Cargando…
Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans
Copper homeostasis is an important determinant for virulence of many human pathogenic fungi such as the highly prevalent yeast Candida albicans. However, beyond the copper transporter Ctr1, little is known regarding other genes and biological processes that are affected by copper. To gain insight in...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248230/ https://www.ncbi.nlm.nih.gov/pubmed/32508775 http://dx.doi.org/10.3389/fmicb.2020.00935 |
_version_ | 1783538324489633792 |
---|---|
author | Khemiri, Inès Tebbji, Faiza Sellam, Adnane |
author_facet | Khemiri, Inès Tebbji, Faiza Sellam, Adnane |
author_sort | Khemiri, Inès |
collection | PubMed |
description | Copper homeostasis is an important determinant for virulence of many human pathogenic fungi such as the highly prevalent yeast Candida albicans. However, beyond the copper transporter Ctr1, little is known regarding other genes and biological processes that are affected by copper. To gain insight into the cellular processes that are modulated by copper abundance in C. albicans, we monitored the global gene expression dynamic under both copper depletion and excess using RNA-seq. Beyond copper metabolism, other different transcriptional programs related to fungal fitness such as stress responses, antifungal sensitivity, host invasion and commensalism were modulated in response to copper variations. We have also investigated the transcriptome of the mutant of the copper utilization regulator, mac1, and identified potential direct targets of this transcription factor under copper starvation. We also showed that Mac1 was required for the invasion and adhesion to host cells and antifungal tolerance. This study provides a framework for future studies to examine the link between copper metabolism and essential functions that modulate fungal virulence and fitness inside the host. |
format | Online Article Text |
id | pubmed-7248230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72482302020-06-05 Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans Khemiri, Inès Tebbji, Faiza Sellam, Adnane Front Microbiol Microbiology Copper homeostasis is an important determinant for virulence of many human pathogenic fungi such as the highly prevalent yeast Candida albicans. However, beyond the copper transporter Ctr1, little is known regarding other genes and biological processes that are affected by copper. To gain insight into the cellular processes that are modulated by copper abundance in C. albicans, we monitored the global gene expression dynamic under both copper depletion and excess using RNA-seq. Beyond copper metabolism, other different transcriptional programs related to fungal fitness such as stress responses, antifungal sensitivity, host invasion and commensalism were modulated in response to copper variations. We have also investigated the transcriptome of the mutant of the copper utilization regulator, mac1, and identified potential direct targets of this transcription factor under copper starvation. We also showed that Mac1 was required for the invasion and adhesion to host cells and antifungal tolerance. This study provides a framework for future studies to examine the link between copper metabolism and essential functions that modulate fungal virulence and fitness inside the host. Frontiers Media S.A. 2020-05-19 /pmc/articles/PMC7248230/ /pubmed/32508775 http://dx.doi.org/10.3389/fmicb.2020.00935 Text en Copyright © 2020 Khemiri, Tebbji and Sellam. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Khemiri, Inès Tebbji, Faiza Sellam, Adnane Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans |
title | Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans |
title_full | Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans |
title_fullStr | Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans |
title_full_unstemmed | Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans |
title_short | Transcriptome Analysis Uncovers a Link Between Copper Metabolism, and Both Fungal Fitness and Antifungal Sensitivity in the Opportunistic Yeast Candida albicans |
title_sort | transcriptome analysis uncovers a link between copper metabolism, and both fungal fitness and antifungal sensitivity in the opportunistic yeast candida albicans |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248230/ https://www.ncbi.nlm.nih.gov/pubmed/32508775 http://dx.doi.org/10.3389/fmicb.2020.00935 |
work_keys_str_mv | AT khemiriines transcriptomeanalysisuncoversalinkbetweencoppermetabolismandbothfungalfitnessandantifungalsensitivityintheopportunisticyeastcandidaalbicans AT tebbjifaiza transcriptomeanalysisuncoversalinkbetweencoppermetabolismandbothfungalfitnessandantifungalsensitivityintheopportunisticyeastcandidaalbicans AT sellamadnane transcriptomeanalysisuncoversalinkbetweencoppermetabolismandbothfungalfitnessandantifungalsensitivityintheopportunisticyeastcandidaalbicans |