Intestinal microbiome adjusts the innate immune setpoint during colonization through negative regulation of MyD88.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30291253.
- Also identified by DOI 10.1038/s41467-018-06658-4 and PMC identifier 6173721.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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.
Medical subject headings
- Gastrointestinal Microbiome
- Immunity, Innate
- Intestinal Mucosa
- Myeloid Differentiation Factor 88
- Zebrafish Proteins