Linking genetic variation in human Toll-like receptor 5 genes to the gut microbiome's potential to cause inflammation

Immunol Lett. 2014 Dec;162(2 Pt A):3-9. doi: 10.1016/j.imlet.2014.07.017. Epub 2014 Oct 2.

Abstract

Immunodeficiencies can lead to alterations of the gut microbiome that render it pathogenic and capable of transmitting disease to naïve hosts. Here, we review the role of Toll-like receptor (TLR) 5, the innate receptor for bacterial flagellin, in immune responses to the normal gut microbiota with a focus its role on adaptive immunity. Loss of TLR5 has profound effects on the microbiota that include greater temporal instability of major lineages and upregulation of flagellar motility genes that may be linked to the reduced levels of anti-flagellin antibodies in the TLR5(-/-) host. A variety of human TLR5 gene alleles exist that also associated with inflammatory conditions and may do so via effects on the gut microbiome and altered host-microbial crosstalk.

Keywords: Adaptive immunity; Allelic variation; Gut microbiome; Metagenomics; TLR5; Toll-like receptor 5.

Publication types

  • Review

MeSH terms

  • Adaptive Immunity
  • Animals
  • Antibody Formation / genetics
  • Flagellin / genetics
  • Flagellin / immunology
  • Flagellin / metabolism*
  • Gene Expression Regulation, Bacterial / genetics
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Humans
  • Immunity, Innate
  • Inflammation / genetics
  • Inflammation / immunology*
  • Inflammation / microbiology
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / microbiology
  • Mice
  • Mice, Knockout
  • Microbiota*
  • Toll-Like Receptor 5 / genetics
  • Toll-Like Receptor 5 / metabolism*

Substances

  • Toll-Like Receptor 5
  • Flagellin