Corrected and republished from: "Extracellular Vesicle Formation in Cryptococcus deuterogattii Impacts Fungal Virulence".
Rafael F CastelliAlana PereiraLeandro HonoratoAlessandro ValdezHaroldo C de OliveiraJaqueline M BazioliAne W A GarciaTabata D'Maiella Freitas KlimeckFlavia C G ReisAmanda C Camillo-AndradeMarlon D M SantosPaulo C CarvalhoÓscar ZaragozaCharley C StaatsLeonardo NimrichterTaícia P FillMarcio Lourenço RodriguesPublished in: Infection and immunity (2024)
Small molecules are components of fungal extracellular vesicles (EVs), but their biological roles are only superficially known. NOP16 is a eukaryotic gene that is required for the activity of benzimidazoles against Cryptococcus deuterogattii . In this study, during the phenotypic characterization of C. deuterogattii mutants expected to lack NOP16 expression, we observed a reduced EV production. Whole-genome sequencing, RNA-Seq, and cellular proteomics revealed that, contrary to our initial findings, these mutants expressed Nop16 but exhibited altered expression of 14 genes potentially involved in sugar transport. Based on this observation, we designated these mutant strains as Past1 and Past2, representing p otentially a ltered s ugar t ransport. Analysis of the small molecule composition of EVs produced by wild-type cells and the Past1 and Past2 mutant strains revealed not only a reduced number of EVs but also an altered small molecule composition. In a Galleria mellonella model of infection, the Past1 and Past2 mutant strains were hypovirulent. The hypovirulent phenotype was reverted when EVs produced by wild-type cells, but not mutant EVs, were co-injected with the mutant cells in G. mellonella . These results connect EV biogenesis, cargo, and cryptococcal virulence.
Keyphrases
- wild type
- small molecule
- escherichia coli
- induced apoptosis
- rna seq
- single cell
- cell cycle arrest
- poor prognosis
- pseudomonas aeruginosa
- genome wide
- staphylococcus aureus
- endoplasmic reticulum stress
- antimicrobial resistance
- biofilm formation
- mass spectrometry
- cell death
- dna methylation
- cystic fibrosis
- pi k akt
- copy number