RT Journal Article SR Electronic(1) A1 Acosta-Zaldivar, Maikel A1 Qi, Wanjun A1 Liu, Ning-Ning A1 Diray-Arce, Joann A1 Walker, Louise A. A1 Kottom, Theodore J. A1 Kelly, Rachel A1 Yuan, Min A1 Asara, John M. A1 Lasky-Su, Jessica Ann A1 Levy, Ofer A1 Limper, Andrew H. A1 Gow, Neil A. R. A1 Köhler, Julia RuthYR 2021 T1 Candida albicans phosphate transport, facilitating nucleotide sugar biosynthesis, contributes to cell wall stability. JF Access Microbiology, VO 3 IS 12 OP SP po0036 DO https://doi.org/10.1099/acmi.cc2021.po0036 PB Microbiology Society, SN 2516-8290, AB The Candida albicans high-affinity phosphate transporter Pho84 is required for normal Target of Rapamycin signaling, oxidative stress resistance and virulence of this fungal pathogen. It also contributes to C. albicans’ tolerance of two antifungal drug classes, polyenes and echinocandins. Echinocandins inhibit biosynthesis of a major cell wall component, beta-1,3-glucan. Cells lacking Pho84 were hypersensitive to other forms of cell wall stress beyond echinocandin exposure, while their cell wall integrity signaling response was weak. Metabolomics experiments showed that levels of phosphoric intermediates, including nucleotides like ATP and nucleotide sugars, were low in pho84 mutant compared to wild type cells recovering from phosphate starvation. Non-phosphoric precursors like nucleobases and nucleosides were elevated. Outer cell wall phosphomannan biosynthesis requires a nucleotide sugar,GDP-mannose. The nucleotide sugar UDP-glucose is the substrate of enzymes that synthesize two major structural cell wall polysaccharides, beta-1,3- and beta-1,6-glucan. Another nucleotide sugar, UDP-N-acetylglucosamine, is the substrate of chitin synthases which produce a stabilizing component of the intercellular septum and of lateral cell walls. Lack of Pho84 activity, and phosphate starvation, potentiated pharmacological or genetic perturbation of these enzymes. Our model is that low substrate concentrations of beta-D-glucan- and chitin synthases diminish enzymatic reaction rates and potentiate pharmacologic inhibitors to decrease the yield of their cell wall-stabilizing products. Phosphate import is not conserved between fungal and human cells, and humans do not synthesize beta-D-glucans or chitin. Hence inhibiting these processes simultaneously could yield potent antifungal effects with low toxicity to humans., UL https://www.microbiologyresearch.org/content/journal/acmi/10.1099/acmi.cc2021.po0036