The virulence factor urease and its unexplored role in the metabolism of Cryptococcus neoformans

Author:

Toplis Barbra1ORCID,Bosch Caylin1,Schwartz Ilan S2,Kenyon Chris34ORCID,Boekhout Teun56,Perfect John R7,Botha Alfred1ORCID

Affiliation:

1. Department of Microbiology, Stellenbosch University, Matieland 7602, Stellenbosch, South Africa

2. Division of Infectious Diseases, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada, T6G 2G3

3. Sexually Transmitted Infection Unit, Institute of Tropical Medicine, 2000 Antwerp, Belgium

4. Department of Medicine, University of Cape Town, Cape Town 7925, South Africa

5. Westerdijk Fungal Biodiversity Institute, 3584CT Utrecht, The Netherlands

6. Institute for Biodiversity and Ecosystem Dynamics (IBED), University of Amsterdam, 1090 GE Amsterdam, The Netherlands

7. Division of Infectious Diseases, Duke University Medical Center, Durham, NC 27710-1000, North Carolina, USA

Abstract

ABSTRACT Cryptococcal urease is believed to be important for the degradation of exogenous urea that the yeast encounters both in its natural environment and within the human host. Endogenous urea produced by the yeast's own metabolic reactions, however, may also serve as a substrate for the urease enzyme. Using wild-type, urease-deletion mutant and urease-reconstituted strains of Cryptococcus neoformans H99, we studied reactions located up- and downstream from endogenous urea. We demonstrated that urease is important for cryptococcal growth and that, compared to nutrient-rich conditions at 26°C, urease activity is higher under nutrient-limited conditions at 37°C. Compared to cells with a functional urease enzyme, urease-deficient cells had significantly higher intracellular urea levels and also showed more arginase activity, which may act as a potential source of endogenous urea. Metabolic reactions linked to arginase were also affected, since urease-positive and urease-negative cells differed with respect to agmatinase activity, polyamine synthesis, and intracellular levels of proline and reactive oxygen species. Lastly, urease-deficient cells showed higher melanin levels at 26°C than wild-type cells, while the inverse was observed at 37°C. These results suggest that cryptococcal urease is associated with the functioning of key metabolic pathways within the yeast cell.

Funder

National Research Foundation

U.S. Public Health Service

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,General Medicine,Microbiology

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