Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.

Eukaryotic cells have evolved mechanisms to sense and adapt to dynamic environmental changes. Adaptation to thermal insults, in particular, is essential for their survival. The major fungal pathogen of humans, Candida albicans, is obligately associated with warm-blooded animals and hence occupies th...

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Main Authors: Michelle D Leach, Katarzyna M Tyc, Alistair J P Brown, Edda Klipp
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3308945?pdf=render
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spelling doaj-6849efee76b5472693640382fdf22bbd2020-11-25T00:51:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3246710.1371/journal.pone.0032467Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.Michelle D LeachKatarzyna M TycAlistair J P BrownEdda KlippEukaryotic cells have evolved mechanisms to sense and adapt to dynamic environmental changes. Adaptation to thermal insults, in particular, is essential for their survival. The major fungal pathogen of humans, Candida albicans, is obligately associated with warm-blooded animals and hence occupies thermally buffered niches. Yet during its evolution in the host it has retained a bona fide heat shock response whilst other stress responses have diverged significantly. Furthermore the heat shock response is essential for the virulence of C. albicans. With a view to understanding the relevance of this response to infection we have explored the dynamic regulation of thermal adaptation using an integrative systems biology approach. Our mathematical model of thermal regulation, which has been validated experimentally in C. albicans, describes the dynamic autoregulation of the heat shock transcription factor Hsf1 and the essential chaperone protein Hsp90. We have used this model to show that the thermal adaptation system displays perfect adaptation, that it retains a transient molecular memory, and that Hsf1 is activated during thermal transitions that mimic fever. In addition to providing explanations for the evolutionary conservation of the heat shock response in this pathogen and the relevant of this response to infection, our model provides a platform for the analysis of thermal adaptation in other eukaryotic cells.http://europepmc.org/articles/PMC3308945?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Michelle D Leach
Katarzyna M Tyc
Alistair J P Brown
Edda Klipp
spellingShingle Michelle D Leach
Katarzyna M Tyc
Alistair J P Brown
Edda Klipp
Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.
PLoS ONE
author_facet Michelle D Leach
Katarzyna M Tyc
Alistair J P Brown
Edda Klipp
author_sort Michelle D Leach
title Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.
title_short Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.
title_full Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.
title_fullStr Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.
title_full_unstemmed Modelling the regulation of thermal adaptation in Candida albicans, a major fungal pathogen of humans.
title_sort modelling the regulation of thermal adaptation in candida albicans, a major fungal pathogen of humans.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Eukaryotic cells have evolved mechanisms to sense and adapt to dynamic environmental changes. Adaptation to thermal insults, in particular, is essential for their survival. The major fungal pathogen of humans, Candida albicans, is obligately associated with warm-blooded animals and hence occupies thermally buffered niches. Yet during its evolution in the host it has retained a bona fide heat shock response whilst other stress responses have diverged significantly. Furthermore the heat shock response is essential for the virulence of C. albicans. With a view to understanding the relevance of this response to infection we have explored the dynamic regulation of thermal adaptation using an integrative systems biology approach. Our mathematical model of thermal regulation, which has been validated experimentally in C. albicans, describes the dynamic autoregulation of the heat shock transcription factor Hsf1 and the essential chaperone protein Hsp90. We have used this model to show that the thermal adaptation system displays perfect adaptation, that it retains a transient molecular memory, and that Hsf1 is activated during thermal transitions that mimic fever. In addition to providing explanations for the evolutionary conservation of the heat shock response in this pathogen and the relevant of this response to infection, our model provides a platform for the analysis of thermal adaptation in other eukaryotic cells.
url http://europepmc.org/articles/PMC3308945?pdf=render
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