Institute of Biology, Leiden University, 2333 BE, Leiden, The Netherlands.
Department of Molecular Biology and Genetics, Aarhus University, 8000, Aarhus C, Denmark.
Nat Commun. 2018 Oct 5;9(1):4099. doi: 10.1038/s41467-018-06658-4.
Host pathways mediating changes in immune states elicited by intestinal microbial colonization are incompletely characterized. Here we describe alterations of the host immune state induced by colonization of germ-free zebrafish larvae with an intestinal microbial community or single bacterial species. We show that microbiota-induced changes in intestinal leukocyte subsets and whole-body host gene expression are dependent on the innate immune adaptor gene myd88. Similar patterns of gene expression are elicited by colonization with conventional microbiome, as well as mono-colonization with two different zebrafish commensal bacterial strains. By studying loss-of-function myd88 mutants, we find that colonization suppresses Myd88 at the mRNA level. Tlr2 is essential for microbiota-induced effects on myd88 transcription and intestinal immune cell composition.
宿主途径介导肠道微生物定植引起的免疫状态变化尚未完全阐明。在这里,我们描述了无菌斑马鱼幼虫定植肠道微生物群落或单一细菌物种引起的宿主免疫状态的改变。我们表明,微生物群诱导的肠道白细胞亚群和全身宿主基因表达的变化依赖于先天免疫接头基因 myd88。用常规微生物组定植以及用两种不同的斑马鱼共生细菌单定植也会引发类似的基因表达模式。通过研究功能丧失的 myd88 突变体,我们发现定植在 mRNA 水平上抑制了 Myd88。Tlr2 对于微生物群诱导的 myd88 转录和肠道免疫细胞组成的影响是必不可少的。