Mitochondrial proline catabolism activates Ras1/cAMP/PKA-induced filamentation in Candida albicans

Autor: Kicki Ryman, Klas I. Udekwu, Björn Brindefalk, Meliza Ward, Axel Wallstrom, Per O. Ljungdahl, Fitz Gerald S. Silao
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Arginine
Yeast and Fungal Models
Mitochondrion
Pathology and Laboratory Medicine
Biochemistry
chemistry.chemical_compound
White Blood Cells
Mice
Adenosine Triphosphate
Animal Cells
Gene expression
Candida albicans
Medicine and Health Sciences
Morphogenesis
Cyclic AMP
Amino Acids
Energy-Producing Organelles
Candida
2. Zero hunger
chemistry.chemical_classification
Fungal Pathogens
0303 health sciences
biology
Virulence
Chemistry
Organic Compounds
Monosaccharides
Eukaryota
Catabolism
Ornithine
Cell biology
Amino acid
Mitochondria
Amino acid permease
Experimental Organism Systems
Medical Microbiology
Physical Sciences
Pathogens
Basic Amino Acids
Cellular Structures and Organelles
Cellular Types
Research Article
Signal Transduction
Proline
lcsh:QH426-470
Immune Cells
Immunology
Carbohydrates
Hyphae
Mycology
Bioenergetics
Research and Analysis Methods
Microbiology
Fungal Proteins
03 medical and health sciences
Proline Oxidase
Animals
Humans
Microbial Pathogens
030304 developmental biology
Blood Cells
030306 microbiology
Macrophages
Organic Chemistry
Chemical Compounds
Organisms
Fungi
Biology and Life Sciences
Proteins
Cyclic Amino Acids
Cell Biology
biology.organism_classification
Cyclic AMP-Dependent Protein Kinases
Yeast
lcsh:Genetics
Glucose
Metabolism
RAW 264.7 Cells
Animal Studies
ras Proteins
Developmental Biology
Zdroj: PLoS Genetics, Vol 15, Iss 2, p e1007976 (2019)
PLoS Genetics
DOI: 10.1101/374777
Popis: Amino acids are among the earliest identified inducers of yeast-to-hyphal transitions in Candida albicans, an opportunistic fungal pathogen of humans. Here, we show that the morphogenic amino acids arginine, ornithine and proline are internalized and metabolized in mitochondria via a PUT1- and PUT2-dependent pathway that results in enhanced ATP production. Elevated ATP levels correlate with Ras1/cAMP/PKA pathway activation and Efg1-induced gene expression. The magnitude of amino acid-induced filamentation is linked to glucose availability; high levels of glucose repress mitochondrial function thereby dampening filamentation. Furthermore, arginine-induced morphogenesis occurs more rapidly and independently of Dur1,2-catalyzed urea degradation, indicating that mitochondrial-generated ATP, not CO2, is the primary morphogenic signal derived from arginine metabolism. The important role of the SPS-sensor of extracellular amino acids in morphogenesis is the consequence of induced amino acid permease gene expression, i.e., SPS-sensor activation enhances the capacity of cells to take up morphogenic amino acids, a requisite for their catabolism. C. albicans cells engulfed by murine macrophages filament, resulting in macrophage lysis. Phagocytosed put1-/- and put2-/- cells do not filament and exhibit reduced viability, consistent with a critical role of mitochondrial proline metabolism in virulence.
Author summary Candida albicans is an opportunistic fungal pathogen that exists as a benign member of the human microbiome. Immunosuppression, or microbial dysbiosis, can predispose an individual to infection, enabling this fungus to evade innate immune cells and initiate a spectrum of pathologies, including superficial mucocutaneous or even life-threatening invasive infections. Infectious growth is attributed to an array of virulence characteristics, a major one being the ability to switch morphologies from round yeast-like to elongated hyphal cells. Here we report that mitochondrial proline catabolism is required to induce hyphal growth of C. albicans cells in phagosomes of engulfing macrophages, which is key to evade killing by macrophages. The finding that proline catabolism, also required for the utilization of arginine and ornithine, is required to sustain the energy demands of hyphal growth underscores the central role of mitochondria in fungal virulence. In contrast to existing dogma, we show that in C. albicans, mitochondrial function is subject to glucose repression, amino acid-induced signals are strictly dependent on Ras1 and the SPS-sensor is the primary sensor of extracellular amino acids. The results provide a clear example of how C. albicans cells sense and respond to host nutrients to ensure proper nutrient uptake and survival.
Databáze: OpenAIRE