Mining the Human Gut Microbiota for Immunomodulatory Organisms

被引:588
作者
Geva-Zatorsky, Naama [1 ]
Sefik, Esen [1 ]
Kua, Lindsay [1 ]
Pasman, Lesley [1 ]
Tan, Tze Guan [1 ]
Ortiz-Lopez, Adriana [1 ]
Yanortsang, Tsering Bakto [1 ]
Yang, Liang [1 ]
Jupp, Ray [2 ]
Mathis, Diane [1 ]
Benoist, Christophe [1 ]
Kasper, Dennis L. [1 ]
机构
[1] Harvard Med Sch, Div Immunol, Dept Microbiol & Immunobiol, Boston, MA 02115 USA
[2] UCB Pharma, Slough SL1 3WE, Berks, England
基金
美国国家科学基金会;
关键词
PLASMACYTOID DENDRITIC CELLS; MAINTAIN HOMEOSTASIS; CYTOKINE PRODUCTION; PANETH CELLS; BACTERIA; INNATE; MATURATION; ACCUMULATION; TRAFFICKING; INDUCTION;
D O I
10.1016/j.cell.2017.01.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Within the human gut reside diverse microbes coexisting with the host in a mutually advantageous relationship. Evidence has revealed the pivotal role of the gut microbiota in shaping the immune system. To date, only a few of these microbes have been shown to modulate specific immune parameters. Herein, we broadly identify the immunomodulatory effects of phylogenetically diverse human gut microbes. We monocolonized mice with each of 53 individual bacterial species and systematically analyzed host immunologic adaptation to colonization. Most microbes exerted several specialized, complementary, and redundant transcriptional and immunomodulatory effects. Surprisingly, these were independent of microbial phylogeny. Microbial diversity in the gut ensures robustness of the microbiota's ability to generate a consistent immunomodulatory impact, serving as a highly important epigenetic system. This study provides a foundation for investigation of gut microbiota-host mutualism, highlighting key players that could identify important therapeutics.
引用
收藏
页码:928 / +
页数:27
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