Bacillus cereus NVH 0500/00 Can Adhere to Mucin but Cannot Produce Enterotoxins during Gastrointestinal Simulation

Varvara Tsilia1, Frederiek-Maarten Kerckhof2, Andreja Rajkovic3

  • 1Laboratory of Microbial Ecology and Technology (LabMET), Department of Biochemical and Microbial Technology, Ghent University, Ghent, Belgium Laboratory of Food Microbiology and Food Preservation (LFMFP), Department of Food Safety and Food Quality, Ghent University, Ghent, Belgium.

Insights

Bacillus cereus adheres to intestinal mucin, potentially aiding its survival and transport through the gut. Mucin may also protect bacterial toxins from degradation in the intestines.

Area of Science:

  • Microbiology
  • Gastroenterology
  • Food Science

Background:

  • Intestinal adhesion is a key factor in Bacillus cereus pathogenesis.
  • Mucin glycoproteins in the gut lining protect enterocytes and can serve as bacterial nutrient and attachment sites.

Purpose of the Study:

  • To investigate the in vitro adhesion of Bacillus cereus to mucin under simulated gastrointestinal conditions.
  • To evaluate the stability of nonhemolytic enterotoxin (Nhe) when exposed to intestinal components in the presence of mucin.

Main Methods:

  • In vitro exposure of Bacillus cereus to low pH and intestinal components (bile, pancreatin).
  • Mucin adhesion assay to determine bacterial attachment and persistence after simulated gut emptying.
  • Investigation of Nhe stability on mucin agar.

Main Results:

  • Bacillus cereus grew and adhered to mucin during in vitro ileal incubation, showing resilience to prior pH and intestinal component exposure.
  • Final bacterial concentration reached 6.62 ± 0.87 log CFU ml(-1) with approximately 6% adhesion.
  • No enterotoxin was detected in the ileum, likely due to low bacterial load or Nhe degradation.

Conclusions:

  • Mucin retains Bacillus cereus and facilitates its passage into the small intestine.
  • Mucin may protect bacterial enterotoxins from degradation by intestinal factors, potentially influencing pathogenesis.