Human colonic mucus is a reservoir for antimicrobial peptides

J Crohns Colitis. 2013 Dec;7(12):e652-64. doi: 10.1016/j.crohns.2013.05.006. Epub 2013 Jun 17.

Abstract

Background and aims: To prevent bacterial adherence and translocation, the colonic mucosa is covered by a protecting mucus layer and the epithelium synthesizes antimicrobial peptides. The present qualitative study investigated the contents and interaction of these peptides in and with rectal mucus.

Methods: Rectal mucus extracts were analyzed for antimicrobial activity and screened with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, Dot blot and immunohistochemistry for antimicrobial peptides. In addition, binding of AMPs to mucins was investigated by Western blot and enzyme-linked lectin assays.

Results: In functional tests the mucus layer exhibited a strong antimicrobial activity. We detected 11 antimicrobial peptides in mucus extracts from healthy persons including the defensins HBD-1 and -3, the cathelicidin LL-37, ubiquitin, lysozyme, histones, high mobility group nucleosome-binding domain-containing protein 2, ubiquicidin and other ribosomal proteins. AMPs were bound by mucins but this was demonstrated to be reversible and inhibition of antibacterial activity was limited.

Conclusion: These findings indicate that epithelial antimicrobial peptides are retained in the intestinal mucus layer without losing their efficacy. Thus, the mucus layer and its composition provide an attractive drug target to restore antimicrobial barrier function in intestinal diseases.

Keywords: AMP; Antimicrobial peptides;; ELLA; HMGN2; Inflammatory bowel disease;; Large intestine; MALDI-TOF-MS; Mucus;; RP-HPLC; antimicrobial peptide; enzyme-linked lectin assay; high mobility group nucleosome-binding domain-containing protein 2; matrix-assisted laser desorption/ionization time-of-flight mass spectrometry; reversed-phase high-performance liquid chromatography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Infective Agents / analysis*
  • Bacteroides fragilis / growth & development
  • Candida albicans / growth & development
  • Cathelicidins / analysis
  • Cathelicidins / metabolism
  • Defensins / analysis
  • Defensins / metabolism
  • Enterococcus faecalis / growth & development
  • Escherichia coli / growth & development
  • Flow Cytometry
  • HMGN2 Protein / analysis
  • HMGN2 Protein / metabolism
  • Histones / analysis
  • Histones / metabolism
  • Humans
  • Intestinal Mucosa / chemistry*
  • Microbial Sensitivity Tests
  • Mucins / metabolism
  • Mucus / chemistry*
  • Mucus / metabolism
  • Muramidase / analysis
  • Muramidase / metabolism
  • Peptides / analysis*
  • Peptides / metabolism*
  • Rectum / chemistry*
  • Ribosomal Proteins / analysis
  • Ribosomal Proteins / metabolism
  • Staphylococcus aureus / growth & development
  • Ubiquitin / analysis
  • Ubiquitin / metabolism

Substances

  • Anti-Infective Agents
  • Cathelicidins
  • Defensins
  • HMGN2 Protein
  • Histones
  • Mucins
  • Peptides
  • Ribosomal Proteins
  • Ubiquitin
  • ribosomal protein S30
  • Muramidase