溶解循环
沙门氏菌
微生物学
肠沙门氏菌
生物
噬菌体疗法
免疫系统
毒力
噬菌体
体内
病毒学
血清型
体外
病毒
细菌
免疫学
大肠杆菌
基因
遗传学
生物技术
生物化学
作者
Lu Liang,Jiaqi Huang,Ketong Cui,Peiyong Li,Wenjian Shi,Fang Lin,Guijuan Hao,Shuhong Sun
标识
DOI:10.3390/ijms232112830
摘要
Effective phage cocktails consisting of multiple virus types are essential for successful phage therapy against pandrug-resistant pathogens, including Salmonella enterica serovar (S.) Typhimurium. Here we show that a Salmonella phage, F118P13, with non-productive infection and a lytic phage, PLL1, combined to inhibit pandrug-resistant S. Typhimurium growth and significantly limited resistance to phages in vitro. Further, intraperitoneal injection with this unique phage combination completely protected mice from Salmonella-induced death and inhibited bacterial proliferation rapidly in various organs. Furthermore, the phage combination treatment significantly attenuated the inflammatory response, restored the generation of CD4+ T cells repressed by Salmonella, and allowed macrophages and granulocytes to participate in immunophage synergy to promote bacterial clearance. Crucially, the non-productive phage F118P13 is less likely to be cleared by the immune system in vivo, thus providing an alternative to phage cocktail against bacterial infections.
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