2024 Feb 29;16(3):385. doi: 10.3390/v16030385.
Bacteria of the genus are significant challenge for medicine, as many species are resistant to multiple antibiotics and some are even to all of the antibiotics we use. One of the approaches to developing new therapeutics to treat staphylococcal infections is the use of bacteriophages specific to these bacteria or the lytic enzymes of such bacteriophages, which are capable of hydrolyzing the cell walls of these bacteria. In this study, a new bacteriophage vB_SepP_134 (St 134) specific to was described. This podophage, with a genome of 18,275 bp, belongs to the genus. St 134 was able to infect various strains of 12 of the 21 tested coagulase-negative species and one clinical strain from the complex. The genes encoding endolysin (LysSte134_1) and tail tip lysin (LysSte134_2) were identified in the St 134 genome. Both enzymes were cloned and produced in cells. The endolysin LysSte134_1 demonstrated catalytic activity against peptidoglycans isolated from , , and . LysSte134_1 was active against and planktonic cells and destroyed the biofilms formed by clinical strains of and .
属细菌是医学的重大挑战,因为许多物种对多种抗生素具有耐药性,有些甚至对我们使用的所有抗生素都具有耐药性。开发治疗葡萄球菌感染的新疗法的一种方法是使用专门针对这些细菌的噬菌体或这些噬菌体的裂解酶,这些酶能够水解这些细菌的细胞壁。在这项研究中,描述了一种新的专门针对 的噬菌体 vB_SepP_134(St 134)。这种 Podophage 的基因组为 18275bp,属于 属。St 134 能够感染 21 种测试的凝固酶阴性葡萄球菌种中的 12 种以及 复合体中的一种临床菌株。St 134 基因组中鉴定出编码内溶素(LysSte134_1)和尾部末端溶素(LysSte134_2)的基因。两种酶均在 细胞中克隆并产生。内溶素 LysSte134_1 对从 、 和 分离的肽聚糖表现出催化活性。LysSte134_1 对 和 浮游细胞具有活性,并破坏 和 临床菌株形成的生物膜。