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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
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.
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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
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
title_short The Absence of N-Acetyl-D-glucosamine Causes Attenuation of Virulence of Candida albicans upon Interaction with Vaginal Epithelial Cells In Vitro
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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