Abstract

Cryptococcus neoformans survives host temperature and regulates cell wall integrity via a calcium-dependent phosphatase, calcineurin. However, downstream effectors of C. neoformans calcineurin are largely unknown. In S. cerevisiae and other fungal species, a calcineurin-dependent transcription factor Crz1, translocates to nuclei upon activation and triggers expression of target genes. We now show that the C. neoformans Crz1 ortholog (Crz1/Sp1), previously identified as a protein kinase C target during starvation, is a bona fide target of calcineurin under non-starvation conditions, during cell wall stress and growth at high temperature. Both the calcineurin-defective mutant, Δcna1, and a CRZ1/SP1 mutant (Δcrz1) were susceptible to cell wall perturbing agents. Furthermore, expression of the chitin synthase encoding gene, CHS6, was reduced in both mutants. We tracked the subcellular localization of Crz1-GFP in WT C. neoformans and Δcna1 in response to different stimuli, in the presence and absence of the calcineurin inhibitor, FK506. Exposure to elevated temperature (30–37°C vs 25°C) and extracellular calcium caused calcineurin-dependent nuclear accumulation of Crz1-GFP. Unexpectedly, 1M salt and heat shock triggered calcineurin-independent Crz1-GFP sequestration within cytosolic and nuclear puncta. To our knowledge, punctate cytosolic distribution, as opposed to nuclear targeting, is a unique feature of C. neoformans Crz1. We conclude that Crz1 is selectively activated by calcium/calcineurin-dependent and independent signals depending on the environmental conditions.

Highlights

  • Cryptococcus neoformans var. grubii causes life-threatening meningoencephalitis especially in immunosuppressed individuals, including recipients of organ transplants

  • We identified a short glutamine-rich region in C. neoformans Crz1 (CnCrz1) which is found in S. cerevisiae Crz1

  • In this study we have demonstrated that CnCrz1 is activated by calcineurin in response to physiological temperature, extracellular calcium and cell wall perturbation, as manifested by its nuclear localization under these conditions

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Summary

Introduction

Cryptococcus neoformans var. grubii causes life-threatening meningoencephalitis especially in immunosuppressed individuals, including recipients of organ transplants. Grubii causes life-threatening meningoencephalitis especially in immunosuppressed individuals, including recipients of organ transplants. In this group, mortality approaches 40% in those with central nervous system infection [1,2]. Cyclosporine (CsA) and tacrolimus (FK506) inhibit calcineurin by binding cyclophilin A and FKBP12, respectively. These compounds target the mammalian and the fungal homologues of calcineurin and possess both, antirejection and antifungal activities. Targeting of calcineurin in C. neoformans with immunosuppressive inhibitors, or their nonimmunosuppressive derivatives, combined with other antifungals, opens a new and promising avenue for drug development [4]. A synergistic effect of FK506 combined with bafilomycin A1, fluconazole, or caspofungin acetate has already been demonstrated in vitro [5]

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