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Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model

The small molecule (molecular mass <900 Daltons) composition of extracellular vesicles (EVs) produced by the pathogenic fungus Cryptococcus gattii is unknown, which limits the understanding of the functions of cryptococcal EVs. In this study, we analyzed the composition of small molecules in samp...

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Autores principales: Reis, Flavia C. G., Costa, Jonas H., Honorato, Leandro, Nimrichter, Leonardo, Fill, Taícia P., Rodrigues, Marcio L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008140/
https://www.ncbi.nlm.nih.gov/pubmed/33796117
http://dx.doi.org/10.3389/fimmu.2021.654574
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author Reis, Flavia C. G.
Costa, Jonas H.
Honorato, Leandro
Nimrichter, Leonardo
Fill, Taícia P.
Rodrigues, Marcio L.
author_facet Reis, Flavia C. G.
Costa, Jonas H.
Honorato, Leandro
Nimrichter, Leonardo
Fill, Taícia P.
Rodrigues, Marcio L.
author_sort Reis, Flavia C. G.
collection PubMed
description The small molecule (molecular mass <900 Daltons) composition of extracellular vesicles (EVs) produced by the pathogenic fungus Cryptococcus gattii is unknown, which limits the understanding of the functions of cryptococcal EVs. In this study, we analyzed the composition of small molecules in samples obtained from solid cultures of C. gattii by a combination of chromatographic and spectrometric approaches, and untargeted metabolomics. This analysis revealed previously unknown components of EVs, including small peptides with known biological functions in other models. The peptides found in C. gattii EVs had their chemical structure validated by chemical approaches and comparison with authentic standards, and their functions tested in a Galleria mellonella model of cryptococcal infection. One of the vesicular peptides (isoleucine-proline-isoleucine, Ile-Pro-Ile) improved the survival of G. mellonella lethally infected with C. gattii or C. neoformans. These results indicate that small molecules exported in EVs are biologically active in Cryptococcus. Our study is the first to characterize a fungal EV molecule inducing protection, pointing to an immunological potential of extracellular peptides produced by C. gattii.
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spelling pubmed-80081402021-03-31 Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model Reis, Flavia C. G. Costa, Jonas H. Honorato, Leandro Nimrichter, Leonardo Fill, Taícia P. Rodrigues, Marcio L. Front Immunol Immunology The small molecule (molecular mass <900 Daltons) composition of extracellular vesicles (EVs) produced by the pathogenic fungus Cryptococcus gattii is unknown, which limits the understanding of the functions of cryptococcal EVs. In this study, we analyzed the composition of small molecules in samples obtained from solid cultures of C. gattii by a combination of chromatographic and spectrometric approaches, and untargeted metabolomics. This analysis revealed previously unknown components of EVs, including small peptides with known biological functions in other models. The peptides found in C. gattii EVs had their chemical structure validated by chemical approaches and comparison with authentic standards, and their functions tested in a Galleria mellonella model of cryptococcal infection. One of the vesicular peptides (isoleucine-proline-isoleucine, Ile-Pro-Ile) improved the survival of G. mellonella lethally infected with C. gattii or C. neoformans. These results indicate that small molecules exported in EVs are biologically active in Cryptococcus. Our study is the first to characterize a fungal EV molecule inducing protection, pointing to an immunological potential of extracellular peptides produced by C. gattii. Frontiers Media S.A. 2021-03-16 /pmc/articles/PMC8008140/ /pubmed/33796117 http://dx.doi.org/10.3389/fimmu.2021.654574 Text en Copyright © 2021 Reis, Costa, Honorato, Nimrichter, Fill and Rodrigues. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Reis, Flavia C. G.
Costa, Jonas H.
Honorato, Leandro
Nimrichter, Leonardo
Fill, Taícia P.
Rodrigues, Marcio L.
Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model
title Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model
title_full Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model
title_fullStr Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model
title_full_unstemmed Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model
title_short Small Molecule Analysis of Extracellular Vesicles Produced by Cryptococcus gattii: Identification of a Tripeptide Controlling Cryptococcal Infection in an Invertebrate Host Model
title_sort small molecule analysis of extracellular vesicles produced by cryptococcus gattii: identification of a tripeptide controlling cryptococcal infection in an invertebrate host model
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008140/
https://www.ncbi.nlm.nih.gov/pubmed/33796117
http://dx.doi.org/10.3389/fimmu.2021.654574
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