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The Transcriptional Stress Response of Candida albicans to Weak Organic Acids

Candida albicans is the most important fungal pathogen of humans, causing severe infections, especially in nosocomial and immunocompromised settings. However, it is also the most prevalent fungus of the normal human microbiome, where it shares its habitat with hundreds of trillions of other microbia...

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Autores principales: Cottier, Fabien, Tan, Alrina Shin Min, Chen, Jinmiao, Lum, Josephine, Zolezzi, Francesca, Poidinger, Michael, Pavelka, Norman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390566/
https://www.ncbi.nlm.nih.gov/pubmed/25636313
http://dx.doi.org/10.1534/g3.114.015941
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author Cottier, Fabien
Tan, Alrina Shin Min
Chen, Jinmiao
Lum, Josephine
Zolezzi, Francesca
Poidinger, Michael
Pavelka, Norman
author_facet Cottier, Fabien
Tan, Alrina Shin Min
Chen, Jinmiao
Lum, Josephine
Zolezzi, Francesca
Poidinger, Michael
Pavelka, Norman
author_sort Cottier, Fabien
collection PubMed
description Candida albicans is the most important fungal pathogen of humans, causing severe infections, especially in nosocomial and immunocompromised settings. However, it is also the most prevalent fungus of the normal human microbiome, where it shares its habitat with hundreds of trillions of other microbial cells. Despite weak organic acids (WOAs) being among the most abundant metabolites produced by bacterial microbiota, little is known about their effect on C. albicans. Here we used a sequencing-based profiling strategy to systematically investigate the transcriptional stress response of C. albicans to lactic, acetic, propionic, and butyric acid at several time points after treatment. Our data reveal a complex transcriptional response, with individual WOAs triggering unique gene expression profiles and with important differences between acute and chronic exposure. Despite these dissimilarities, we found significant overlaps between the gene expression changes induced by each WOA, which led us to uncover a core transcriptional response that was largely unrelated to other previously published C. albicans transcriptional stress responses. Genes commonly up-regulated by WOAs were enriched in several iron transporters, which was associated with an overall decrease in intracellular iron concentrations. Moreover, chronic exposure to any WOA lead to down-regulation of RNA synthesis and ribosome biogenesis genes, which resulted in significant reduction of total RNA levels and of ribosomal RNA in particular. In conclusion, this study suggests that gastrointestinal microbiota might directly influence C. albicans physiology via production of WOAs, with possible implications of how this fungus interacts with its host in both health and disease.
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spelling pubmed-43905662015-04-10 The Transcriptional Stress Response of Candida albicans to Weak Organic Acids Cottier, Fabien Tan, Alrina Shin Min Chen, Jinmiao Lum, Josephine Zolezzi, Francesca Poidinger, Michael Pavelka, Norman G3 (Bethesda) Investigations Candida albicans is the most important fungal pathogen of humans, causing severe infections, especially in nosocomial and immunocompromised settings. However, it is also the most prevalent fungus of the normal human microbiome, where it shares its habitat with hundreds of trillions of other microbial cells. Despite weak organic acids (WOAs) being among the most abundant metabolites produced by bacterial microbiota, little is known about their effect on C. albicans. Here we used a sequencing-based profiling strategy to systematically investigate the transcriptional stress response of C. albicans to lactic, acetic, propionic, and butyric acid at several time points after treatment. Our data reveal a complex transcriptional response, with individual WOAs triggering unique gene expression profiles and with important differences between acute and chronic exposure. Despite these dissimilarities, we found significant overlaps between the gene expression changes induced by each WOA, which led us to uncover a core transcriptional response that was largely unrelated to other previously published C. albicans transcriptional stress responses. Genes commonly up-regulated by WOAs were enriched in several iron transporters, which was associated with an overall decrease in intracellular iron concentrations. Moreover, chronic exposure to any WOA lead to down-regulation of RNA synthesis and ribosome biogenesis genes, which resulted in significant reduction of total RNA levels and of ribosomal RNA in particular. In conclusion, this study suggests that gastrointestinal microbiota might directly influence C. albicans physiology via production of WOAs, with possible implications of how this fungus interacts with its host in both health and disease. Genetics Society of America 2015-01-29 /pmc/articles/PMC4390566/ /pubmed/25636313 http://dx.doi.org/10.1534/g3.114.015941 Text en Copyright © 2015 Cottier et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Cottier, Fabien
Tan, Alrina Shin Min
Chen, Jinmiao
Lum, Josephine
Zolezzi, Francesca
Poidinger, Michael
Pavelka, Norman
The Transcriptional Stress Response of Candida albicans to Weak Organic Acids
title The Transcriptional Stress Response of Candida albicans to Weak Organic Acids
title_full The Transcriptional Stress Response of Candida albicans to Weak Organic Acids
title_fullStr The Transcriptional Stress Response of Candida albicans to Weak Organic Acids
title_full_unstemmed The Transcriptional Stress Response of Candida albicans to Weak Organic Acids
title_short The Transcriptional Stress Response of Candida albicans to Weak Organic Acids
title_sort transcriptional stress response of candida albicans to weak organic acids
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390566/
https://www.ncbi.nlm.nih.gov/pubmed/25636313
http://dx.doi.org/10.1534/g3.114.015941
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