Department of Microbiology, School of Medicine, Kyungpook National University, Daegu 41944, Korea.
Viruses. 2020 Nov 23;12(11):1340. doi: 10.3390/v12111340.
Multidrug-resistant (MDR) bacteria are a major threat to public health. Bacteriophage endolysins (lysins) are a promising alternative treatment to traditional antibiotics. However, the lysins currently under development are still underestimated. Herein, we cloned the lysin from the SAP-26 bacteriophage genome. The recombinant LysSAP26 protein inhibited the growth of carbapenem-resistant , , , and , oxacillin-resistant , and vancomycin-resistant with minimum inhibitory concentrations of 5~80 µg/mL. In animal experiments, mice infected with were protected by LysSAP26, with a 40% survival rate. Transmission electron microscopy analysis confirmed that LysSAP26 treatment resulted in the destruction of bacterial cell walls. LysSAP26 is a new endolysin that can be applied to treat MDR , , , , , and infections, targeting both Gram-positive and Gram-negative bacteria.
耐多药(MDR)细菌对公共健康构成重大威胁。噬菌体裂解酶(lysins)是一种有前途的传统抗生素替代治疗方法。然而,目前正在开发的裂解酶仍被低估。在此,我们从 SAP-26 噬菌体基因组中克隆了裂解酶。重组 LysSAP26 蛋白抑制了耐碳青霉烯、耐、耐、耐 和耐 、耐 和耐万古霉素的生长,最小抑菌浓度为 5~80µg/mL。在动物实验中,用 LysSAP26 处理可保护感染 的小鼠,存活率为 40%。透射电子显微镜分析证实,LysSAP26 处理导致细菌细胞壁的破坏。LysSAP26 是一种新的裂解酶,可用于治疗 MDR 、 、 、 、 、 和 感染,针对革兰氏阳性和革兰氏阴性细菌。