Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic.
Aleksandar BožićRobin C AndersonTawni L CrippenChristina L SwaggertyMichael E HumeRoss C BeierHaiqi HeKenneth J GenoveseToni L PooleRoger B HarveyDavid J NisbetPublished in: Microorganisms (2020)
Numerous Salmonella enterica serovars can cause disease and contamination of animal-produced foods. Oligosaccharide-rich products capable of blocking pathogen adherence to intestinal mucosa are attractive alternatives to antibiotics as these have potential to prevent enteric infections. Presently, a wood-derived prebiotic composed mainly of glucose-galactose-mannose-xylose oligomers was found to inhibit mannose-sensitive binding of select Salmonella Typhimurium and Escherichia coli strains when reacted with Saccharomyces boulardii. Tests for the ability of the prebiotic to prevent binding of a green fluorescent protein (GFP)-labeled S. Typhimurium to intestinal porcine epithelial cells (IPEC-J2) cultured in vitro revealed that prebiotic-exposed GFP-labeled S. Typhimurium bound > 30% fewer individual IPEC-J2 cells than did GFP-labeled S. Typhimurium having no prebiotic exposure. Quantitatively, 90% fewer prebiotic-exposed GFP-labeled S. Typhimurium cells were bound per individual IPEC-J2 cell compared to non-prebiotic exposed GFP-labeled S. Typhimurium. Comparison of invasiveness of S. Typhimurium DT104 against IPEC-J2 cells revealed greater than a 90% decrease in intracellular recovery of prebiotic-exposed S. Typhimurium DT104 compared to non-exposed controls (averaging 4.4 ± 0.2 log10 CFU/well). These results suggest compounds within the wood-derived prebiotic bound to E. coli and S. Typhimurium-produced adhesions and in the case of S. Typhimurium, this adhesion-binding activity inhibited the binding and invasion of IPEC-J2 cells.
Keyphrases
- listeria monocytogenes
- escherichia coli
- induced apoptosis
- cell cycle arrest
- stem cells
- risk assessment
- single cell
- oxidative stress
- type diabetes
- endothelial cells
- computed tomography
- blood pressure
- metabolic syndrome
- binding protein
- klebsiella pneumoniae
- pseudomonas aeruginosa
- bone marrow
- drinking water
- quantum dots
- blood glucose
- positron emission tomography
- health risk
- single molecule
- living cells
- clinical evaluation