Traversing the Cell Wall: The Chitinolytic Activity of Histoplasma capsulatum Extracellular Vesicles Facilitates Their Release
Authors:
- Alessandro F. ValdezAVAlessandro F. Valdez
- Taiane Nascimento de SouzaTSTaiane Nascimento de Souza
- Jhon Jhamilton Artunduaga BonillaJBJhon Jhamilton Artunduaga Bonilla
- Daniel Zamith-MirandaDZDaniel Zamith-Miranda
- Alicia Corbellini PifferAPAlicia Corbellini Piffer
- Glauber R. S. AraujoGAGlauber R. S. Araujo
- Allan J. GuimarãesAGAllan J. Guimarães
- Susana FrasesSFSusana Frases
- Alana Kelyene PereiraAPAlana Kelyene Pereira
- Taicia Pacheco FillTFTaicia Pacheco Fill
- Igor L. EstevaoIEIgor L. Estevao
- Angel TorresATAngel Torres
Open Access
- 27 October 2023
- journal article
- research article
- Published by MDPI AG in Journal of Fungi
- Vol. 9 (11) , 1052
Abstract
Histoplasma capsulatum is the causative agent of histoplasmosis. Treating this fungal infection conventionally has significant limitations, prompting the search for alternative therapies. In this context, fungal extracellular vesicles (EVs) hold relevant potential as both therapeutic agents and targets for the treatment of fungal infections. To explore this further, we conducted a study using pharmacological inhibitors of chitinase (methylxanthines) to investigate their potential to reduce EV release and its subsequent impact on fungal virulence in an in vivo invertebrate model. Our findings revealed that a subinhibitory concentration of the methylxanthine, caffeine, effectively reduces EV release, leading to a modulation of H. capsulatum virulence. To the best of our knowledge, this is the first reported instance of a pharmacological inhibitor that reduces fungal EV release without any observed fungicidal effects.Keywords
Funding Information
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) (E26/204.281/2021, 5U54MD007592)
- National Institutes of Health (NIH) (E26/204.281/2021, 5U54MD007592)
- Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (E26/204.281/2021, 5U54MD007592)
- Department of Defense (DoD) (E26/204.281/2021, 5U54MD007592)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (E26/204.281/2021, 5U54MD007592)
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (E26/204.281/2021, 5U54MD007592)
- UTEP Excellence Graduate School Fellowship (E26/204.281/2021, 5U54MD007592)
- the National Institute on Minority Health and Health Disparities (NIMHD) (E26/204.281/2021, 5U54MD007592)
This publication has 56 references indexed in Scilit:
- Vesicular mechanisms of traffic of fungal molecules to the extracellular spaceCurrent Opinion in Microbiology, 2013
- Cryptococcus neoformans-Derived Microvesicles Enhance the Pathogenesis of Fungal Brain InfectionPLOS ONE, 2012
- Vesicular transport inHistoplasma capsulatum: an effective mechanism for trans-cell wall transfer of proteins and lipids in ascomycetesCellular Microbiology, 2008
- Extracellular Vesicles Produced by Cryptococcus neoformans Contain Protein Components Associated with VirulenceEukaryotic Cell, 2008
- Vesicular Polysaccharide Export in Cryptococcus neoformans Is a Eukaryotic Solution to the Problem of Fungal Trans-Cell Wall TransportEukaryotic Cell, 2007
- Methylxanthine Drugs Are Chitinase Inhibitors: Investigation of Inhibition and Binding ModesChemistry & Biology, 2005
- Acidic Mammalian Chitinase in Asthmatic Th2 Inflammation and IL-13 Pathway ActivationScience, 2004
- RNA interference in Histoplasma capsulatum demonstrates a role for α‐(1,3)‐glucan in virulenceMolecular Microbiology, 2004
- Relationships of the Area under the Curve/MIC Ratio to Different Integral Endpoints of the Antimicrobial Effect: Gemifloxacin Pharmacodynamics in an In Vitro Dynamic ModelAntimicrobial Agents and Chemotherapy, 2001
- Modulation of Immune Responses in Murine Pulmonary HistoplasmosisThe Journal of Infectious Diseases, 1997