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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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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. |
format | Online Article Text |
id | pubmed-3351431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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