A Universal Strategy to Promote Secretion of G plus /G- Bacterial Extracellular Vesicles and Its Application in Host Innate Immune Responses

被引:12
|
作者
Liu, Yilan [1 ]
Chen, Jinjin [1 ]
Raj, Kaushik [1 ]
Baerg, Lauren [2 ]
Nathan, Nayanan [3 ]
Philpott, Dana J. [3 ]
Mahadevan, Radhakrishnan [1 ,2 ]
机构
[1] Univ Toronto, Dept Chem Engn & Appl Chem, Toronto, ON M5S 3E5, Canada
[2] Univ Toronto, Inst Biomed Engn, Toronto, ON M5S 3G9, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
来源
ACS SYNTHETIC BIOLOGY | 2023年 / 12卷 / 01期
关键词
engineer; peptidoglycan hydrolase; membrane vesicles; bacterial communication; immune response; OUTER-MEMBRANE VESICLES; ESCHERICHIA-COLI; GENE-TRANSFER; PEPTIDOGLYCAN; ANTIGEN; VACCINE; STRESS; SENSOR; CELLS; NOD2;
D O I
10.1021/acssynbio.2c00583
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:319 / 328
页数:10
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