Cryptococcus neoformans is an opportunistic fungal pathogen that causes cryptococcal
meningoencephalitis, particularly in immunocompromised patients. The fungal cell wall is an excellent target for antifungal therapies as it is an essential organelle that provides cell structure and integrity, it is needed for the localization or attachment of known
virulence factors, including the polysaccharide capsule,
melanin, and
phospholipase, and it is critical for host-pathogen interactions. In C. neoformans,
chitosan produced by the enzymatic removal of acetyl groups from nascent
chitin polymers has been implicated as an important component of the vegetative cell wall. In this study, we identify four putative
chitin/polysaccharide deacetylases in C. neoformans. We have demonstrated that three of these deacetylases, Cda1, Cda2, and Cda3, can account for all of the
chitosan produced during vegetative growth in culture, but the function for one, Fpd1, remains undetermined. The data suggest a model for
chitosan production in vegetatively growing C. neoformans where the three
chitin deacetylases convert
chitin generated by the
chitin synthase Chs3 into
chitosan. Utilizing a collection of
chitin/
polysaccharide deacetylase deletion strains, we determined that during vegetative growth,
chitosan helps to maintain cell integrity and
aids in bud separation. Additionally,
chitosan is necessary for maintaining normal capsule width and the lack of
chitosan results in a "leaky
melanin" phenotype. Our analysis indicates that
chitin deacetylases and the
chitosan made by them may prove to be excellent antifungal targets.