Proceedings of the National Academy of Sciences · 2009 · 610 citations · 46 references
Life SciencesInfectious DiseasesMolecular BiologySignal TransductionTranscriptional RegulationVirologyAntiviral ImmunityImmune Signaling PathwaysInnate Immune ResponseInsect Immune ResponsesMosquito BiologyVector-pathogen InteractionsAntiviral Signaling PathwaysJak-stat Signaling In ImmunityJak-stat Signaling PathwayMosquito Immune ResponseMosquito ImmunityResistance In MosquitoesViral Immune ResponsesViral Restriction Factors
Here, we show that the major mosquito vector for dengue virus uses the JAK-STAT pathway to control virus infection. Dengue virus infection in Aedes aegypti mosquitoes activates the JAK-STAT immune signaling pathway. The mosquito's susceptibility to dengue virus infection increases when the JAK-STAT pathway is suppressed through RNAi depletion of its receptor Domeless (Dome) and the Janus kinase (Hop), whereas mosquitoes become more resistant to the virus when the negative regulator of the JAK-STAT pathway, PIAS, is silenced. The JAK-STAT pathway exerts its anti-dengue activity presumably through one or several STAT-regulated effectors. We have identified, and partially characterized, two JAK-STAT pathway-regulated and infection-responsive dengue virus restriction factors (DVRFs) that contain putative STAT-binding sites in their promoter regions. Our data suggest that the JAK-STAT pathway is part of the A. aegypti mosquito's anti-dengue defense and may act independently of the Toll pathway and the RNAi-mediated antiviral defenses.
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Genome Sequence of <i>Aedes aegypti</i> , a Major Arbovirus Vector
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