| Literature DB >> 27538790 |
Patrícia Alves de Castro1, Thaila Fernanda Dos Reis1, Stephen K Dolan2, Adriana Oliveira Manfiolli1, Neil Andrew Brown3, Gary W Jones2, Sean Doyle2, Diego M Riaño-Pachón4, Fábio Márcio Squina4, Camila Caldana4,5, Ashutosh Singh6, Maurizio Del Poeta6, Daisuke Hagiwara7, Rafael Silva-Rocha8, Gustavo H Goldman1.
Abstract
The serine-threonine kinase TOR, the Target of Rapamycin, is an important regulator of nutrient, energy and stress signaling in eukaryotes. Sch9, a Ser/Thr kinase of AGC family (the cAMP-dependent PKA, cGMP- dependent protein kinase G and phospholipid-dependent protein kinase C family), is a substrate of TOR. Here, we characterized the fungal opportunistic pathogen Aspergillus fumigatus Sch9 homologue (SchA). The schA null mutant was sensitive to rapamycin, high concentrations of calcium, hyperosmotic stress and SchA was involved in iron metabolism. The ΔschA null mutant showed increased phosphorylation of SakA, the A. fumigatus Hog1 homologue. The schA null mutant has increased and decreased trehalose and glycerol accumulation, respectively, suggesting SchA performs different roles for glycerol and trehalose accumulation during osmotic stress. The schA was transcriptionally regulated by osmotic stress and this response was dependent on SakA and MpkC. The double ΔschA ΔsakA and ΔschA ΔmpkC mutants were more sensitive to osmotic stress than the corresponding parental strains. Transcriptomics and proteomics identified direct and indirect targets of SchA post-exposure to hyperosmotic stress. Finally, ΔschA was avirulent in a low dose murine infection model. Our results suggest there is a complex network of interactions amongst the A. fumigatus TOR, SakA and SchA pathways.Entities:
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Year: 2016 PMID: 27538790 PMCID: PMC5207228 DOI: 10.1111/mmi.13484
Source DB: PubMed Journal: Mol Microbiol ISSN: 0950-382X Impact factor: 3.501