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Eukaryotic Cell, October 2006, p. 1788-1796, Vol. 5, No. 10
1535-9778/06/$08.00+0     doi:10.1128/EC.00158-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Cch1 Mediates Calcium Entry in Cryptococcus neoformans and Is Essential in Low-Calcium Environments{triangledown}

Min Liu,1 Ping Du,1 Garrett Heinrich,2 Gary M. Cox,2 and Angie Gelli1*

Department of Medical Pharmacology and Toxicology, University of California, Davis, Genome and Biomedical Sciences Facility, Davis, California 95616,1 Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 277102

Received 31 May 2006/ Accepted 21 August 2006

The ability of Cryptococcus neoformans to grow at the mammalian body temperature (37°C to 39°C) is a well-established virulence factor. Growth of C. neoformans at this physiological temperature requires calcineurin, a Ca2+/calmodulin-dependent protein phosphatase. When cytosolic calcium concentrations are low (~50 to 100 nM), calcineurin is inactive and becomes active only when cytosolic calcium concentrations rise (~1 to 10 µM) through the activation of calcium channels. In this study we analyzed the function of Cch1 in C. neoformans and found that Cch1 is a Ca2+-permeable channel that mediates calcium entry in C. neoformans. Analysis of the Cch1 protein sequence revealed differences in the voltage sensor (S4 regions), suggesting that Cch1 may have diminished voltage sensitivity or possibly an alternative gating mechanism. The inability of the cch1 mutant to grow under conditions of limited extracellular calcium concentrations ([Ca2+]extracellular, ~100 nM) suggested that Cch1 was required for calcium uptake in low-calcium environments. These results are consistent with the role of ScCch1 in mediating high-affinity calcium uptake in Saccharomyces cerevisiae. Although the growth defect of the cch1 mutant under conditions of limited [Ca2+]extracellular (~100 nM) became more severe with increasing temperature (25°C to 38.5°), this temperature sensitivity was not observed when the cch1 mutant was grown on rich medium ([Ca2+]extracellular, ~0.140 mM). Accordingly, the cch1 mutant strain displayed only attenuated virulence when tested in the mouse inhalation model of cryptococcosis, further suggesting that C. neoformans may have a limited requirement for Cch1 and that this requirement appears to include ion stress tolerance.

* Corresponding author. Mailing address: Department of Medical Pharmacology and Toxicology, University of California, Davis, Genome and Biomedical Sciences Facility, Davis, CA 95616. Phone: (530) 754-6179. Fax: (530) 752-7710. E-mail: acgelli{at}ucdavis.edu.

{triangledown} Published ahead of print on 1 September 2006.

Eukaryotic Cell, October 2006, p. 1788-1796, Vol. 5, No. 10
1535-9778/06/$08.00+0     doi:10.1128/EC.00158-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



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