Mucin dynamics in intestinal bacterial infection

PLoS One. 2008;3(12):e3952. doi: 10.1371/journal.pone.0003952. Epub 2008 Dec 17.


Background: Bacterial gastroenteritis causes morbidity and mortality in humans worldwide. Murine Citrobacter rodentium infection is a model for gastroenteritis caused by the human pathogens enteropathogenic Escherichia coli and enterohaemorrhagic E. coli. Mucin glycoproteins are the main component of the first barrier that bacteria encounter in the intestinal tract.

Methodology/principal findings: Using Immunohistochemistry, we investigated intestinal expression of mucins (Alcian blue/PAS, Muc1, Muc2, Muc4, Muc5AC, Muc13 and Muc3/17) in healthy and C. rodentium infected mice. The majority of the C. rodentium infected mice developed systemic infection and colitis in the mid and distal colon by day 12. C. rodentium bound to the major secreted mucin, Muc2, in vitro, and high numbers of bacteria were found in secreted MUC2 in infected animals in vivo, indicating that mucins may limit bacterial access to the epithelial surface. In the small intestine, caecum and proximal colon, the mucin expression was similar in infected and non-infected animals. In the distal colonic epithelium, all secreted and cell surface mucins decreased with the exception of the Muc1 cell surface mucin which increased after infection (p<0.05). Similarly, during human infection Salmonella St Paul, Campylobacter jejuni and Clostridium difficile induced MUC1 in the colon.

Conclusion: Major changes in both the cell-surface and secreted mucins occur in response to intestinal infection.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Cecum / microbiology
  • Cecum / pathology
  • Citrobacter rodentium / isolation & purification
  • Citrobacter rodentium / physiology
  • Enterobacteriaceae Infections / complications
  • Enterobacteriaceae Infections / metabolism*
  • Enterobacteriaceae Infections / pathology
  • Female
  • Humans
  • Intestinal Diseases / etiology
  • Intestinal Diseases / metabolism*
  • Intestinal Diseases / pathology
  • Intestine, Large / microbiology
  • Intestine, Large / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Mucins / metabolism*
  • Tissue Distribution
  • Young Adult


  • Mucins