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Publication : Global Reprogramming of Host Kinase Signaling in Response to Fungal Infection.

First Author  Pandey A Year  2017
Journal  Cell Host Microbe Volume  21
Issue  5 Pages  637-649.e6
PubMed ID  28494245 Mgi Jnum  J:360231
Mgi Id  MGI:7797551 Doi  10.1016/j.chom.2017.04.008
Citation  Pandey A, et al. (2017) Global Reprogramming of Host Kinase Signaling in Response to Fungal Infection. Cell Host Microbe 21(5):637-649.e6
abstractText  Cryptococcus neoformans (Cn) is a deadly fungal pathogen whose intracellular lifestyle is important for virulence. Host mechanisms controlling fungal phagocytosis and replication remain obscure. Here, we perform a global phosphoproteomic analysis of the host response to Cryptococcus infection. Our analysis reveals numerous and diverse host proteins that are differentially phosphorylated following fungal ingestion by macrophages, thereby indicating global reprogramming of host kinase signaling. Notably, phagocytosis of the pathogen activates the host autophagy initiation complex (AIC) and the upstream regulatory components LKB1 and AMPKalpha, which regulate autophagy induction through their kinase activities. Deletion of Prkaa1, the gene encoding AMPKalpha1, in monocytes results in resistance to fungal colonization of mice. Finally, the recruitment of AIC components to nascent Cryptococcus-containing vacuoles (CnCVs) regulates the intracellular trafficking and replication of the pathogen. These findings demonstrate that host AIC regulatory networks confer susceptibility to infection and establish a proteomic resource for elucidating host mechanisms that regulate fungal intracellular parasitism.
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