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‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak

Cryptococcus gattii is an emerging intracellular pathogen and the cause of the largest primary outbreak of a life-threatening fungal disease in a healthy population. Outbreak strains share a unique mitochondrial gene expression profile and an increased ability to tubularize their mitochondria within...

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Autores principales: Voelz, Kerstin, Johnston, Simon A., Smith, Leanne M., Hall, Rebecca A., Idnurm, Alexander, May, Robin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208095/
https://www.ncbi.nlm.nih.gov/pubmed/25323068
http://dx.doi.org/10.1038/ncomms6194
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author Voelz, Kerstin
Johnston, Simon A.
Smith, Leanne M.
Hall, Rebecca A.
Idnurm, Alexander
May, Robin C.
author_facet Voelz, Kerstin
Johnston, Simon A.
Smith, Leanne M.
Hall, Rebecca A.
Idnurm, Alexander
May, Robin C.
author_sort Voelz, Kerstin
collection PubMed
description Cryptococcus gattii is an emerging intracellular pathogen and the cause of the largest primary outbreak of a life-threatening fungal disease in a healthy population. Outbreak strains share a unique mitochondrial gene expression profile and an increased ability to tubularize their mitochondria within host macrophages. However, the underlying mechanism that causes this lineage of C. gattii to be virulent in immunocompetent individuals remains unexplained. Here we show that a subpopulation of intracellular C. gattii adopts a tubular mitochondrial morphology in response to host reactive oxygen species. These fungal cells then facilitate the rapid growth of neighbouring C. gattii cells with non-tubular mitochondria, allowing for effective establishment of the pathogen within a macrophage intracellular niche. Thus, host reactive oxygen species, an essential component of the innate immune response, act as major signalling molecules to trigger a ‘division of labour’ in the intracellular fungal population, leading to increased pathogenesis within this outbreak lineage.
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spelling pubmed-42080952014-11-06 ‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak Voelz, Kerstin Johnston, Simon A. Smith, Leanne M. Hall, Rebecca A. Idnurm, Alexander May, Robin C. Nat Commun Article Cryptococcus gattii is an emerging intracellular pathogen and the cause of the largest primary outbreak of a life-threatening fungal disease in a healthy population. Outbreak strains share a unique mitochondrial gene expression profile and an increased ability to tubularize their mitochondria within host macrophages. However, the underlying mechanism that causes this lineage of C. gattii to be virulent in immunocompetent individuals remains unexplained. Here we show that a subpopulation of intracellular C. gattii adopts a tubular mitochondrial morphology in response to host reactive oxygen species. These fungal cells then facilitate the rapid growth of neighbouring C. gattii cells with non-tubular mitochondria, allowing for effective establishment of the pathogen within a macrophage intracellular niche. Thus, host reactive oxygen species, an essential component of the innate immune response, act as major signalling molecules to trigger a ‘division of labour’ in the intracellular fungal population, leading to increased pathogenesis within this outbreak lineage. Nature Pub. Group 2014-10-17 /pmc/articles/PMC4208095/ /pubmed/25323068 http://dx.doi.org/10.1038/ncomms6194 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Voelz, Kerstin
Johnston, Simon A.
Smith, Leanne M.
Hall, Rebecca A.
Idnurm, Alexander
May, Robin C.
‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak
title ‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak
title_full ‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak
title_fullStr ‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak
title_full_unstemmed ‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak
title_short ‘Division of labour’ in response to host oxidative burst drives a fatal Cryptococcus gattii outbreak
title_sort ‘division of labour’ in response to host oxidative burst drives a fatal cryptococcus gattii outbreak
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208095/
https://www.ncbi.nlm.nih.gov/pubmed/25323068
http://dx.doi.org/10.1038/ncomms6194
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