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Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation

Candida albicans occupies diverse ecological niches within the host and must tolerate a wide range of environmental pH. The plasma membrane H(+)-ATPase Pma1p is the major regulator of cytosolic pH in fungi. Pma1p extrudes protons from the cytosol to maintain neutral-to-alkaline pH and is a potential...

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Autores principales: Rane, Hallie S., Hayek, Summer R., Frye, Jillian E., Abeyta, Esteban L., Bernardo, Stella M., Parra, Karlett J., Lee, Samuel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521590/
https://www.ncbi.nlm.nih.gov/pubmed/31143168
http://dx.doi.org/10.3389/fmicb.2019.01012
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author Rane, Hallie S.
Hayek, Summer R.
Frye, Jillian E.
Abeyta, Esteban L.
Bernardo, Stella M.
Parra, Karlett J.
Lee, Samuel A.
author_facet Rane, Hallie S.
Hayek, Summer R.
Frye, Jillian E.
Abeyta, Esteban L.
Bernardo, Stella M.
Parra, Karlett J.
Lee, Samuel A.
author_sort Rane, Hallie S.
collection PubMed
description Candida albicans occupies diverse ecological niches within the host and must tolerate a wide range of environmental pH. The plasma membrane H(+)-ATPase Pma1p is the major regulator of cytosolic pH in fungi. Pma1p extrudes protons from the cytosol to maintain neutral-to-alkaline pH and is a potential drug target due to its essentiality and fungal specificity. We characterized mutants in which one allele of PMA1 has been deleted and the other truncated by 18–38 amino acids. Increasing C-terminal truncation caused corresponding decreases in plasma membrane ATPase-specific activity and cytosolic pH. Pma1p is regulated by glucose: glucose rapidly activates the ATPase, causing a sharp increase in cytosolic pH. Increasing Pma1p truncation severely impaired this glucose response. Pma1p truncation also altered cation responses, disrupted vacuolar morphology and pH, and reduced filamentation competence. Early studies of cytosolic pH and filamentation have described a rapid, transient alkalinization of the cytosol preceding germ tube formation; Pma1p has been proposed as a regulator of this process. We find Pma1p plays a role in the establishment of cell polarity, and distribution of Pma1p is non-homogenous in emerging hyphae. These findings suggest a role of PMA1 in cytosolic alkalinization and in the specialized form of polarized growth that is filamentation.
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spelling pubmed-65215902019-05-29 Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation Rane, Hallie S. Hayek, Summer R. Frye, Jillian E. Abeyta, Esteban L. Bernardo, Stella M. Parra, Karlett J. Lee, Samuel A. Front Microbiol Microbiology Candida albicans occupies diverse ecological niches within the host and must tolerate a wide range of environmental pH. The plasma membrane H(+)-ATPase Pma1p is the major regulator of cytosolic pH in fungi. Pma1p extrudes protons from the cytosol to maintain neutral-to-alkaline pH and is a potential drug target due to its essentiality and fungal specificity. We characterized mutants in which one allele of PMA1 has been deleted and the other truncated by 18–38 amino acids. Increasing C-terminal truncation caused corresponding decreases in plasma membrane ATPase-specific activity and cytosolic pH. Pma1p is regulated by glucose: glucose rapidly activates the ATPase, causing a sharp increase in cytosolic pH. Increasing Pma1p truncation severely impaired this glucose response. Pma1p truncation also altered cation responses, disrupted vacuolar morphology and pH, and reduced filamentation competence. Early studies of cytosolic pH and filamentation have described a rapid, transient alkalinization of the cytosol preceding germ tube formation; Pma1p has been proposed as a regulator of this process. We find Pma1p plays a role in the establishment of cell polarity, and distribution of Pma1p is non-homogenous in emerging hyphae. These findings suggest a role of PMA1 in cytosolic alkalinization and in the specialized form of polarized growth that is filamentation. Frontiers Media S.A. 2019-05-09 /pmc/articles/PMC6521590/ /pubmed/31143168 http://dx.doi.org/10.3389/fmicb.2019.01012 Text en Copyright © 2019 Rane, Hayek, Frye, Abeyta, Bernardo, Parra and Lee. 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
Rane, Hallie S.
Hayek, Summer R.
Frye, Jillian E.
Abeyta, Esteban L.
Bernardo, Stella M.
Parra, Karlett J.
Lee, Samuel A.
Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation
title Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation
title_full Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation
title_fullStr Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation
title_full_unstemmed Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation
title_short Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation
title_sort candida albicans pma1p contributes to growth, ph homeostasis, and hyphal formation
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521590/
https://www.ncbi.nlm.nih.gov/pubmed/31143168
http://dx.doi.org/10.3389/fmicb.2019.01012
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