效应器
先天免疫系统
免疫系统
HEK 293细胞
生物
细胞生物学
细胞外小泡
细菌
分泌物
肽聚糖
益生菌
细胞外
微生物学
生物化学
基因
免疫学
遗传学
作者
Yilan Liu,jinjin chen,Kaushik Raj,Lauren Baerg,Nayanan Nathan,Dana J. Philpott,Radhakrishnan Mahadevan
标识
DOI:10.1021/acssynbio.2c00583
摘要
Both Gram-positive and Gram-negative bacteria release nanosized extracellular vesicles called membrane vesicles (MVs, 20-400 nm), which have great potential in various biomedical applications due to their abilities to deliver effector molecules and induce therapeutic responses. To fully utilize bacterial MVs for therapeutic purposes, regulated and enhanced production of MVs would be highly advantageous. In this study, we developed a universal method to enhance MV yields in both G+/G- bacteria through an autonomous controlled peptidoglycan hydrolase (PGase) expression system. A significant increase (9.37-fold) of MV concentration was observed in engineered E. coli Nissle 1917 compared to the wild-type. With the help of this autonomous system, for the first time we experimentally confirmed horizontal gene transfer and nutrient acquisition in a cocultured bacterial consortium. Furthermore, the engineered probiotic E. coli strains with high yield of MVs showed higher activation of the innate immune responses in human embryonic kidney 293T (HEK293T) and human colorectal carcinoma cells (HCT116), thereby demonstrating the great potential of engineering probiotics in immunology and further living therapeutics in humans.
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