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Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans

BACKGROUND: Ten secreted aspartyl proteinase (Sap) genes were identified in Candida albicans. The products of SAP genes are considered to be virulent factors of C. albicans that participated in causing mucocutaneous and systemic candidiasis in humans. Depending on environmental conditions, C. albica...

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Autores principales: Buu, Leh-Miauh, Chen, Yee-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995546/
https://www.ncbi.nlm.nih.gov/pubmed/24628998
http://dx.doi.org/10.1186/1423-0127-21-22
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author Buu, Leh-Miauh
Chen, Yee-Chun
author_facet Buu, Leh-Miauh
Chen, Yee-Chun
author_sort Buu, Leh-Miauh
collection PubMed
description BACKGROUND: Ten secreted aspartyl proteinase (Sap) genes were identified in Candida albicans. The products of SAP genes are considered to be virulent factors of C. albicans that participated in causing mucocutaneous and systemic candidiasis in humans. Depending on environmental conditions, C. albicans may stay in yeast-form or convert into invasive hypha-form, and these issues may affect the expression of SAP genes. In this study we explored the component(s) of culture media that may affect the expression of hypha-associated SAP genes. RESULTS: We demonstrate that glucose levels modulate both the hyphae development and the expression strength of hypha-associated SAP genes (SAP4-6). In contrast to high glucose concentration (2%), lower glucose level (0.1%) is more potent to promote hyphae development and to promptly elicit the expression of hypha-associated Sap proteins during yeast-to-hypha transition of C. albicans. Both Cph1-mediated MAP kinase cascade and Efg1-mediated cAMP/PKA pathway, although the latter seemed dominant, participate in convey the glucose signaling to regulate the expression of hypha-associated SAP genes and this glucose level effect may perform at very early stage of yeast-to-hypha transition. In addition, when C. albicans was co-cultured with THP-1 human monocytes, the engulfed C. albicans was developing hypha efficiently within 1 hr and the expression of hypha-associated Sap proteins could be detected on the distal surface of hyphae. CONCLUSION: We propose that the glucose level of bloodstream (approximately 0.1%) may be facilitated for stimulation of C. albicans to develop invasive hypha-form and to elicit promptly production of high-level hypha-associated Sap proteins.
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spelling pubmed-39955462014-04-23 Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans Buu, Leh-Miauh Chen, Yee-Chun J Biomed Sci Research BACKGROUND: Ten secreted aspartyl proteinase (Sap) genes were identified in Candida albicans. The products of SAP genes are considered to be virulent factors of C. albicans that participated in causing mucocutaneous and systemic candidiasis in humans. Depending on environmental conditions, C. albicans may stay in yeast-form or convert into invasive hypha-form, and these issues may affect the expression of SAP genes. In this study we explored the component(s) of culture media that may affect the expression of hypha-associated SAP genes. RESULTS: We demonstrate that glucose levels modulate both the hyphae development and the expression strength of hypha-associated SAP genes (SAP4-6). In contrast to high glucose concentration (2%), lower glucose level (0.1%) is more potent to promote hyphae development and to promptly elicit the expression of hypha-associated Sap proteins during yeast-to-hypha transition of C. albicans. Both Cph1-mediated MAP kinase cascade and Efg1-mediated cAMP/PKA pathway, although the latter seemed dominant, participate in convey the glucose signaling to regulate the expression of hypha-associated SAP genes and this glucose level effect may perform at very early stage of yeast-to-hypha transition. In addition, when C. albicans was co-cultured with THP-1 human monocytes, the engulfed C. albicans was developing hypha efficiently within 1 hr and the expression of hypha-associated Sap proteins could be detected on the distal surface of hyphae. CONCLUSION: We propose that the glucose level of bloodstream (approximately 0.1%) may be facilitated for stimulation of C. albicans to develop invasive hypha-form and to elicit promptly production of high-level hypha-associated Sap proteins. BioMed Central 2014-03-15 /pmc/articles/PMC3995546/ /pubmed/24628998 http://dx.doi.org/10.1186/1423-0127-21-22 Text en Copyright © 2014 Buu and Chen; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Buu, Leh-Miauh
Chen, Yee-Chun
Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans
title Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans
title_full Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans
title_fullStr Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans
title_full_unstemmed Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans
title_short Impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in Candida albicans
title_sort impact of glucose levels on expression of hypha-associated secreted aspartyl proteinases in candida albicans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995546/
https://www.ncbi.nlm.nih.gov/pubmed/24628998
http://dx.doi.org/10.1186/1423-0127-21-22
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