From germ-free to wild: modulating microbiome complexity to understand mucosal immunology

被引:19
作者
Thomson, Carolyn A. [1 ]
Morgan, Sydney C. [1 ,2 ]
Ohland, Christina [2 ]
McCoy, Kathy D. [1 ,2 ]
机构
[1] Univ Calgary, Cumming Sch Med, Snyder Inst Chron Dis, Dept Physiol & Pharmacol, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Int Microbiome Ctr, Cumming Sch Med, Calgary, AB T2N 4N1, Canada
基金
加拿大健康研究院;
关键词
REGULATORY T-CELLS; SEGMENTED FILAMENTOUS BACTERIA; NATURAL-KILLER-CELLS; HUMAN GUT MICROBIOTA; EARLY-LIFE; DIABETES DEVELOPMENT; LUNG MICROBIOTA; CYTOKINE STORM; TH17; CELLS; IMMUNE;
D O I
10.1038/s41385-022-00562-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gut microbiota influences host responses at practically every level, and as research into host-microbe interactions expands, it is not surprising that we are uncovering similar roles for the microbiota at other barrier sites, such as the lung and skin. Using standard laboratory mice to assess host-microbe interactions, or even host intrinsic responses, can be challenging, as slight variations in the microbiota can affect experimental outcomes. When it comes to designing and selecting an appropriate level of microbial diversity and community structure for colonization of our laboratory rodents, we have more choices available to us than ever before. Here we will discuss the different approaches used to modulate microbial complexity that are available to study host-microbe interactions. We will describe how different models have been used to answer distinct biological questions, covering the entire microbial spectrum, from germ-free to wild.
引用
收藏
页码:1085 / 1094
页数:10
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