E. coli O124 K72 alters the intestinal barrier and the tight junctions proteins of guinea pig intestine

Biomed Pharmacother. 2017 Oct:94:468-473. doi: 10.1016/j.biopha.2017.07.123. Epub 2017 Aug 2.

Abstract

Our research group previously isolated and identified a strain of pathogenic Escherichia coli from clinical samples called E. coli O124 K72. The present study was aimed at determining the potential effects of E. coli O124 K72 on intestinal barrier functions and structural proteins integrity in guinea pig. Guinea pigs were grouped into three groups; control (CG); E. coli O124 K72 (E. coli); and probiotics Lactobacillus rhamnosus (LGG). Initially, we create intestinal dysbiosis by giving all animals Levofloxacin for 10days, but the control group (CG) received the same volume of saline. Then, the animals received either E. coli O124 K72 (E. coli) or Lactobacillus rhamnosus (LGG) according to their assigned group. E. coli O124 K72 treatment significantly affected colon morphology and distorted intestinal barrier function by up-regulating Claudin2 and down-regulating Occludin. In addition, E. coli upregulated the mRNA expression of MUC1, MUC2, MUC13 and MUC15. Furthermore, suspected tumor was found in the E. coli treated animals. Our results suggested that E. coli O124 K72 strain has adverse effects on intestinal barrier functions and is capable of altering integrity of structural proteins in guinea pig model while at same time it may have a role in colon carcinogenesis.

Keywords: Antibiotic; E. coli O124 K72; Intestinal barrier; Mucin.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Claudin-2 / metabolism
  • Denaturing Gradient Gel Electrophoresis
  • Disease Models, Animal
  • Dysbiosis / drug therapy
  • Dysbiosis / metabolism
  • Dysbiosis / microbiology
  • Dysbiosis / pathology
  • Escherichia coli / physiology*
  • Gastrointestinal Microbiome
  • Guinea Pigs
  • Intestines / drug effects
  • Intestines / microbiology*
  • Intestines / pathology*
  • Mucin-2 / metabolism
  • Occludin / metabolism
  • Tight Junction Proteins / metabolism*

Substances

  • Anti-Bacterial Agents
  • Claudin-2
  • Mucin-2
  • Occludin
  • Tight Junction Proteins