| Literature DB >> 30550790 |
Priya S Shah1, Nichole Link2, Gwendolyn M Jang3, Phillip P Sharp4, Tongtong Zhu5, Danielle L Swaney3, Jeffrey R Johnson3, John Von Dollen3, Holly R Ramage6, Laura Satkamp3, Billy Newton3, Ruth Hüttenhain3, Marine J Petit7, Tierney Baum8, Amanda Everitt8, Orly Laufman9, Michel Tassetto9, Michael Shales3, Erica Stevenson3, Gabriel N Iglesias10, Leila Shokat3, Shashank Tripathi11, Vinod Balasubramaniam12, Laurence G Webb5, Sebastian Aguirre11, A Jeremy Willsey13, Adolfo Garcia-Sastre14, Katherine S Pollard15, Sara Cherry6, Andrea V Gamarnik10, Ivan Marazzi16, Jack Taunton17, Ana Fernandez-Sesma18, Hugo J Bellen19, Raul Andino20, Nevan J Krogan21.
Abstract
Mosquito-borne flaviviruses, including dengue virus (DENV) and Zika virus (ZIKV), are a growing public health concern. Systems-level analysis of how flaviviruses hijack cellular processes through virus-host protein-protein interactions (PPIs) provides information about their replication and pathogenic mechanisms. We used affinity purification-mass spectrometry (AP-MS) to compare flavivirus-host interactions for two viruses (DENV and ZIKV) in two hosts (human and mosquito). Conserved virus-host PPIs revealed that the flavivirus NS5 protein suppresses interferon stimulated genes by inhibiting recruitment of the transcription complex PAF1C and that chemical modulation of SEC61 inhibits DENV and ZIKV replication in human and mosquito cells. Finally, we identified a ZIKV-specific interaction between NS4A and ANKLE2, a gene linked to hereditary microcephaly, and showed that ZIKV NS4A causes microcephaly in Drosophila in an ANKLE2-dependent manner. Thus, comparative flavivirus-host PPI mapping provides biological insights and, when coupled with in vivo models, can be used to unravel pathogenic mechanisms.Entities:
Keywords: ANKLE2; Drosophila; PAF1C; Sec61; Zika virus; dengue virus; endoplasmic reticulum; flavivirus; interferon stimulated genes; microcephaly; proteomics
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Year: 2018 PMID: 30550790 PMCID: PMC6474419 DOI: 10.1016/j.cell.2018.11.028
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582