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Intestinal microbiome adjusts the innate immune setpoint during colonization through negative regulation of MyD88

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  • Bjørn E. V. Koch

    (Leiden University
    Aarhus University)

  • Shuxin Yang

    (Leiden University
    Chinese Academy of Sciences)

  • Gerda Lamers

    (Leiden University)

  • Jens Stougaard

    (Aarhus University)

  • Herman P. Spaink

    (Leiden University)

Abstract

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.

Suggested Citation

  • Bjørn E. V. Koch & Shuxin Yang & Gerda Lamers & Jens Stougaard & Herman P. Spaink, 2018. "Intestinal microbiome adjusts the innate immune setpoint during colonization through negative regulation of MyD88," Nature Communications, Nature, vol. 9(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-06658-4
    DOI: 10.1038/s41467-018-06658-4
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