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Phenotypic characterization of HAM1 , a novel mating regulator of the fungal pathogen Cryptococcus neoformans .

Authors :
Yee EA
Ross RL
Santiago-Tirado FH
Source :
BioRxiv : the preprint server for biology [bioRxiv] 2024 Mar 31. Date of Electronic Publication: 2024 Mar 31.
Publication Year :
2024

Abstract

Cryptococcus neoformans is a fungal pathogen responsible for >200,000 yearly cases with a mortality as high as 81%. This burden results, in part, from an incomplete understanding of its pathogenesis and ineffective antifungal treatments; hence, there is a pressing need to understand the biology and host interactions of this yeast to develop improved treatments. Protein palmitoylation is important for cryptococcal virulence, and we previously identified the substrates of its main palmitoyl transferase. One of them was encoded by the uncharacterized gene CNAG_02129. In the filamentous fungus Neurospora crassa , a homolog of this gene named HAM-13 plays a role in proper cellular communication and filament fusion. In Cryptococcus , cellular communication is essential during mating, therefore we hypothesized that CNAG_02129, which we named HAM1 , may play a role in mating. We found that ham1 Δ mutants produce more fusion products during mating, filament more robustly, and exhibit competitive fitness defects under mating and non-mating conditions. Additionally, we found several differences with the major virulence factor, the polysaccharide capsule, that may affect virulence, consistent with prior studies linking virulence to mating. We observed that ham1 Δ mutants have decreased capsule attachment and transfer but exhibit higher amounts of exopolysaccharide shedding and biofilm production. Lastly, HAM1 expression is significantly lower in mating media relative to non-mating conditions, consistent with it acting as a negative regulator of mating. Understanding the connection between mating and virulence in C. neoformans may open new avenues of investigation into ways to improve the treatment of this disease.

Details

Language :
English
ISSN :
2692-8205
Database :
MEDLINE
Journal :
BioRxiv : the preprint server for biology
Accession number :
38585947
Full Text :
https://doi.org/10.1101/2023.09.18.558251