Pectins that Structurally Differ in the Distribution of Methyl-Esters Attenuate Citrobacter rodentium-Induced Colitis

Mol Nutr Food Res. 2021 Oct;65(19):e2100346. doi: 10.1002/mnfr.202100346. Epub 2021 Aug 16.

Abstract

Introduction: Pectins have anti-inflammatory properties on intestinal immunity through direct interactions on Toll-like receptors (TLRs) in the small intestine or via stimulating microbiota-dependent effects in the large intestine. Both the degree of methyl-esterification (DM) and the distribution of methyl-esters (degree of blockiness; DB) of pectins contribute to this influence on immunity, but whether and how the DB impacts immunity through microbiota-dependent effects in the large intestine is unknown. Therefore, this study tests pectins that structurally differ in DB in a mouse model with Citrobacter rodentium induced colitis and studies the impact on the intestinal microbiota composition and associated attenuation of inflammation.

Methods and results: Both low and high DB pectins induce a more rich and diverse microbiota composition. These pectins also lower the bacterial load of C. rodentium in cecal digesta. Through these effects, both low and high DB pectins attenuate C. rodentium induced colitis resulting in reduced intestinal damage, reduced numbers of Th1-cells, which are increased in case of C. rodentium induced colitis, and reduced levels of GATA3+ Tregs, which are related to tissue inflammation.

Conclusion: Pectins prevent C. rodentium induced colonic inflammation by lowering the C. rodentium load in the caecum independently of the DB.

Keywords: Citrobacter rodentium; colitis; degree of blockiness; degree of methyl-esterification; microbiota; pectin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Cecum / drug effects
  • Cecum / metabolism
  • Citrobacter rodentium / pathogenicity
  • Citrus sinensis / chemistry
  • Colitis / drug therapy*
  • Colitis / microbiology
  • Colitis / pathology
  • Cytokines / metabolism
  • Enterobacteriaceae Infections / drug therapy*
  • Enterobacteriaceae Infections / pathology
  • Esters / chemistry
  • Female
  • Gastrointestinal Microbiome / drug effects
  • Gastrointestinal Microbiome / genetics
  • Mice
  • Mice, Inbred C57BL
  • Pectins / chemistry*
  • Pectins / pharmacology*
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / pathology

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • Esters
  • Pectins