Functional connections between cell cycle and proteostasis in the regulation of Candida albicans morphogenesis

Morphological plasticity is a key virulence trait for many fungal pathogens. For the opportunistic fungal pathogen Candida albicans, transitions among yeast, pseudohyphal, and hyphal forms are critical for virulence, because the morphotypes play distinct roles in the infection process. C. albicans morphogenesis is induced in response to many host-relevant conditions and is regulated by complex signaling pathways and cellular processes. Perturbation of either cell-cycle progression or protein homeostasis induces C. albicans filamentation, demonstrating that these processes play a key role in morphogenetic control. Regulators such as cyclin-dependent kinases, checkpoint proteins, the proteasome, the heat shock protein Hsp90, and the heat shock transcription factor Hsf1 all influence morphogenesis, often through interconnected effects on the cell cycle and proteostasis. This review highlights the major cell-cycle and proteostasis regulators that modulate morphogenesis and discusses how these two processes intersect to regulate this key virulence trait.

Automated summary

Morphological plasticity is a key virulence trait for many fungal pathogens, with Candida albicans transitioning among yeast, pseudohyphal, and hyphal forms being critical for its virulence. This morphogenesis is induced in response to host-relevant conditions and is regulated by complex signaling pathways and cellular processes, with regulators such as cyclin-dependent kinases, checkpoint proteins, proteasome, Hsp90, and Hsf1 influencing the process through interconnected effects on the cell cycle and proteostasis.