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Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition

Candida albicans is able to proliferate in environments that vary dramatically in ambient pH, a trait required for colonising niches such as the stomach, vaginal mucosal and the GI tract. Here we show that growth in acidic environments involves cell wall remodelling which results in enhanced chitin...

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Autores principales: Sherrington, Sarah L., Sorsby, Eleanor, Mahtey, Nabeel, Kumwenda, Pizga, Lenardon, Megan D., Brown, Ian, Ballou, Elizabeth R., MacCallum, Donna M., Hall, Rebecca A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456412/
https://www.ncbi.nlm.nih.gov/pubmed/28542528
http://dx.doi.org/10.1371/journal.ppat.1006403
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author Sherrington, Sarah L.
Sorsby, Eleanor
Mahtey, Nabeel
Kumwenda, Pizga
Lenardon, Megan D.
Brown, Ian
Ballou, Elizabeth R.
MacCallum, Donna M.
Hall, Rebecca A.
author_facet Sherrington, Sarah L.
Sorsby, Eleanor
Mahtey, Nabeel
Kumwenda, Pizga
Lenardon, Megan D.
Brown, Ian
Ballou, Elizabeth R.
MacCallum, Donna M.
Hall, Rebecca A.
author_sort Sherrington, Sarah L.
collection PubMed
description Candida albicans is able to proliferate in environments that vary dramatically in ambient pH, a trait required for colonising niches such as the stomach, vaginal mucosal and the GI tract. Here we show that growth in acidic environments involves cell wall remodelling which results in enhanced chitin and β-glucan exposure at the cell wall periphery. Unmasking of the underlying immuno-stimulatory β-glucan in acidic environments enhanced innate immune recognition of C. albicans by macrophages and neutrophils, and induced a stronger proinflammatory cytokine response, driven through the C-type lectin-like receptor, Dectin-1. This enhanced inflammatory response resulted in significant recruitment of neutrophils in an intraperitoneal model of infection, a hallmark of symptomatic vaginal colonisation. Enhanced chitin exposure resulted from reduced expression of the cell wall chitinase Cht2, via a Bcr1-Rim101 dependent signalling cascade, while increased β-glucan exposure was regulated via a non-canonical signalling pathway. We propose that this “unmasking” of the cell wall may induce non-protective hyper activation of the immune system during growth in acidic niches, and may attribute to symptomatic vaginal infection.
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spelling pubmed-54564122017-06-06 Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition Sherrington, Sarah L. Sorsby, Eleanor Mahtey, Nabeel Kumwenda, Pizga Lenardon, Megan D. Brown, Ian Ballou, Elizabeth R. MacCallum, Donna M. Hall, Rebecca A. PLoS Pathog Research Article Candida albicans is able to proliferate in environments that vary dramatically in ambient pH, a trait required for colonising niches such as the stomach, vaginal mucosal and the GI tract. Here we show that growth in acidic environments involves cell wall remodelling which results in enhanced chitin and β-glucan exposure at the cell wall periphery. Unmasking of the underlying immuno-stimulatory β-glucan in acidic environments enhanced innate immune recognition of C. albicans by macrophages and neutrophils, and induced a stronger proinflammatory cytokine response, driven through the C-type lectin-like receptor, Dectin-1. This enhanced inflammatory response resulted in significant recruitment of neutrophils in an intraperitoneal model of infection, a hallmark of symptomatic vaginal colonisation. Enhanced chitin exposure resulted from reduced expression of the cell wall chitinase Cht2, via a Bcr1-Rim101 dependent signalling cascade, while increased β-glucan exposure was regulated via a non-canonical signalling pathway. We propose that this “unmasking” of the cell wall may induce non-protective hyper activation of the immune system during growth in acidic niches, and may attribute to symptomatic vaginal infection. Public Library of Science 2017-05-22 /pmc/articles/PMC5456412/ /pubmed/28542528 http://dx.doi.org/10.1371/journal.ppat.1006403 Text en © 2017 Sherrington 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
Sherrington, Sarah L.
Sorsby, Eleanor
Mahtey, Nabeel
Kumwenda, Pizga
Lenardon, Megan D.
Brown, Ian
Ballou, Elizabeth R.
MacCallum, Donna M.
Hall, Rebecca A.
Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition
title Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition
title_full Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition
title_fullStr Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition
title_full_unstemmed Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition
title_short Adaptation of Candida albicans to environmental pH induces cell wall remodelling and enhances innate immune recognition
title_sort adaptation of candida albicans to environmental ph induces cell wall remodelling and enhances innate immune recognition
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456412/
https://www.ncbi.nlm.nih.gov/pubmed/28542528
http://dx.doi.org/10.1371/journal.ppat.1006403
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