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      Characterization of Extracellular Vesicles Produced by Aspergillus fumigatus Protoplasts

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          Abstract

          Fungal cells use extracellular vesicles (EVs) to export biologically active molecules to the extracellular space. In this study, we used protoplasts of Aspergillus fumigatus, a major fungal pathogen, as a model to evaluate the role of EV production in cell wall biogenesis. Our results demonstrated that wall-less A. fumigatus exports plasma membrane-derived EVs containing a complex combination of proteins and glycans. Our report is the first to characterize fungal EVs in the absence of a cell wall. Our results suggest that protoplasts represent a promising model for functional studies of fungal vesicles.

          ABSTRACT

          Extracellular vesicles (EVs) are membranous compartments produced by yeast and mycelial forms of several fungal species. One of the difficulties in perceiving the role of EVs during the fungal life, and particularly in cell wall biogenesis, is caused by the presence of a thick cell wall. One alternative to have better access to these vesicles is to use protoplasts. This approach has been investigated here with Aspergillus fumigatus, one of the most common opportunistic fungal pathogens worldwide. Analysis of regenerating protoplasts by scanning electron microscopy and fluorescence microscopy indicated the occurrence of outer membrane projections in association with surface components and the release of particles with properties resembling those of fungal EVs. EVs in culture supernatants were characterized by transmission electron microscopy and nanoparticle tracking analysis. Proteomic and glycome analysis of EVs revealed the presence of a complex array of enzymes related to lipid/sugar metabolism, pathogenic processes, and cell wall biosynthesis. Our data indicate that (i) EV production is a common feature of different morphological stages of this major fungal pathogen and (ii) protoplastic EVs are promising tools for undertaking studies of vesicle functions in fungal cells.

          IMPORTANCE Fungal cells use extracellular vesicles (EVs) to export biologically active molecules to the extracellular space. In this study, we used protoplasts of Aspergillus fumigatus, a major fungal pathogen, as a model to evaluate the role of EV production in cell wall biogenesis. Our results demonstrated that wall-less A. fumigatus exports plasma membrane-derived EVs containing a complex combination of proteins and glycans. Our report is the first to characterize fungal EVs in the absence of a cell wall. Our results suggest that protoplasts represent a promising model for functional studies of fungal vesicles.

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          Aspergillus fumigatus and Aspergillosis in 2019

          Aspergillus fumigatus is a saprotrophic fungus; its primary habitat is the soil. In its ecological niche, the fungus has learned how to adapt and proliferate in hostile environments. This capacity has helped the fungus to resist and survive against human host defenses and, further, to be responsible for one of the most devastating lung infections in terms of morbidity and mortality. In this review, we will provide (i) a description of the biological cycle of A. fumigatus ; (ii) a historical perspective of the spectrum of aspergillus disease and the current epidemiological status of these infections; (iii) an analysis of the modes of immune response against Aspergillus in immunocompetent and immunocompromised patients; (iv) an understanding of the pathways responsible for fungal virulence and their host molecular targets, with a specific focus on the cell wall; (v) the current status of the diagnosis of different clinical syndromes; and (vi) an overview of the available antifungal armamentarium and the therapeutic strategies in the clinical context. In addition, the emergence of new concepts, such as nutritional immunity and the integration and rewiring of multiple fungal metabolic activities occurring during lung invasion, has helped us to redefine the opportunistic pathogenesis of A. fumigatus .
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            Vesicular polysaccharide export in Cryptococcus neoformans is a eukaryotic solution to the problem of fungal trans-cell wall transport.

            The mechanisms by which macromolecules are transported through the cell wall of fungi are not known. A central question in the biology of Cryptococcus neoformans, the causative agent of cryptococcosis, is the mechanism by which capsular polysaccharide synthesized inside the cell is exported to the extracellular environment for capsule assembly and release. We demonstrate that C. neoformans produces extracellular vesicles during in vitro growth and animal infection. Vesicular compartments, which are transferred to the extracellular space by cell wall passage, contain glucuronoxylomannan (GXM), a component of the cryptococcal capsule, and key lipids, such as glucosylceramide and sterols. A correlation between GXM-containing vesicles and capsule expression was observed. The results imply a novel mechanism for the release of the major virulence factor of C. neoformans whereby polysaccharide packaged in lipid vesicles crosses the cell wall and the capsule network to reach the extracellular environment.
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              The induction and repression of nitrate reductase in the fungus Aspergillus nidulans.

              D. Cove (1966)
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                Author and article information

                Contributors
                Role: Editor
                Journal
                mSphere
                mSphere
                msph
                msph
                mSphere
                mSphere
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2379-5042
                12 August 2020
                Jul-Aug 2020
                : 5
                : 4
                : e00476-20
                Affiliations
                [a ]Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
                [b ]Department of Mycology, Institut Pasteur, Paris, France
                [c ]Plateforme Protéomique, Unité de Spectrométrie de Masse pour la Biologie (MSBio), Centre de Ressources et Recherches Technologiques (C2RT), USR 2000 CNRS, Institut Pasteur, Paris, France
                [d ]Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
                [e ]Centro Nacional de Biologia Estrutural e Bioimagem, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
                [f ]School of Life Sciences, Arizona State University, Tempe, Arizona, USA
                [g ]Plateforme de Microscopie Ultrastructurale, Imagepole, Institut Pasteur, Paris, France
                [h ]School of Medicine, University of Crete, Heraklion, Crete, Greece
                [i ]Instituto Carlos Chagas, Fundação Oswaldo Cruz, Curitiba, Brazil
                University of Georgia
                Author notes
                Address correspondence to Anne Beauvais, anne.beauvais@ 123456pasteur.fr , or Marcio L. Rodrigues, marcio.rodrigues@ 123456fiocruz.br .

                Anne Beauvais and Marcio L. Rodrigues share co-senior authorship of this article.

                Citation Rizzo J, Chaze T, Miranda K, Roberson RW, Gorgette O, Nimrichter L, Matondo M, Latgé J-P, Beauvais A, Rodrigues ML. 2020. Characterization of extracellular vesicles produced by Aspergillus fumigatus protoplasts. mSphere 5:e00476-20. https://doi.org/10.1128/mSphere.00476-20.

                Author information
                https://orcid.org/0000-0001-5538-6471
                https://orcid.org/0000-0002-6081-3439
                Article
                mSphere00476-20
                10.1128/mSphere.00476-20
                7426166
                32817450
                e417ead6-7e12-42fc-9615-a79ad31b499b
                Copyright © 2020 Rizzo et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 20 May 2020
                : 22 July 2020
                Page count
                supplementary-material: 2, Figures: 6, Tables: 1, Equations: 0, References: 77, Pages: 16, Words: 10637
                Funding
                Funded by: MCTI | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), https://doi.org/10.13039/501100003593;
                Award ID: 301304/2017-3
                Award Recipient :
                Funded by: Agence Nationale de la Recherche (ANR), https://doi.org/10.13039/501100001665;
                Award ID: ANR-10-LABX-62-IBEID
                Award Recipient :
                Funded by: Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), https://doi.org/10.13039/501100002322;
                Award ID: 88887.142840/2017-00
                Award ID: Finance code 001
                Award Recipient :
                Funded by: Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ), https://doi.org/10.13039/501100004586;
                Award ID: E-26/201.991/2015
                Award Recipient :
                Funded by: Fondation pour la Recherche Médicale (FRM), https://doi.org/10.13039/501100002915;
                Award ID: DEQ20150331722 LATGE Equipe FRM 2015
                Award Recipient :
                Funded by: Fundação Oswaldo Cruz (FIOCRUZ), https://doi.org/10.13039/501100006507;
                Award ID: VPPCB-007- FIO-18 and VPPIS-001-FIO18
                Award Recipient :
                Funded by: Ministério da Saúde (Ministry of Health), https://doi.org/10.13039/501100006506;
                Award ID: 405520/2018-2
                Award Recipient :
                Categories
                Research Article
                Molecular Biology and Physiology
                Custom metadata
                July/August 2020

                aspergillus fumigatus,conidia,protoplasts,extracellular vesicles,aspergillus

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