微生物学
支原体
结核分枝杆菌
溶解循环
分枝杆菌
生物
病毒学
细胞内寄生虫
肺结核
噬菌体疗法
免疫系统
细菌
噬菌体
免疫学
病毒
医学
生物化学
遗传学
病理
大肠杆菌
基因
作者
Lawrence Broxmeyer,Danuta Sosnowska,Elizabeth Miltner,Ofelia Chacón,Dirk Wagner,Jeffery A. McGarvey,Raúl G. Barletta,Luiz E. Bermudez
摘要
Mycobacterium avium causes disseminated infection in patients with acquired immune deficieny syndrome. Mycobacterium tuberculosis is a pathogen associated with the deaths of millions of people worldwide annually. Effective therapeutic regimens exist that are limited by the emergence of drug resistance and the inability of antibiotics to kill dormant organisms. The present study describes a system using Mycobacterium smegmatis an avirulent mycobacterium, to deliver the lytic phage TM4 where both M. avium and M. tuberculosis reside within macrophages. These results showed that treatment of M. avium–infected, as well as M. tuberculosis–infected, RAW 264.7 macrophages, with M. smegmatis transiently infected with TM4, resulted in a significant time- and titer-dependent reduction in the number of viable intracellular bacilli. In addition, the M. smegmatis vacuole harboring TM4 fuses with the M. avium vacuole in macrophages. These results suggest a potentially novel concept to kill intracellular pathogenic bacteria and warrant future development
科研通智能强力驱动
Strongly Powered by AbleSci AI