殖民地化
细菌
大肠杆菌
重组DNA
生物
寄主(生物学)
微生物学
细胞生物学
生物化学
生态学
遗传学
基因
作者
Meihui Cui,Tao Sun,Shubin Li,Huizhuo Pan,Jing Liu,Xinyu Zhang,Lianyue Li,Shanshan Li,Chunyang Wei,Chengzhuang Yu,Chun Yang,Ning Ma,Binglin Ma,Shenjunjie Lu,Jin Chang,Weiwen Zhang,Hanjie Wang
出处
期刊:Cell Reports
[Elsevier]
日期:2021-09-01
卷期号:36 (11): 109690-109690
被引量:25
标识
DOI:10.1016/j.celrep.2021.109690
摘要
Recombinant bacterial colonization plays an indispensable role in disease prevention, alleviation, and treatment. Successful application mainly depends on whether bacteria can efficiently spatiotemporally colonize the host gut. However, a primary limitation of existing methods is the lack of precise spatiotemporal regulation, resulting in uncontrolled methods that are less effective. Herein, we design upconversion microgels (UCMs) to convert near-infrared light (NIR) into blue light to activate recombinant light-responsive bacteria (Lresb) in vivo, where autocrine "functional cellular glues" made of adhesive proteins assist Lresb inefficiently colonizing the gut. The programmable engineering platform is further developed for the controlled and effective colonization of Escherichia coli Nissle 1917 (EcN) in the gut. The colonizing bacteria effectively alleviate DSS-induced colitis in mice. We anticipate that this approach could facilitate the clinical application of engineered microbial therapeutics to accurately and effectively regulate host health.
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