Characterization and functional analysis of zinc trafficking in the human fungal pathogen Candida parapsilosis

Author:

Takács Tamás12,Németh Mihály Tibor12,Bohner Flóra12,Vágvölgyi Csaba2,Jankovics Ferenc34,Wilson Duncan5,Gácser Attila126

Affiliation:

1. HCEMM-USZ Fungal Pathogens Research Group, Department of Microbiology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary

2. Department of Microbiology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary

3. Department of Medical Biology, Szent-Györgyi Albert Medical School, University of Szeged, Szeged, Hungary

4. Institute of Genetics, Biological Research Centre, Szeged, Hungary

5. Medical Research Council Centre for Medical Mycology at the University of Exeter, Exeter, UK

6. MTA-SZTE ‘Lendület’ Mycobiome Research Group, University of Szeged, Szeged, Hungary

Abstract

The zinc restriction and zinc toxicity are part of host defence, called nutritional immunity. The crucial role of zinc homeostasis in microbial survival within a host is established, but little is known about these processes in the opportunistic human fungal pathogen Candida parapsilosis. Our in silico predictions suggested the presence of at least six potential zinc transporters (ZnTs) in C. parapsilosis —orthologues of ZRC1 , ZRT3 and ZRT101 —but an orthologue of PRA1 zincophore was not found. In addition, we detected a species-specific gene expansion of the novel ZnT ZRT2, as we identified three orthologue genes in the genome of C. parapsilosis . Based on predictions, we created homozygous mutant strains of the potential ZnTs and characterized them. Despite the apparent gene expansion of ZRT2 in C. parapsilosis , only CpZRT21 was essential for growth in a zinc-depleted acidic environment, in addition we found that CpZrc1 is essential for zinc detoxification and also protects the fungi against the elimination of murine macrophages. Significantly, we demonstrated that C. parapsilosis forms zincosomes in a Zrc1-independent manner and zinc detoxification is mediated by the vacuolar importer CpZrc1. Our study defines the functions of C. parapsilosis ZnTs, including a species-specific survival and zinc detoxification system.

Funder

Magyar Tudományos Akadémia

Magyarország Kormánya

University of Exeter

Wellcome Trust

Publisher

The Royal Society

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,General Neuroscience

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