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Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii
The Pacific Northwest outbreak of cryptococcosis, caused by a near-clonal lineage of the fungal pathogen Cryptococcus gattii, represents the most significant cluster of life-threatening fungal infections in otherwise healthy human hosts currently known. The outbreak lineage has a remarkable ability...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908794/ https://www.ncbi.nlm.nih.gov/pubmed/29674675 http://dx.doi.org/10.1038/s41467-018-03991-6 |
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author | Bielska, Ewa Sisquella, Marta Arch Aldeieg, Maha Birch, Charlotte O’Donoghue, Eloise J. May, Robin C. |
author_facet | Bielska, Ewa Sisquella, Marta Arch Aldeieg, Maha Birch, Charlotte O’Donoghue, Eloise J. May, Robin C. |
author_sort | Bielska, Ewa |
collection | PubMed |
description | The Pacific Northwest outbreak of cryptococcosis, caused by a near-clonal lineage of the fungal pathogen Cryptococcus gattii, represents the most significant cluster of life-threatening fungal infections in otherwise healthy human hosts currently known. The outbreak lineage has a remarkable ability to grow rapidly within human white blood cells, using a unique ‘division of labour’ mechanism within the pathogen population, where some cells adopt a dormant behaviour to support the growth of neighbouring cells. Here we demonstrate that pathogenic ‘division of labour’ can be triggered over large cellular distances and is mediated through the release of extracellular vesicles by the fungus. Isolated vesicles released by virulent strains are taken up by infected host macrophages and trafficked to the phagosome, where they trigger the rapid intracellular growth of non-outbreak fungal cells that would otherwise be eliminated by the host. Thus, long distance pathogen-to-pathogen communication via extracellular vesicles represents a novel mechanism to control complex virulence phenotypes in Cryptococcus gattii and, potentially, other infectious species. |
format | Online Article Text |
id | pubmed-5908794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59087942018-04-23 Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii Bielska, Ewa Sisquella, Marta Arch Aldeieg, Maha Birch, Charlotte O’Donoghue, Eloise J. May, Robin C. Nat Commun Article The Pacific Northwest outbreak of cryptococcosis, caused by a near-clonal lineage of the fungal pathogen Cryptococcus gattii, represents the most significant cluster of life-threatening fungal infections in otherwise healthy human hosts currently known. The outbreak lineage has a remarkable ability to grow rapidly within human white blood cells, using a unique ‘division of labour’ mechanism within the pathogen population, where some cells adopt a dormant behaviour to support the growth of neighbouring cells. Here we demonstrate that pathogenic ‘division of labour’ can be triggered over large cellular distances and is mediated through the release of extracellular vesicles by the fungus. Isolated vesicles released by virulent strains are taken up by infected host macrophages and trafficked to the phagosome, where they trigger the rapid intracellular growth of non-outbreak fungal cells that would otherwise be eliminated by the host. Thus, long distance pathogen-to-pathogen communication via extracellular vesicles represents a novel mechanism to control complex virulence phenotypes in Cryptococcus gattii and, potentially, other infectious species. Nature Publishing Group UK 2018-04-19 /pmc/articles/PMC5908794/ /pubmed/29674675 http://dx.doi.org/10.1038/s41467-018-03991-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bielska, Ewa Sisquella, Marta Arch Aldeieg, Maha Birch, Charlotte O’Donoghue, Eloise J. May, Robin C. Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii |
title | Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii |
title_full | Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii |
title_fullStr | Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii |
title_full_unstemmed | Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii |
title_short | Pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen Cryptococcus gattii |
title_sort | pathogen-derived extracellular vesicles mediate virulence in the fatal human pathogen cryptococcus gattii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908794/ https://www.ncbi.nlm.nih.gov/pubmed/29674675 http://dx.doi.org/10.1038/s41467-018-03991-6 |
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