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Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic

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...

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Autores principales: Božić, Aleksandar, Anderson, Robin C., Crippen, Tawni L., Swaggerty, Christina L., Hume, Michael E., Beier, Ross C., He, Haiqi, Genovese, Kenneth J., Poole, Toni L., Harvey, Roger B., Nisbet, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409177/
https://www.ncbi.nlm.nih.gov/pubmed/32679904
http://dx.doi.org/10.3390/microorganisms8071051
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author Božić, Aleksandar
Anderson, Robin C.
Crippen, Tawni L.
Swaggerty, Christina L.
Hume, Michael E.
Beier, Ross C.
He, Haiqi
Genovese, Kenneth J.
Poole, Toni L.
Harvey, Roger B.
Nisbet, David J.
author_facet Božić, Aleksandar
Anderson, Robin C.
Crippen, Tawni L.
Swaggerty, Christina L.
Hume, Michael E.
Beier, Ross C.
He, Haiqi
Genovese, Kenneth J.
Poole, Toni L.
Harvey, Roger B.
Nisbet, David J.
author_sort Božić, Aleksandar
collection PubMed
description 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 log(10) 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.
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spelling pubmed-74091772020-08-26 Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic Božić, Aleksandar Anderson, Robin C. Crippen, Tawni L. Swaggerty, Christina L. Hume, Michael E. Beier, Ross C. He, Haiqi Genovese, Kenneth J. Poole, Toni L. Harvey, Roger B. Nisbet, David J. Microorganisms Article 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 log(10) 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. MDPI 2020-07-15 /pmc/articles/PMC7409177/ /pubmed/32679904 http://dx.doi.org/10.3390/microorganisms8071051 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Božić, Aleksandar
Anderson, Robin C.
Crippen, Tawni L.
Swaggerty, Christina L.
Hume, Michael E.
Beier, Ross C.
He, Haiqi
Genovese, Kenneth J.
Poole, Toni L.
Harvey, Roger B.
Nisbet, David J.
Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic
title Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic
title_full Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic
title_fullStr Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic
title_full_unstemmed Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic
title_short Inhibition of Salmonella Binding to Porcine Intestinal Cells by a Wood-Derived Prebiotic
title_sort inhibition of salmonella binding to porcine intestinal cells by a wood-derived prebiotic
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409177/
https://www.ncbi.nlm.nih.gov/pubmed/32679904
http://dx.doi.org/10.3390/microorganisms8071051
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