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An expanded regulatory network temporally controls C andida albicans biofilm formation
C andida albicans biofilms are composed of highly adherent and densely arranged cells with properties distinct from those of free‐floating (planktonic) cells. These biofilms are a significant medical problem because they commonly form on implanted medical devices, are drug resistant and are difficul...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464956/ https://www.ncbi.nlm.nih.gov/pubmed/25784162 http://dx.doi.org/10.1111/mmi.13002 |
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author | Fox, Emily P. Bui, Catherine K. Nett, Jeniel E. Hartooni, Nairi Mui, Michael C. Andes, David R. Nobile, Clarissa J. Johnson, Alexander D. |
author_facet | Fox, Emily P. Bui, Catherine K. Nett, Jeniel E. Hartooni, Nairi Mui, Michael C. Andes, David R. Nobile, Clarissa J. Johnson, Alexander D. |
author_sort | Fox, Emily P. |
collection | PubMed |
description | C andida albicans biofilms are composed of highly adherent and densely arranged cells with properties distinct from those of free‐floating (planktonic) cells. These biofilms are a significant medical problem because they commonly form on implanted medical devices, are drug resistant and are difficult to remove. C . albicans biofilms are not static structures; rather they are dynamic and develop over time. Here we characterize gene expression in biofilms during their development, and by comparing them to multiple planktonic reference states, we identify patterns of gene expression relevant to biofilm formation. In particular, we document time‐dependent changes in genes involved in adhesion and metabolism, both of which are at the core of biofilm development. Additionally, we identify three new regulators of biofilm formation, Flo8, Gal4, and Rfx2, which play distinct roles during biofilm development over time. Flo8 is required for biofilm formation at all time points, and Gal4 and Rfx2 are needed for proper biofilm formation at intermediate time points. |
format | Online Article Text |
id | pubmed-4464956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44649562015-06-13 An expanded regulatory network temporally controls C andida albicans biofilm formation Fox, Emily P. Bui, Catherine K. Nett, Jeniel E. Hartooni, Nairi Mui, Michael C. Andes, David R. Nobile, Clarissa J. Johnson, Alexander D. Mol Microbiol Research Articles C andida albicans biofilms are composed of highly adherent and densely arranged cells with properties distinct from those of free‐floating (planktonic) cells. These biofilms are a significant medical problem because they commonly form on implanted medical devices, are drug resistant and are difficult to remove. C . albicans biofilms are not static structures; rather they are dynamic and develop over time. Here we characterize gene expression in biofilms during their development, and by comparing them to multiple planktonic reference states, we identify patterns of gene expression relevant to biofilm formation. In particular, we document time‐dependent changes in genes involved in adhesion and metabolism, both of which are at the core of biofilm development. Additionally, we identify three new regulators of biofilm formation, Flo8, Gal4, and Rfx2, which play distinct roles during biofilm development over time. Flo8 is required for biofilm formation at all time points, and Gal4 and Rfx2 are needed for proper biofilm formation at intermediate time points. John Wiley and Sons Inc. 2015-06 2015-04-23 /pmc/articles/PMC4464956/ /pubmed/25784162 http://dx.doi.org/10.1111/mmi.13002 Text en © 2015 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Fox, Emily P. Bui, Catherine K. Nett, Jeniel E. Hartooni, Nairi Mui, Michael C. Andes, David R. Nobile, Clarissa J. Johnson, Alexander D. An expanded regulatory network temporally controls C andida albicans biofilm formation |
title | An expanded regulatory network temporally controls C
andida albicans biofilm formation |
title_full | An expanded regulatory network temporally controls C
andida albicans biofilm formation |
title_fullStr | An expanded regulatory network temporally controls C
andida albicans biofilm formation |
title_full_unstemmed | An expanded regulatory network temporally controls C
andida albicans biofilm formation |
title_short | An expanded regulatory network temporally controls C
andida albicans biofilm formation |
title_sort | expanded regulatory network temporally controls c
andida albicans biofilm formation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464956/ https://www.ncbi.nlm.nih.gov/pubmed/25784162 http://dx.doi.org/10.1111/mmi.13002 |
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