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bioRxiv · 10.1101/374777

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

Silao, F. G. S.·Ward, M.·Ryman, K.·Wallstrom, A.·Brindefalk, B.·Udekwu, K.·Ljungdahl, P. O.
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Abstract

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 do not lyse macrophages, consistent with a critical role of mitochondrial proline metabolism in virulence.

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Silao, F. G. S., Ward, M., Ryman, K., Wallstrom, A., Brindefalk, B., Udekwu, K., Ljungdahl, P. O.. 2018-07-23. Mitochondrial proline catabolism activates Ras1/cAMP/PKA-induced filamentation in Candida albicans. https://doi.org/10.1101/374777

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