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Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans

This study explored the antifungal potential of perillyl alcohol (PA), a natural monoterpene alcohol, against most prevalent human fungal pathogen C. albicans, its clinical isolates and four non-albicans species of Candida. To resolve the potential mechanisms, we used whole genome transcriptome anal...

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Autores principales: Ansari, Moiz A., Fatima, Zeeshan, Hameed, Saif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023166/
https://www.ncbi.nlm.nih.gov/pubmed/27627759
http://dx.doi.org/10.1371/journal.pone.0162465
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author Ansari, Moiz A.
Fatima, Zeeshan
Hameed, Saif
author_facet Ansari, Moiz A.
Fatima, Zeeshan
Hameed, Saif
author_sort Ansari, Moiz A.
collection PubMed
description This study explored the antifungal potential of perillyl alcohol (PA), a natural monoterpene alcohol, against most prevalent human fungal pathogen C. albicans, its clinical isolates and four non-albicans species of Candida. To resolve the potential mechanisms, we used whole genome transcriptome analyses of PA treated Candida cells to examine the affected cellular circuitry of this pathogen. The transcriptome data revealed a link between calcineurin signaling and PA as among the several categories of PA responsive genes the down regulation of calcineurin signaling gene CNB1 was noteworthy which was also confirmed by both molecular docking and susceptibility assays. We observed that PA treated Candida phenocopied compromised calcineurin pathway stress responses and turned sensitive to alkaline pH, ionic, membrane, salinity, endoplasmic reticulum and serum stresses. Indispensability of functional calcineurin was further confirmed as calcineurin mutant was hypersensitive to PA while constitutively expressed calcineurin strain remained resistant. We explored that PA leads to perturbed membrane integrity as depicted through depleted ergosterol levels and disrupted pH homeostasis. Moreover, PA caused cell wall damage which was evident from hypersensitivity against cell wall perturbing agents (congo red, calcoflour white), SEM and enhanced rate of cell sedimentation. Furthermore, PA inhibited potential virulence traits including morphological transition, biofilm formation and displayed diminished capacity to adhere both to the polystyrene surface and buccal epithelial cells. The study also revealed that PA leads to cell cycle arrest and mitochondrial dysfunction in C. albicans. Together, the present study provides enough evidence for further work on PA so that better strategies could be employed to treat Candida infections.
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spelling pubmed-50231662016-09-27 Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans Ansari, Moiz A. Fatima, Zeeshan Hameed, Saif PLoS One Research Article This study explored the antifungal potential of perillyl alcohol (PA), a natural monoterpene alcohol, against most prevalent human fungal pathogen C. albicans, its clinical isolates and four non-albicans species of Candida. To resolve the potential mechanisms, we used whole genome transcriptome analyses of PA treated Candida cells to examine the affected cellular circuitry of this pathogen. The transcriptome data revealed a link between calcineurin signaling and PA as among the several categories of PA responsive genes the down regulation of calcineurin signaling gene CNB1 was noteworthy which was also confirmed by both molecular docking and susceptibility assays. We observed that PA treated Candida phenocopied compromised calcineurin pathway stress responses and turned sensitive to alkaline pH, ionic, membrane, salinity, endoplasmic reticulum and serum stresses. Indispensability of functional calcineurin was further confirmed as calcineurin mutant was hypersensitive to PA while constitutively expressed calcineurin strain remained resistant. We explored that PA leads to perturbed membrane integrity as depicted through depleted ergosterol levels and disrupted pH homeostasis. Moreover, PA caused cell wall damage which was evident from hypersensitivity against cell wall perturbing agents (congo red, calcoflour white), SEM and enhanced rate of cell sedimentation. Furthermore, PA inhibited potential virulence traits including morphological transition, biofilm formation and displayed diminished capacity to adhere both to the polystyrene surface and buccal epithelial cells. The study also revealed that PA leads to cell cycle arrest and mitochondrial dysfunction in C. albicans. Together, the present study provides enough evidence for further work on PA so that better strategies could be employed to treat Candida infections. Public Library of Science 2016-09-14 /pmc/articles/PMC5023166/ /pubmed/27627759 http://dx.doi.org/10.1371/journal.pone.0162465 Text en © 2016 Ansari et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ansari, Moiz A.
Fatima, Zeeshan
Hameed, Saif
Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
title Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
title_full Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
title_fullStr Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
title_full_unstemmed Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
title_short Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
title_sort anticandidal effect and mechanisms of monoterpenoid, perillyl alcohol against candida albicans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023166/
https://www.ncbi.nlm.nih.gov/pubmed/27627759
http://dx.doi.org/10.1371/journal.pone.0162465
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