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Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process

Candida albicans frequently causes superficial infections by invading and damaging epithelial cells, but may also cause systemic infections by penetrating through epithelial barriers. C. albicans is a remarkable pathogen because it can invade epithelial cells via two distinct mechanisms: induced end...

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Autores principales: Wächtler, Betty, Citiulo, Francesco, Jablonowski, Nadja, Förster, Stephanie, Dalle, Frederic, Schaller, Martin, Wilson, Duncan, Hube, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351431/
https://www.ncbi.nlm.nih.gov/pubmed/22606314
http://dx.doi.org/10.1371/journal.pone.0036952
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author Wächtler, Betty
Citiulo, Francesco
Jablonowski, Nadja
Förster, Stephanie
Dalle, Frederic
Schaller, Martin
Wilson, Duncan
Hube, Bernhard
author_facet Wächtler, Betty
Citiulo, Francesco
Jablonowski, Nadja
Förster, Stephanie
Dalle, Frederic
Schaller, Martin
Wilson, Duncan
Hube, Bernhard
author_sort Wächtler, Betty
collection PubMed
description Candida albicans frequently causes superficial infections by invading and damaging epithelial cells, but may also cause systemic infections by penetrating through epithelial barriers. C. albicans is a remarkable pathogen because it can invade epithelial cells via two distinct mechanisms: induced endocytosis, analogous to facultative intracellular enteropathogenic bacteria, and active penetration, similar to plant pathogenic fungi. Here we investigated the contributions of the two invasion routes of C. albicans to epithelial invasion. Using selective cellular inhibition approaches and differential fluorescence microscopy, we demonstrate that induced endocytosis contributes considerably to the early time points of invasion, while active penetration represents the dominant epithelial invasion route. Although induced endocytosis depends mainly on Als3-E–cadherin interactions, we observed E–cadherin independent induced endocytosis. Finally, we provide evidence of a protective role for serum factors in oral infection: human serum strongly inhibited C. albicans adhesion to, invasion and damage of oral epithelial cells.
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spelling pubmed-33514312012-05-17 Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process Wächtler, Betty Citiulo, Francesco Jablonowski, Nadja Förster, Stephanie Dalle, Frederic Schaller, Martin Wilson, Duncan Hube, Bernhard PLoS One Research Article Candida albicans frequently causes superficial infections by invading and damaging epithelial cells, but may also cause systemic infections by penetrating through epithelial barriers. C. albicans is a remarkable pathogen because it can invade epithelial cells via two distinct mechanisms: induced endocytosis, analogous to facultative intracellular enteropathogenic bacteria, and active penetration, similar to plant pathogenic fungi. Here we investigated the contributions of the two invasion routes of C. albicans to epithelial invasion. Using selective cellular inhibition approaches and differential fluorescence microscopy, we demonstrate that induced endocytosis contributes considerably to the early time points of invasion, while active penetration represents the dominant epithelial invasion route. Although induced endocytosis depends mainly on Als3-E–cadherin interactions, we observed E–cadherin independent induced endocytosis. Finally, we provide evidence of a protective role for serum factors in oral infection: human serum strongly inhibited C. albicans adhesion to, invasion and damage of oral epithelial cells. Public Library of Science 2012-05-14 /pmc/articles/PMC3351431/ /pubmed/22606314 http://dx.doi.org/10.1371/journal.pone.0036952 Text en Wächtler 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
Wächtler, Betty
Citiulo, Francesco
Jablonowski, Nadja
Förster, Stephanie
Dalle, Frederic
Schaller, Martin
Wilson, Duncan
Hube, Bernhard
Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process
title Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process
title_full Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process
title_fullStr Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process
title_full_unstemmed Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process
title_short Candida albicans-Epithelial Interactions: Dissecting the Roles of Active Penetration, Induced Endocytosis and Host Factors on the Infection Process
title_sort candida albicans-epithelial interactions: dissecting the roles of active penetration, induced endocytosis and host factors on the infection process
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351431/
https://www.ncbi.nlm.nih.gov/pubmed/22606314
http://dx.doi.org/10.1371/journal.pone.0036952
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