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Extracellular Vesicles from Virulent Induce TLR4 and Dectin-1 Expression in Innate Cells and Promote Enhanced Th1/Th17 Response

Overview
Journal Virulence
Specialty Microbiology
Date 2024 Mar 21
PMID 38511558
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Abstract

Extracellular vesicles (EVs) are membrane-enclosed nanoparticles that transport several biomolecules and are involved in important mechanisms and functions related to the pathophysiology of fungal diseases. EVs from , the main causative agent of Paracoccidioidomycosis (PCM), modulate the immune response of macrophages. In this study, we assessed the EVs proteome from a virulent isolated from granulomatous lesions and compared their immunomodulatory ability with EVs isolated from the fungus before the animal passage (control EVs) when challenging macrophages and dendritic cells (DCs). Proteome showed that virulent EVs have a higher abundance of virulence factors such as GP43, protein 14-3-3, GAPDH, as well as virulence factors never described in PCM, such as aspartyl aminopeptidase and a SidJ analogue compared with control EVs. Virulent extracellular vesicles induced higher expression of TLR4 and Dectin-1 than control EVs in macrophages and dendritic cells (DCs). In opposition, a lower TLR2 expression was induced by virulent EVs. Additionally, virulent EVs induced lower expression of CD80, CD86 and TNF-α, but promoted a higher expression of IL-6 and IL-10, suggesting that EVs isolated from virulent -yeast promote a milder DCs and macrophage maturation. Herein, we showed that EVs from virulent fungi stimulated a higher frequency of Th1/Tc1, Th17, and Treg cells, which gives new insights into fungal extracellular vesicles. Taken together, our results suggest that utilizes its EVs as virulence bags that manipulate the immune system in its favour, creating a milder immune response and helping with fungal evasion from the immune system.

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References
1.
Grundlinger M, Gsaller F, Schrettl M, Lindner H, Haas H . Aspergillus fumigatus SidJ mediates intracellular siderophore hydrolysis. Appl Environ Microbiol. 2013; 79(23):7534-6. PMC: 3837724. DOI: 10.1128/AEM.01285-13. View

2.
Cavassani K, Campanelli A, Moreira A, Vancim J, Vitali L, Mamede R . Systemic and local characterization of regulatory T cells in a chronic fungal infection in humans. J Immunol. 2006; 177(9):5811-8. DOI: 10.4049/jimmunol.177.9.5811. View

3.
Ritchie M, Phipson B, Wu D, Hu Y, Law C, Shi W . limma powers differential expression analyses for RNA-sequencing and microarray studies. Nucleic Acids Res. 2015; 43(7):e47. PMC: 4402510. DOI: 10.1093/nar/gkv007. View

4.
Ashburner M, Ball C, Blake J, Botstein D, Butler H, Cherry J . Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet. 2000; 25(1):25-9. PMC: 3037419. DOI: 10.1038/75556. View

5.
Dalod M, Chelbi R, Malissen B, Lawrence T . Dendritic cell maturation: functional specialization through signaling specificity and transcriptional programming. EMBO J. 2014; 33(10):1104-16. PMC: 4193918. DOI: 10.1002/embj.201488027. View