Reciprocal modulation of ammonia and melanin production has implications for cryptococcal virulence.
Rosanna P BakerArturo CasadevallPublished in: Nature communications (2023)
The fungus Cryptococcus neoformans is the causative agent of cryptococcosis, a disease that is uniformly lethal unless treated with antifungal drugs, yet current regimens are hindered by host toxicity and pathogen resistance. An attractive alternative approach to combat this deadly disease is the direct targeting of pathogen-derived virulence mechanisms. C. neoformans expresses multiple virulence factors that have been studied previously as isolated entities. Among these, are urease, which increases phagosomal pH and promotes brain invasion, and melanization, which protects against immune cells and antifungal treatments. Here we report a reciprocal interdependency between these two virulence factors. Cells hydrolyzing urea release ammonia gas which acts at a distance to raise pH and increase melanization rates for nearby cells, which in turn reduces secretion of urease-carrying extracellular vesicles. This reciprocal relationship manifests as an emergent property that may explain why targeting isolated virulence mechanisms for drug development has been difficult and argues for a more holistic approach that considers the virulence composite.
Keyphrases
- escherichia coli
- pseudomonas aeruginosa
- biofilm formation
- staphylococcus aureus
- antimicrobial resistance
- candida albicans
- induced apoptosis
- cell cycle arrest
- room temperature
- oxidative stress
- cell death
- white matter
- cell proliferation
- living cells
- resting state
- fluorescent probe
- cell migration
- brain injury
- carbon dioxide
- subarachnoid hemorrhage