Hexokinase and Glucokinases Are Essential for Fitness and Virulence in the Pathogenic Yeast Candida albicans

• Published in: Frontiers in microbiology Vol. 10; p. 327
• Main Authors: Laurian, Romain, Dementhon, Karine, Doumèche, Bastien, Soulard, Alexandre, Noel, Thierry, Lemaire, Marc, Cotton, Pascale
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media 2019; Frontiers Media S.A
• Subjects: Biochemistry, Molecular Biology; Candida albicans; glucokinase; glucose repression; glycolysis; hexokinase; hyphal transition; Life Sciences; Microbiology; Microbiology and Parasitology; Mycology; Candida albicans; hyphal transition; virulence; glycolysis; glucokinase; glucose repression; hexokinase
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2019.00327

The pathogenic yeast is both a powerful commensal and a pathogen of humans that can infect wide range of organs and body sites. Metabolic flexibility promotes infection and commensal colonization by this opportunistic pathogen. Yeast cell survival depends upon assimilation of fermentable and non-fermentable locally available carbon sources. Physiologically relevant sugars like glucose and fructose are present at low levels in host niches. However, because glucose is the preferred substrate for energy and biosynthesis of structural components, its efficient detection and metabolism are fundamental for the metabolic adaptation of the pathogen. We explored and characterized the hexose kinase system composed of one hexokinase ( Hxk2) and two glucokinases ( Glk1 and Glk4). Using a set of mutant strains, we found that hexose phosphorylation is mostly performed by Hxk2, which sustains growth on hexoses. Our data on hexokinase and glucokinase expression point out an absence of cross regulation mechanisms at the transcription level and different regulatory pathways. In the presence of glucose, Hxk2 migrates in the nucleus and contributes to the glucose repression signaling pathway. In addition, Hxk2 participates in oxidative, osmotic and cell wall stress responses, while glucokinases are overexpressed under hypoxia. Hexose phosphorylation is a key step necessary for filamentation that is affected in the hexokinase mutant. Virulence of this mutant is clearly impacted in the and macrophage models. Filamentation, glucose phosphorylation and stress response defects of the hexokinase mutant prevent host killing by . By contributing to metabolic flexibility, stress response and morphogenesis, hexose kinase enzymes play an essential role in the virulence of .