Geddes Jennifer M H, Croll Daniel, Caza Mélissa, Stoynov Nikolay, Foster Leonard J, Kronstad James W
Michael Smith Laboratories, University of British Columbia, Vancouver, BC, V6T 1Z4, Canada.
Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, Canada.
BMC Microbiol. 2015 Oct 9;15:206. doi: 10.1186/s12866-015-0532-3.
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.
致病性酵母新型隐球菌可在感染人类免疫缺陷病毒/获得性免疫综合征(HIV/AIDS)的个体中引发危及生命的脑膜脑炎。环磷酸腺苷/蛋白激酶A(PKA)信号转导通路调控新型隐球菌细胞外毒力因子的产生,但该通路对分泌蛋白组的影响尚未得到研究。在本研究中,我们利用半乳糖诱导型和葡萄糖抑制型表达编码PKA催化亚基的PKA1基因进行定量蛋白质组学研究,以鉴定分泌蛋白组中受调控的蛋白质。
新型隐球菌培养上清液中的蛋白质经沉淀后,采用液相色谱-串联质谱进行鉴定。我们还采用多反应监测的靶向方法,鉴定新型隐球菌细胞被巨噬细胞吞噬后,以及感染小鼠血液和支气管肺泡灌洗液样本中的真菌蛋白。
我们鉴定出61种分泌蛋白,发现PKA1表达的变化影响了5种蛋白的细胞外丰度,包括在毒力方面具有已知作用的Cig1和Aph1蛋白。我们还观察到,诱导Pka1后,分泌蛋白组图谱发生了变化,从主要参与分解代谢和代谢过程的蛋白质,转变为包括参与翻译调控和应激反应的蛋白质的扩展集合。我们通过富集分析和预测常规分泌与非常规分泌,进一步对分泌蛋白组数据进行了表征。对Pka1调控蛋白的靶向蛋白质组学研究,使我们能够鉴定含有新型隐球菌的吞噬细胞裂解物以及感染小鼠样本中的分泌蛋白。该分析还表明,PKA1表达的调节影响吞噬作用后隐球菌细胞的细胞内存活。
总体而言,我们发现cAMP/PKA通路调节分泌蛋白组的特定成分,包括影响新型隐球菌毒力的蛋白质。从感染的吞噬细胞和组织样本中检测到分泌的隐球菌蛋白,表明它们作为感染生物标志物具有潜在用途。蛋白质组学数据可通过ProteomeXchange获取,标识符为PXD002731和PASS00736。