Blocking Polyphosphate Mobilization Inhibits Pho4 Activation and Virulence in the Pathogen Candida albicans

被引:3
作者
Ahmed, Yasmin [1 ]
Ikeh, Melanie A. C. [1 ,3 ]
MacCallum, Donna M. [2 ]
Day, Alison M. [1 ]
Waldron, Kevin [1 ]
Quinn, Janet [1 ]
机构
[1] Newcastle Univ, Biosci Inst, Fac Med Sci, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Aberdeen, Inst Med Sci, Aberdeen Fungal Grp, Aberdeen, Scotland
[3] Univ Calif Merced, Sch Nat Sci, Dept Mol & Cell Biol, Merced, CA 95343 USA
来源
MBIO | 2022年 / 13卷 / 03期
基金
英国生物技术与生命科学研究理事会;
关键词
Candida albicans; morphogenesis; phosphate metabolism; stress response; virulence; EUKARYOTIC PHOSPHATE HOMEOSTASIS; SACCHAROMYCES-CEREVISIAE; CELL-CYCLE; TRANSCRIPTIONAL RESPONSE; GENE; METABOLISM; BINDING; STORAGE; STRESS; GROWTH;
D O I
10.1128/mbio.00342-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The ability of pathogenic fungi to obtain essential nutrients from the host is vital for virulence. In Candida albicans, acquisition of the macronutrient phosphate is regulated by the Pho4 transcription factor and is important for both virulence and resistance to host-encountered stresses. All cells store phosphate in the form of polyphosphate (polyP), a ubiquitous polymer comprising tens to hundreds of phosphate residues. Release of phosphate from polyP is one of the first responses evoked in response to phosphate starvation, and here, we sought to explore the importance of polyP mobilization in the pathobiology of C. albicans. We found that two polyphosphatases, Ppn1 and Ppx1, function redundantly to release phosphate from polyP in C. albicans. Strikingly, we reveal that blocking polyP mobilization prevents the activation of the Pho4 transcription factor: following P-i starvation, Pho4 fails to accumulate in the nucleus and induce P-i acquisition genes in ppn1 Delta ppx1 Delta cells. Consequently, ppn1 Delta ppx1 Delta cells display impaired resistance to the same range of stresses that require Pho4 for survival. In addition, cells lacking both polyphosphatases are exquisitely sensitive to DNA replication stress, indicating that polyP mobilization is needed to support the phosphate-demanding process of DNA replication. Blocking polyP mobilization also results in significant morphological defects, as ppn1 Delta ppx1 Delta cells form large pseudohypha-like cells that are resistant to serum-induced hypha formation. Thus, polyP mobilization impacts key processes important for the pathobiology of C. albicans, and consistent with this, we found that blocking this process attenuates the virulence of this important human fungal pathogen. IMPORTANCE Acquisition of the essential macronutrient phosphate is important for the virulence of Candida albicans, a major human fungal pathogen. All cells store phosphate as polyphosphate (polyP), which is rapidly mobilized when phosphate is limiting. Here, we identified the major phosphatases involved in releasing phosphate from polyP in C. albicans. By blocking this process, we found that polyP mobilization impacts many process that contribute to C. albicans pathogenesis. Notably, we found that blocking polyP mobilization inhibits activation of the Pho4 transcription factor, the master regulator of phosphate acquisition. In addition, cell cycle progression, stress resistance, morphogenetic switching, and virulence are all impaired in cells that cannot mobilize polyP. This study therefore provides new insight into the importance of polyP mobilization in promoting the virulence of C. albicans. As phosphate homeostasis strategies differ between fungal pathogen and host, this offers promise for the future development of antifungals. Acquisition of the essential macronutrient phosphate is important for the virulence of Candida albicans, a major human fungal pathogen. All cells store phosphate as polyphosphate (polyP), which is rapidly mobilized when phosphate is limiting.
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页数:20
相关论文
共 59 条
[1]   Polyphosphatase PPN1 of Saccharomyces cerevisiae: Switching of Exopolyphosphatase and Endopolyphosphatase Activities [J].
Andreeva, Nadezhda ;
Trilisenko, Ludmila ;
Eldarov, Mikhail ;
Kulakovskaya, Tatiana .
PLOS ONE, 2015, 10 (03)
[2]   Phosphate Homeostasis - A Vital Metabolic Equilibrium Maintained Through the INPHORS Signaling Pathway [J].
Austin, Sisley ;
Mayer, Andreas .
FRONTIERS IN MICROBIOLOGY, 2020, 11
[3]   Development of a yeast model to study the contribution of vacuolar polyphosphate metabolism to lysine polyphosphorylation [J].
Azevedo, Cristina ;
Desfougeres, Yann ;
Jiramongkol, Yannasittha ;
Partington, Hamish ;
Trakansuebkul, Sasanan ;
Singh, Jyoti ;
Steck, Nicole ;
Jessen, Henning J. ;
Saiardi, Adolfo .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2020, 295 (06) :1439-1451
[4]   Eukaryotic Phosphate Homeostasis: The Inositol Pyrophosphate Perspective [J].
Azevedo, Cristina ;
Saiardi, Adolfo .
TRENDS IN BIOCHEMICAL SCIENCES, 2017, 42 (03) :219-231
[5]   Protein Polyphosphorylation of Lysine Residues by Inorganic Polyphosphate [J].
Azevedo, Cristina ;
Livermore, Thomas ;
Saiardi, Adolfo .
MOLECULAR CELL, 2015, 58 (01) :71-82
[6]   Cell cycle arrest during S or M phase generates polarized growth via distinct signals in Candida albicans [J].
Bachewich, C ;
Nantel, A ;
Whiteway, M .
MOLECULAR MICROBIOLOGY, 2005, 57 (04) :942-959
[7]   Asynchronous cell cycle and asymmetric vacuolar inheritance in true hyphae of Candida albicans [J].
Barelle, CJ ;
Bohula, EA ;
Kron, SJ ;
Wessels, D ;
Soll, DR ;
Schäfer, A ;
Brown, AJP ;
Gow, NAR .
EUKARYOTIC CELL, 2003, 2 (03) :398-410
[8]   The vtc4 gene influences polyphosphate storage, morphogenesis, and virulence in the maize pathogen Ustilago maydis [J].
Boyce, Kylie J. ;
Kretschmer, Matthias ;
Kronstad, James W. .
EUKARYOTIC CELL, 2006, 5 (08) :1399-1409
[9]   Hidden Killers: Human Fungal Infections [J].
Brown, Gordon D. ;
Denning, David W. ;
Gow, Neil A. R. ;
Levitz, Stuart M. ;
Netea, Mihai G. ;
White, Theodore C. .
SCIENCE TRANSLATIONAL MEDICINE, 2012, 4 (165)
[10]   Polyphosphate is involved in cell cycle progression and genomic stability in Saccharomyces cerevisiae [J].
Bru, Samuel ;
Marc Martinez-Lainez, Joan ;
Hernandez-Ortega, Sara ;
Quandt, Eva ;
Torres-Torronteras, Javier ;
Marti, Ramon ;
Canadell, David ;
Arino, Joaquin ;
Sharma, Sushma ;
Jimenez, Javier ;
Clotet, Josep .
MOLECULAR MICROBIOLOGY, 2016, 101 (03) :367-380