Traversing the Cell Wall: The Chitinolytic Activity of Histoplasma capsulatum Extracellular Vesicles Facilitates Their Release

Author:

Valdez Alessandro F.123ORCID,de Souza Taiane Nascimento13,Bonilla Jhon Jhamilton Artunduaga1,Zamith-Miranda Daniel23,Piffer Alicia Corbellini14,Araujo Glauber R. S.5ORCID,Guimarães Allan J.67ORCID,Frases Susana57ORCID,Pereira Alana Kelyene8ORCID,Fill Taicia Pacheco8,Estevao Igor L.9ORCID,Torres Angel9ORCID,Almeida Igor C.9,Nosanchuk Joshua D.23ORCID,Nimrichter Leonardo17ORCID

Affiliation:

1. Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, RJ, Brazil

2. Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA

3. Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA

4. Unité Biologie des ARN des Pathogènes Fongiques, Départament de Mycologie, Institut Pasteur, Université Paris Cité, F-75015 Paris, France

5. Laboratório de Biofísica de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, RJ, Brazil

6. Instituto Biomédico, Departamento de Microbiologia e Parasitologia—MIP, Universidade Federal Fluminense, Niterói 24210-130, RJ, Brazil

7. Rede Micologia, RJ, FAPERJ, Rio de Janeiro 21941-902, RJ, Brazil

8. Instituto de Química, Universidade Estadual de Campinas, Campinas, São Paulo 13083-970, SP, Brazil

9. Department of Biological Sciences, Border Biomedical Research Center, University of Texas El Paso, El Paso, TX 79902, USA

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.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

National Institutes of Health

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Department of Defense

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado de São Paulo

UTEP Excellence Graduate School Fellowship

the National Institute on Minority Health and Health Disparities

Publisher

MDPI AG

Subject

Plant Science,Ecology, Evolution, Behavior and Systematics,Microbiology (medical)

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