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The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro
To better understand the molecular events underlying vulvovaginal candidiasis, we established an in vitro system. Immortalized vaginal epithelial cells were infected with live, yeast form C. albicans and C. albicans cultured in the same medium without vaginal epithelial cells were used as control. I...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558442/ https://www.ncbi.nlm.nih.gov/pubmed/26366412 http://dx.doi.org/10.1155/2015/398045 |
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author | Manczinger, Máté Bocsik, Alexandra Kocsis, Gabriella F. Vörös, Andrea Hegedűs, Zoltán Ördögh, Lilla Kondorosi, Éva Marton, Annamária Vízler, Csaba Tubak, Vilmos Deli, Mária Kemény, Lajos Nagy, István Lakatos, Lóránt |
author_facet | Manczinger, Máté Bocsik, Alexandra Kocsis, Gabriella F. Vörös, Andrea Hegedűs, Zoltán Ördögh, Lilla Kondorosi, Éva Marton, Annamária Vízler, Csaba Tubak, Vilmos Deli, Mária Kemény, Lajos Nagy, István Lakatos, Lóránt |
author_sort | Manczinger, Máté |
collection | PubMed |
description | To better understand the molecular events underlying vulvovaginal candidiasis, we established an in vitro system. Immortalized vaginal epithelial cells were infected with live, yeast form C. albicans and C. albicans cultured in the same medium without vaginal epithelial cells were used as control. In both cases a yeast to hyphae transition was robustly induced. Whole transcriptome sequencing was used to identify specific gene expression changes in C. albicans. Numerous genes leading to a yeast to hyphae transition and hyphae specific genes were upregulated in the control hyphae and the hyphae in response to vaginal epithelial cells. Strikingly, the GlcNAc pathway was exclusively triggered by vaginal epithelial cells. Functional analysis in our in vitro system revealed that the GlcNAc biosynthesis is involved in the adherence to, and the ability to kill, vaginal epithelial cells in vitro, thus indicating the key role for this pathway in the virulence of C. albicans upon vulvovaginal candidiasis. |
format | Online Article Text |
id | pubmed-4558442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-45584422015-09-13 The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro Manczinger, Máté Bocsik, Alexandra Kocsis, Gabriella F. Vörös, Andrea Hegedűs, Zoltán Ördögh, Lilla Kondorosi, Éva Marton, Annamária Vízler, Csaba Tubak, Vilmos Deli, Mária Kemény, Lajos Nagy, István Lakatos, Lóránt Biomed Res Int Research Article To better understand the molecular events underlying vulvovaginal candidiasis, we established an in vitro system. Immortalized vaginal epithelial cells were infected with live, yeast form C. albicans and C. albicans cultured in the same medium without vaginal epithelial cells were used as control. In both cases a yeast to hyphae transition was robustly induced. Whole transcriptome sequencing was used to identify specific gene expression changes in C. albicans. Numerous genes leading to a yeast to hyphae transition and hyphae specific genes were upregulated in the control hyphae and the hyphae in response to vaginal epithelial cells. Strikingly, the GlcNAc pathway was exclusively triggered by vaginal epithelial cells. Functional analysis in our in vitro system revealed that the GlcNAc biosynthesis is involved in the adherence to, and the ability to kill, vaginal epithelial cells in vitro, thus indicating the key role for this pathway in the virulence of C. albicans upon vulvovaginal candidiasis. Hindawi Publishing Corporation 2015 2015-08-20 /pmc/articles/PMC4558442/ /pubmed/26366412 http://dx.doi.org/10.1155/2015/398045 Text en Copyright © 2015 Máté Manczinger et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Manczinger, Máté Bocsik, Alexandra Kocsis, Gabriella F. Vörös, Andrea Hegedűs, Zoltán Ördögh, Lilla Kondorosi, Éva Marton, Annamária Vízler, Csaba Tubak, Vilmos Deli, Mária Kemény, Lajos Nagy, István Lakatos, Lóránt The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro |
title | The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro
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title_full | The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro
|
title_fullStr | The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro
|
title_full_unstemmed | The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro
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title_short | The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro
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title_sort | absence of n-acetyl-d-glucosamine causes attenuation of virulence of candida albicans upon interaction with vaginal epithelial cells in vitro |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558442/ https://www.ncbi.nlm.nih.gov/pubmed/26366412 http://dx.doi.org/10.1155/2015/398045 |
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