Grf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>

ABSTRACT Candida albicans is an opportunistic human fungal pathogen that causes superficial fungal infections and lethal systemic infections. To colonize and establish infections, C. albicans coordinates the expression of virulence and metabolic genes. Previous work showed that the homeodomain trans...

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Autores principales: Tanaporn Wangsanut, Anup K. Ghosh, Peter G. Metzger, William A. Fonzi, Ronda J. Rolfes
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Publicado: American Society for Microbiology 2017
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spelling oai:doaj.org-article:474d36707be44f49b1816c40fa82c9262021-11-15T15:22:04ZGrf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>10.1128/mSphere.00161-172379-5042https://doaj.org/article/474d36707be44f49b1816c40fa82c9262017-08-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00161-17https://doaj.org/toc/2379-5042ABSTRACT Candida albicans is an opportunistic human fungal pathogen that causes superficial fungal infections and lethal systemic infections. To colonize and establish infections, C. albicans coordinates the expression of virulence and metabolic genes. Previous work showed that the homeodomain transcription factor Grf10 is required for formation of hyphae, a virulence factor. Here we report global gene expression analysis of a grf10Δ strain using a DNA microarray and identify genes for de novo adenylate biosynthesis (ADE genes), one-carbon metabolism, and a nucleoside permease (NUP). Upregulation of these genes in response to adenine limitation required both Grf10 and the myb protein Bas1, as shown by quantitative real-time PCR (qRT-PCR). Phenotypic analysis showed that both mutants exhibited growth defects when grown in the absence of adenine, and the doubling time was slower for the bas1Δ mutant. Bas1 is required for basal expression of these genes, whereas NUP expression is more dependent upon Grf10. Disruption of BAS1 led to only modest defects in hypha formation and weak attenuation of virulence in a systemic mouse model of infection, as opposed to the previously reported strong effects found in the grf10Δ mutant. Our data are consistent with a model in which Grf10 coordinates metabolic effects on nucleotide metabolism by interaction with Bas1 and indicate that AMP biosynthesis and its regulation are important for C. albicans growth and virulence. IMPORTANCE Candida albicans is a commensal and a common constituent of the human microbiota; however, it can become pathogenic and cause infections in both immunocompetent and immunocompromised people. C. albicans exhibits remarkable metabolic versatility as it can colonize multiple body sites as a commensal or pathogen. Understanding how C. albicans adapts metabolically to each ecological niche is essential for developing novel therapeutic approaches. Purine metabolism has been targeted pharmaceutically in several diseases; however, the regulation of this pathway has not been fully elucidated in C. albicans. Here, we report how C. albicans controls the AMP de novo biosynthesis pathway in response to purine availability. We show that the lack of the transcription factors Grf10 and Bas1 leads to purine metabolic dysfunction, and this dysfunction affects the ability of C. albicans to establish infections.Tanaporn WangsanutAnup K. GhoshPeter G. MetzgerWilliam A. FonziRonda J. RolfesAmerican Society for MicrobiologyarticleBas1Candida albicansGrf10fungal pathogenone-carbon metabolismpurine metabolismMicrobiologyQR1-502ENmSphere, Vol 2, Iss 4 (2017)
institution DOAJ
collection DOAJ
language EN
topic Bas1
Candida albicans
Grf10
fungal pathogen
one-carbon metabolism
purine metabolism
Microbiology
QR1-502
spellingShingle Bas1
Candida albicans
Grf10
fungal pathogen
one-carbon metabolism
purine metabolism
Microbiology
QR1-502
Tanaporn Wangsanut
Anup K. Ghosh
Peter G. Metzger
William A. Fonzi
Ronda J. Rolfes
Grf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>
description ABSTRACT Candida albicans is an opportunistic human fungal pathogen that causes superficial fungal infections and lethal systemic infections. To colonize and establish infections, C. albicans coordinates the expression of virulence and metabolic genes. Previous work showed that the homeodomain transcription factor Grf10 is required for formation of hyphae, a virulence factor. Here we report global gene expression analysis of a grf10Δ strain using a DNA microarray and identify genes for de novo adenylate biosynthesis (ADE genes), one-carbon metabolism, and a nucleoside permease (NUP). Upregulation of these genes in response to adenine limitation required both Grf10 and the myb protein Bas1, as shown by quantitative real-time PCR (qRT-PCR). Phenotypic analysis showed that both mutants exhibited growth defects when grown in the absence of adenine, and the doubling time was slower for the bas1Δ mutant. Bas1 is required for basal expression of these genes, whereas NUP expression is more dependent upon Grf10. Disruption of BAS1 led to only modest defects in hypha formation and weak attenuation of virulence in a systemic mouse model of infection, as opposed to the previously reported strong effects found in the grf10Δ mutant. Our data are consistent with a model in which Grf10 coordinates metabolic effects on nucleotide metabolism by interaction with Bas1 and indicate that AMP biosynthesis and its regulation are important for C. albicans growth and virulence. IMPORTANCE Candida albicans is a commensal and a common constituent of the human microbiota; however, it can become pathogenic and cause infections in both immunocompetent and immunocompromised people. C. albicans exhibits remarkable metabolic versatility as it can colonize multiple body sites as a commensal or pathogen. Understanding how C. albicans adapts metabolically to each ecological niche is essential for developing novel therapeutic approaches. Purine metabolism has been targeted pharmaceutically in several diseases; however, the regulation of this pathway has not been fully elucidated in C. albicans. Here, we report how C. albicans controls the AMP de novo biosynthesis pathway in response to purine availability. We show that the lack of the transcription factors Grf10 and Bas1 leads to purine metabolic dysfunction, and this dysfunction affects the ability of C. albicans to establish infections.
format article
author Tanaporn Wangsanut
Anup K. Ghosh
Peter G. Metzger
William A. Fonzi
Ronda J. Rolfes
author_facet Tanaporn Wangsanut
Anup K. Ghosh
Peter G. Metzger
William A. Fonzi
Ronda J. Rolfes
author_sort Tanaporn Wangsanut
title Grf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>
title_short Grf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>
title_full Grf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>
title_fullStr Grf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>
title_full_unstemmed Grf10 and Bas1 Regulate Transcription of Adenylate and One-Carbon Biosynthesis Genes and Affect Virulence in the Human Fungal Pathogen <named-content content-type="genus-species">Candida albicans</named-content>
title_sort grf10 and bas1 regulate transcription of adenylate and one-carbon biosynthesis genes and affect virulence in the human fungal pathogen <named-content content-type="genus-species">candida albicans</named-content>
publisher American Society for Microbiology
publishDate 2017
url https://doaj.org/article/474d36707be44f49b1816c40fa82c926
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