Secretome profiling of Cryptococcus neoformans reveals regulation of a subset of virulence-associated proteins and potential biomarkers by protein kinase A

• Published in: BMC microbiology Vol. 15; no. 1; p. 206
• Main Authors: Geddes, Jennifer M H, Croll, Daniel, Caza, Mélissa, Stoynov, Nikolay, Foster, Leonard J, Kronstad, James W
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 09.10.2015; BioMed Central
• Subjects: Analysis; Animals; Biological markers; Biomarkers; Biomarkers - analysis; Cellular signal transduction; Chemical Precipitation; Chromatography, Liquid; Cryptococcus neoformans - chemistry; Culture Media - chemistry; Cyclic AMP - metabolism; Cyclic AMP-Dependent Protein Kinases - metabolism; Enzymes; Female; Fungal Proteins - secretion; Genes; Glucose; Influence; Kinases; Macrophages; Macrophages - microbiology; Metabolism; Mice, Inbred BALB C; Proteins; Proteome - analysis; Proteomics; Signal transduction; Tandem Mass Spectrometry; Virulence; Virulence (Microbiology); Virulence Factors - metabolism
• DOI: 10.1186/s12866-015-0532-3
• ISSN: 1471-2180

The pathogenic yeast Cryptococcus neoformans causes life-threatening meningoencephalitis in individuals suffering from HIV/AIDS. The cyclic-AMP/protein kinase A (PKA) signal transduction pathway regulates the production of extracellular virulence factors in C. neoformans, but the influence of the pathway on the secretome has not been investigated. In this study, we performed quantitative proteomics using galactose-inducible and glucose-repressible expression of the PKA1 gene encoding the catalytic subunit of PKA to identify regulated proteins in the secretome. The proteins in the supernatants of cultures of C. neoformans were precipitated and identified using liquid chromatography-coupled tandem mass spectrometry. We also employed multiple reaction monitoring in a targeted approach to identify fungal proteins in samples from macrophages after phagocytosis of C. neoformans cells, as well as from the blood and bronchoalveolar fluid of infected mice. We identified 61 secreted proteins and found that changes in PKA1 expression influenced the extracellular abundance of five proteins, including the Cig1 and Aph1 proteins with known roles in virulence. We also observed a change in the secretome profile upon induction of Pka1 from proteins primarily involved in catabolic and metabolic processes to an expanded set that included proteins for translational regulation and the response to stress. We further characterized the secretome data using enrichment analysis and by predicting conventional versus non-conventional secretion. Targeted proteomics of the Pka1-regulated proteins allowed us to identify the secreted proteins in lysates of phagocytic cells containing C. neoformans, and in samples from infected mice. This analysis also revealed that modulation of PKA1 expression influences the intracellular survival of cryptococcal cells upon phagocytosis. Overall, we found that the cAMP/PKA pathway regulates specific components of the secretome including proteins that affect the virulence of C. neoformans. The detection of secreted cryptococcal proteins from infected phagocytic cells and tissue samples suggests their potential utility as biomarkers of infection. The proteomics data are available via ProteomeXchange with identifiers PXD002731 and PASS00736.