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Fungal zinc metabolism and its connections to virulence

Zinc is a ubiquitous metal in all life forms, as it is a structural component of the almost 10% of eukaryotic proteins, which are called zinc-binding proteins. In zinc-limiting conditions such as those found during infection, pathogenic fungi activate the expression of several systems to enhance the...

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Autores principales: Staats, Charley C., Kmetzsch, Lívia, Schrank, Augusto, Vainstein, Marilene H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3796257/
https://www.ncbi.nlm.nih.gov/pubmed/24133658
http://dx.doi.org/10.3389/fcimb.2013.00065
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author Staats, Charley C.
Kmetzsch, Lívia
Schrank, Augusto
Vainstein, Marilene H.
author_facet Staats, Charley C.
Kmetzsch, Lívia
Schrank, Augusto
Vainstein, Marilene H.
author_sort Staats, Charley C.
collection PubMed
description Zinc is a ubiquitous metal in all life forms, as it is a structural component of the almost 10% of eukaryotic proteins, which are called zinc-binding proteins. In zinc-limiting conditions such as those found during infection, pathogenic fungi activate the expression of several systems to enhance the uptake of zinc. These systems include ZIP transporters (solute carrier 39 family) and secreted zincophores, which are proteins that are able to chelate zinc. The expression of some fungal zinc uptake systems are regulated by a master regulator (Zap1), first characterized in the yeast Saccharomyces cerevisiae. In this review, we highlight features of zinc uptake and metabolism in human fungal pathogens and aspects of the relationship between proper zinc metabolism and the expression of virulence factors and adaptation to the host habitat.
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spelling pubmed-37962572013-10-16 Fungal zinc metabolism and its connections to virulence Staats, Charley C. Kmetzsch, Lívia Schrank, Augusto Vainstein, Marilene H. Front Cell Infect Microbiol Microbiology Zinc is a ubiquitous metal in all life forms, as it is a structural component of the almost 10% of eukaryotic proteins, which are called zinc-binding proteins. In zinc-limiting conditions such as those found during infection, pathogenic fungi activate the expression of several systems to enhance the uptake of zinc. These systems include ZIP transporters (solute carrier 39 family) and secreted zincophores, which are proteins that are able to chelate zinc. The expression of some fungal zinc uptake systems are regulated by a master regulator (Zap1), first characterized in the yeast Saccharomyces cerevisiae. In this review, we highlight features of zinc uptake and metabolism in human fungal pathogens and aspects of the relationship between proper zinc metabolism and the expression of virulence factors and adaptation to the host habitat. Frontiers Media S.A. 2013-10-14 /pmc/articles/PMC3796257/ /pubmed/24133658 http://dx.doi.org/10.3389/fcimb.2013.00065 Text en Copyright © 2013 Staats, Kmetzsch, Schrank and Vainstein. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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
Staats, Charley C.
Kmetzsch, Lívia
Schrank, Augusto
Vainstein, Marilene H.
Fungal zinc metabolism and its connections to virulence
title Fungal zinc metabolism and its connections to virulence
title_full Fungal zinc metabolism and its connections to virulence
title_fullStr Fungal zinc metabolism and its connections to virulence
title_full_unstemmed Fungal zinc metabolism and its connections to virulence
title_short Fungal zinc metabolism and its connections to virulence
title_sort fungal zinc metabolism and its connections to virulence
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3796257/
https://www.ncbi.nlm.nih.gov/pubmed/24133658
http://dx.doi.org/10.3389/fcimb.2013.00065
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