New in vitro colonic fermentation model for Salmonella infection in the child gut

Gwenaëlle Le Blay1, Julia Rytka, Annina Zihler

  • 1Laboratory of Food Biotechnology, Institute of Food Science and Nutrition, Zurich, Switzerland.

FEMS Microbiology Ecology
|December 18, 2008
PubMed

Insights

A new in vitro model simulates Salmonella infection in the child gut. Amoxicillin reduced Salmonella, but the pathogen returned after treatment, mimicking in vivo results and aiding antimicrobial development.

Area of Science:

  • Microbiology
  • Gastroenterology
  • Pharmacology

Background:

  • Salmonella infections are a significant public health concern, particularly in children.
  • Understanding gut microbiota dynamics during infection and antibiotic treatment is crucial for developing effective therapies.

Purpose of the Study:

  • To develop and validate an in vitro continuous colonic fermentation model simulating Salmonella infection.
  • To assess the impact of amoxicillin on gut microbiota composition, metabolism, and Salmonella Typhimurium levels.

Main Methods:

  • Development of a proximal colon fermentation model using immobilized child fecal microbiota and Salmonella Typhimurium.
  • Application of two amoxicillin concentrations (90 and 180 mg/day) over a 43-day fermentation period.
  • Monitoring of Salmonella concentrations, microbial populations (Enterobacteriaceae, Clostridium coccoides-Eubacterium rectale, Atopobium, Bifidobacteria), and metabolic activity.

Main Results:

  • The model established a stable Salmonella Typhimurium concentration (log 7.5 cells/mL) and altered microbial populations.
  • Amoxicillin treatment decreased Salmonella levels and shifted microbial balance, reducing C. coccoides-E. rectale and increasing Enterobacteriaceae.
  • Salmonella levels rebounded upon cessation of amoxicillin, mirroring in vivo observations of Salmonella shedding.

Conclusions:

  • The developed in vitro model accurately simulates Salmonella infection and amoxicillin effects in the pediatric gut.
  • This model serves as a valuable tool for evaluating antimicrobials against enteropathogens.
  • Findings highlight the dynamic interplay between microbiota, pathogen, and antibiotics in the colonic environment.

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