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The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage

BACKGROUND: Mixed intestinal infections with Entamoeba histolytica, Entamoeba dispar and bacteria with exacerbated manifestations of disease are common in regions where amoebiasis is endemic. However, amoeba–bacteria interactions remain largely unexamined. METHODOLOGY: Trophozoites of E. histolytica...

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Autores principales: Galván-Moroyoqui, José Manuel, Domínguez-Robles, M. del Carmen, Franco, Elizabeth, Meza, Isaura
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447883/
https://www.ncbi.nlm.nih.gov/pubmed/18648517
http://dx.doi.org/10.1371/journal.pntd.0000266
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author Galván-Moroyoqui, José Manuel
Domínguez-Robles, M. del Carmen
Franco, Elizabeth
Meza, Isaura
author_facet Galván-Moroyoqui, José Manuel
Domínguez-Robles, M. del Carmen
Franco, Elizabeth
Meza, Isaura
author_sort Galván-Moroyoqui, José Manuel
collection PubMed
description BACKGROUND: Mixed intestinal infections with Entamoeba histolytica, Entamoeba dispar and bacteria with exacerbated manifestations of disease are common in regions where amoebiasis is endemic. However, amoeba–bacteria interactions remain largely unexamined. METHODOLOGY: Trophozoites of E. histolytica and E. dispar were co-cultured with enteropathogenic bacteria strains Escherichia coli (EPEC), Shigella dysenteriae and a commensal Escherichia coli. Amoebae that phagocytosed bacteria were tested for a cytopathic effect on epithelial cell monolayers. Cysteine proteinase activity, adhesion and cell surface concentration of Gal/GalNAc lectin were analyzed in amoebae showing increased virulence. Structural and functional changes and induction of IL-8 expression were determined in epithelial cells before and after exposure to bacteria. Chemotaxis of amoebae and neutrophils to human IL-8 and conditioned culture media from epithelial cells exposed to bacteria was quantified. PRINCIPAL FINDINGS: E. histolytica digested phagocytosed bacteria, although S. dysenteriae retained 70% viability after ingestion. Phagocytosis of pathogenic bacteria augmented the cytopathic effect of E. histolytica and increased expression of Gal/GalNAc lectin on the amoebic surface and increased cysteine proteinase activity. E. dispar remained avirulent. Adhesion of amoebae and damage to cells exposed to bacteria were increased. Additional increases were observed if amoebae had phagocytosed bacteria. Co-culture of epithelial cells with enteropathogenic bacteria disrupted monolayer permeability and induced expression of IL-8. Media from these co-cultures and human recombinant IL-8 were similarly chemotactic for neutrophils and E. histolytica. CONCLUSIONS: Epithelial monolayers exposed to enteropathogenic bacteria become more susceptible to E. histolytica damage. At the same time, phagocytosis of pathogenic bacteria by amoebae further increased epithelial cell damage. SIGNIFICANCE: The in vitro system presented here provides evidence that the Entamoeba/enteropathogenic bacteria interplay modulates epithelial cell responses to the pathogens. In mixed intestinal infections, where such interactions are possible, they could influence the outcome of disease. The results offer insights to continue research on this phenomenon.
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spelling pubmed-24478832008-07-23 The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage Galván-Moroyoqui, José Manuel Domínguez-Robles, M. del Carmen Franco, Elizabeth Meza, Isaura PLoS Negl Trop Dis Research Article BACKGROUND: Mixed intestinal infections with Entamoeba histolytica, Entamoeba dispar and bacteria with exacerbated manifestations of disease are common in regions where amoebiasis is endemic. However, amoeba–bacteria interactions remain largely unexamined. METHODOLOGY: Trophozoites of E. histolytica and E. dispar were co-cultured with enteropathogenic bacteria strains Escherichia coli (EPEC), Shigella dysenteriae and a commensal Escherichia coli. Amoebae that phagocytosed bacteria were tested for a cytopathic effect on epithelial cell monolayers. Cysteine proteinase activity, adhesion and cell surface concentration of Gal/GalNAc lectin were analyzed in amoebae showing increased virulence. Structural and functional changes and induction of IL-8 expression were determined in epithelial cells before and after exposure to bacteria. Chemotaxis of amoebae and neutrophils to human IL-8 and conditioned culture media from epithelial cells exposed to bacteria was quantified. PRINCIPAL FINDINGS: E. histolytica digested phagocytosed bacteria, although S. dysenteriae retained 70% viability after ingestion. Phagocytosis of pathogenic bacteria augmented the cytopathic effect of E. histolytica and increased expression of Gal/GalNAc lectin on the amoebic surface and increased cysteine proteinase activity. E. dispar remained avirulent. Adhesion of amoebae and damage to cells exposed to bacteria were increased. Additional increases were observed if amoebae had phagocytosed bacteria. Co-culture of epithelial cells with enteropathogenic bacteria disrupted monolayer permeability and induced expression of IL-8. Media from these co-cultures and human recombinant IL-8 were similarly chemotactic for neutrophils and E. histolytica. CONCLUSIONS: Epithelial monolayers exposed to enteropathogenic bacteria become more susceptible to E. histolytica damage. At the same time, phagocytosis of pathogenic bacteria by amoebae further increased epithelial cell damage. SIGNIFICANCE: The in vitro system presented here provides evidence that the Entamoeba/enteropathogenic bacteria interplay modulates epithelial cell responses to the pathogens. In mixed intestinal infections, where such interactions are possible, they could influence the outcome of disease. The results offer insights to continue research on this phenomenon. Public Library of Science 2008-07-23 /pmc/articles/PMC2447883/ /pubmed/18648517 http://dx.doi.org/10.1371/journal.pntd.0000266 Text en Galván-Moroyoqui et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Galván-Moroyoqui, José Manuel
Domínguez-Robles, M. del Carmen
Franco, Elizabeth
Meza, Isaura
The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage
title The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage
title_full The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage
title_fullStr The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage
title_full_unstemmed The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage
title_short The Interplay between Entamoeba and Enteropathogenic Bacteria Modulates Epithelial Cell Damage
title_sort interplay between entamoeba and enteropathogenic bacteria modulates epithelial cell damage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447883/
https://www.ncbi.nlm.nih.gov/pubmed/18648517
http://dx.doi.org/10.1371/journal.pntd.0000266
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