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The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection
The phenotypic plasticity of Cryptococcus neoformans is widely studied and demonstrated in vitro, but its influence on pathogenicity remains unclear. In this study, we investigated the dynamics of cryptococcal cell and transcriptional remodeling during pulmonary infection in a murine model. We showe...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740611/ https://www.ncbi.nlm.nih.gov/pubmed/36497155 http://dx.doi.org/10.3390/cells11233896 |
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author | Freitas, Gustavo J. C. Gouveia-Eufrasio, Ludmila Emidio, Eluzia C. P. Carneiro, Hellem C. S. de Matos Baltazar, Ludmila Costa, Marliete C. Frases, Susana de Sousa Araújo, Glauber R. Paixão, Tatiane A. Sossai, Brunno G. Caza, Melissa Kronstad, James W. Peres, Nalu T. A. Santos, Daniel A. |
author_facet | Freitas, Gustavo J. C. Gouveia-Eufrasio, Ludmila Emidio, Eluzia C. P. Carneiro, Hellem C. S. de Matos Baltazar, Ludmila Costa, Marliete C. Frases, Susana de Sousa Araújo, Glauber R. Paixão, Tatiane A. Sossai, Brunno G. Caza, Melissa Kronstad, James W. Peres, Nalu T. A. Santos, Daniel A. |
author_sort | Freitas, Gustavo J. C. |
collection | PubMed |
description | The phenotypic plasticity of Cryptococcus neoformans is widely studied and demonstrated in vitro, but its influence on pathogenicity remains unclear. In this study, we investigated the dynamics of cryptococcal cell and transcriptional remodeling during pulmonary infection in a murine model. We showed that in Cryptococcus neoformans, cell size reduction (cell body ≤ 3 µm) is important for initial adaptation during infection. This change was associated with reproductive fitness and tissue invasion. Subsequently, the fungus develops mechanisms aimed at resistance to the host’s immune response, which is determinant for virulence. We investigated the transcriptional changes involved in this cellular remodeling and found an upregulation of transcripts related to ribosome biogenesis at the beginning (6 h) of infection and a later (10 days) upregulation of transcripts involved in the inositol pathway, energy production, and the proteasome. Consistent with a role for the proteasome, we found that its inhibition delayed cell remodeling during infection with the H99 strain. Altogether, these results further our understanding of the infection biology of C. neoformans and provide perspectives to support therapeutic and diagnostic targets for cryptococcosis. |
format | Online Article Text |
id | pubmed-9740611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97406112022-12-11 The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection Freitas, Gustavo J. C. Gouveia-Eufrasio, Ludmila Emidio, Eluzia C. P. Carneiro, Hellem C. S. de Matos Baltazar, Ludmila Costa, Marliete C. Frases, Susana de Sousa Araújo, Glauber R. Paixão, Tatiane A. Sossai, Brunno G. Caza, Melissa Kronstad, James W. Peres, Nalu T. A. Santos, Daniel A. Cells Article The phenotypic plasticity of Cryptococcus neoformans is widely studied and demonstrated in vitro, but its influence on pathogenicity remains unclear. In this study, we investigated the dynamics of cryptococcal cell and transcriptional remodeling during pulmonary infection in a murine model. We showed that in Cryptococcus neoformans, cell size reduction (cell body ≤ 3 µm) is important for initial adaptation during infection. This change was associated with reproductive fitness and tissue invasion. Subsequently, the fungus develops mechanisms aimed at resistance to the host’s immune response, which is determinant for virulence. We investigated the transcriptional changes involved in this cellular remodeling and found an upregulation of transcripts related to ribosome biogenesis at the beginning (6 h) of infection and a later (10 days) upregulation of transcripts involved in the inositol pathway, energy production, and the proteasome. Consistent with a role for the proteasome, we found that its inhibition delayed cell remodeling during infection with the H99 strain. Altogether, these results further our understanding of the infection biology of C. neoformans and provide perspectives to support therapeutic and diagnostic targets for cryptococcosis. MDPI 2022-12-02 /pmc/articles/PMC9740611/ /pubmed/36497155 http://dx.doi.org/10.3390/cells11233896 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Freitas, Gustavo J. C. Gouveia-Eufrasio, Ludmila Emidio, Eluzia C. P. Carneiro, Hellem C. S. de Matos Baltazar, Ludmila Costa, Marliete C. Frases, Susana de Sousa Araújo, Glauber R. Paixão, Tatiane A. Sossai, Brunno G. Caza, Melissa Kronstad, James W. Peres, Nalu T. A. Santos, Daniel A. The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection |
title | The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection |
title_full | The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection |
title_fullStr | The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection |
title_full_unstemmed | The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection |
title_short | The Dynamics of Cryptococcus neoformans Cell and Transcriptional Remodeling during Infection |
title_sort | dynamics of cryptococcus neoformans cell and transcriptional remodeling during infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740611/ https://www.ncbi.nlm.nih.gov/pubmed/36497155 http://dx.doi.org/10.3390/cells11233896 |
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