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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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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. |
format | Online Article Text |
id | pubmed-4208095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
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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