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Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis

Aspergillus fumigatus is a saprobic fungus that causes a range of pulmonary diseases, some of which are characterised by fungal persistence such as is observed in cystic fibrosis (CF) patients. Creation of genetic variation is critical for A. fumigatus to adapt to the lung environment, but biofilm f...

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Autores principales: Engel, Tobias, Verweij, Paul E., van den Heuvel, Joost, Wangmo, Dechen, Zhang, Jianhua, Debets, Alfons J.M., Snelders, Eveline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720686/
https://www.ncbi.nlm.nih.gov/pubmed/33313304
http://dx.doi.org/10.1183/23120541.00020-2020
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author Engel, Tobias
Verweij, Paul E.
van den Heuvel, Joost
Wangmo, Dechen
Zhang, Jianhua
Debets, Alfons J.M.
Snelders, Eveline
author_facet Engel, Tobias
Verweij, Paul E.
van den Heuvel, Joost
Wangmo, Dechen
Zhang, Jianhua
Debets, Alfons J.M.
Snelders, Eveline
author_sort Engel, Tobias
collection PubMed
description Aspergillus fumigatus is a saprobic fungus that causes a range of pulmonary diseases, some of which are characterised by fungal persistence such as is observed in cystic fibrosis (CF) patients. Creation of genetic variation is critical for A. fumigatus to adapt to the lung environment, but biofilm formation, especially in CF patients, may preclude mutational supply in A. fumigatus due to its confinement to the hyphal morphotype. We tested our hypothesis that genetic variation is created through parasexual recombination in chronic biofilms by phenotypic and genetic analysis of A. fumigatus isolates cultured from different origins. As diploids are the hallmark of parasex, we screened 799 A. fumigatus isolates obtained from patients with CF, chronic pulmonary lung disease and acute invasive aspergillosis, and from the environment for spore size. Benomyl sensitivity, nuclear content measurements through fluorescence-activated cell sorting and scanning electron microscopy were used to confirm the diploid state of large size spores. Whole genome sequencing was used to characterise diploid-associated genetic variation. We identified 11 diploids in isolates recovered from six of 11 (55%) CF patients and from one of 24 (4%) chronic aspergillosis patients, but not in 368 isolates from patients with acute Aspergillus infection and the environment. Diploid formation was associated with accumulation of mutations and variable haploid offspring including a voriconazole-resistant isolate. Parasexual recombination allows A. fumigatus to adapt and persist in CF patients, and plays a role in azole resistance development. Our findings are highly significant for understanding the genetics and biology of A. fumigatus in the human lung.
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spelling pubmed-77206862020-12-10 Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis Engel, Tobias Verweij, Paul E. van den Heuvel, Joost Wangmo, Dechen Zhang, Jianhua Debets, Alfons J.M. Snelders, Eveline ERJ Open Res Original Articles Aspergillus fumigatus is a saprobic fungus that causes a range of pulmonary diseases, some of which are characterised by fungal persistence such as is observed in cystic fibrosis (CF) patients. Creation of genetic variation is critical for A. fumigatus to adapt to the lung environment, but biofilm formation, especially in CF patients, may preclude mutational supply in A. fumigatus due to its confinement to the hyphal morphotype. We tested our hypothesis that genetic variation is created through parasexual recombination in chronic biofilms by phenotypic and genetic analysis of A. fumigatus isolates cultured from different origins. As diploids are the hallmark of parasex, we screened 799 A. fumigatus isolates obtained from patients with CF, chronic pulmonary lung disease and acute invasive aspergillosis, and from the environment for spore size. Benomyl sensitivity, nuclear content measurements through fluorescence-activated cell sorting and scanning electron microscopy were used to confirm the diploid state of large size spores. Whole genome sequencing was used to characterise diploid-associated genetic variation. We identified 11 diploids in isolates recovered from six of 11 (55%) CF patients and from one of 24 (4%) chronic aspergillosis patients, but not in 368 isolates from patients with acute Aspergillus infection and the environment. Diploid formation was associated with accumulation of mutations and variable haploid offspring including a voriconazole-resistant isolate. Parasexual recombination allows A. fumigatus to adapt and persist in CF patients, and plays a role in azole resistance development. Our findings are highly significant for understanding the genetics and biology of A. fumigatus in the human lung. European Respiratory Society 2020-12-07 /pmc/articles/PMC7720686/ /pubmed/33313304 http://dx.doi.org/10.1183/23120541.00020-2020 Text en Copyright ©ERS 2020 http://creativecommons.org/licenses/by-nc/4.0/This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
spellingShingle Original Articles
Engel, Tobias
Verweij, Paul E.
van den Heuvel, Joost
Wangmo, Dechen
Zhang, Jianhua
Debets, Alfons J.M.
Snelders, Eveline
Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis
title Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis
title_full Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis
title_fullStr Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis
title_full_unstemmed Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis
title_short Parasexual recombination enables Aspergillus fumigatus to persist in cystic fibrosis
title_sort parasexual recombination enables aspergillus fumigatus to persist in cystic fibrosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720686/
https://www.ncbi.nlm.nih.gov/pubmed/33313304
http://dx.doi.org/10.1183/23120541.00020-2020
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