Streptococcus thermophilus NCIMB 41856 ameliorates signs of colitis in an animal model of inflammatory bowel disease

Benef Microbes. 2017 Aug 24;8(4):605-614. doi: 10.3920/BM2016.0110. Epub 2017 Jun 16.

Abstract

Treatment of inflammatory bowel disease (IBD) is mainly based on suppression of symptoms, often with numerous side effects. Trials of probiotics in IBD have frequently produced disappointing results. The majority of probiotics are unusual, since they do not require iron for growth, unlike many bacteria resident in the intestine. The IBD intestine is iron-rich due to bleeding and use of oral iron supplements; conventional probiotics would be rapidly outcompeted. We have evaluated an iron-responsive Streptococcus thermophilus strain for its potential to reduce signs of colitis. Efficacy of S. thermophilus was evaluated in the dextran sodium sulphate mouse model of colitis. Treated animals were given 1×108 cfu S. thermophilus per day and clinical observations were taken daily. At termination, gross and histopathological signs of disease, cellular infiltration, location of bacteria, and cytokine expression in the intestine were determined. S. thermophilus delayed onset of colitis and reduced clinical signs of disease, including bodyweight loss and gastrointestinal bleeding. It reduced bacterial translocation into the colonic tissue. Increased numbers of CD8+ intraepithelial lymphocytes were seen in control animals treated with S. thermophilus. S. thermophilus had no effect on gross pathology, histopathology or cytokine production in either colitic or control animals. We propose that S. thermophilus promotes maintenance of mucosal barrier function which reduces bacterial translocation, thereby reducing immune stimulation and associated inflammation. This allows mucosal healing, reducing gastrointestinal bleeding and weight loss. This could be studied as a locally-acting adjunct or alternative to current IBD treatments.

Keywords: epithelial barrier function; gastrointestinal bleeding; probiotic.

MeSH terms

  • Animals
  • Colitis, Ulcerative / drug therapy*
  • Colitis, Ulcerative / genetics
  • Colitis, Ulcerative / immunology
  • Cytokines / genetics
  • Cytokines / immunology
  • Disease Models, Animal
  • Humans
  • Intestines / drug effects
  • Intestines / immunology
  • Intestines / microbiology
  • Mice
  • Mice, Inbred BALB C
  • Probiotics / administration & dosage*
  • Streptococcus thermophilus / physiology*

Substances

  • Cytokines