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A Role for the Insulin Receptor in the Suppression of Dengue Virus and Zika Virus in Wolbachia-Infected Mosquito Cells

Authors :
Prasad N. Paradkar
Gerard Terradas
Gholamreza Haqshenas
Jean-Bernard Duchemin
Christian Doerig
Elizabeth A. McGraw
Monash University [Clayton]
Australian Animal Health Laboratory (AAHL)
CSIRO Health and Biosecurity [Australia]
Commonwealth Scientific and Industrial Research Organisation [Canberra] (CSIRO)-Commonwealth Scientific and Industrial Research Organisation [Canberra] (CSIRO)
Pennsylvania State University (Penn State)
Penn State System
The research was supported by the C.D. group and NHMRC project grant APP1103804 (to E.M.).
Source :
Cell Reports, Cell Reports, Elsevier Inc, 2019, 26 (3), pp.529-535.e3. ⟨10.1016/j.celrep.2018.12.068⟩
Publication Year :
2019
Publisher :
HAL CCSD, 2019.

Abstract

International audience; Wolbachia-infected mosquitoes are refractory to super-infection with arthropod-borne pathogens, but the role of host cell signaling proteins in pathogen-blocking mechanisms remains to be elucidated. Here, we use an antibody microarray approach to provide a comprehensive picture of the signaling response of Aedes aegypti-derived cells to Wolbachia. This approach identifies the host cell insulin receptor as being downregulated by the bacterium. Furthermore, siRNA-mediated knockdown and treatment with a small-molecule inhibitor of the insulin receptor kinase concur to assign a crucial role for this enzyme in the replication of dengue and Zika viruses in cultured mosquito cells. Finally, we show that the production of Zika virus in Wolbachia-free live mosquitoes is impaired by treatment with the selective inhibitor mimicking Wolbachia infection. This study identifies Wolbachia-mediated downregulation of insulin receptor kinase activity as a mechanism contributing to the blocking of super-infection by arboviruses.

Details

Language :
English
ISSN :
22111247
Database :
OpenAIRE
Journal :
Cell Reports, Cell Reports, Elsevier Inc, 2019, 26 (3), pp.529-535.e3. ⟨10.1016/j.celrep.2018.12.068⟩
Accession number :
edsair.doi.dedup.....f8dee77c03908a4c5f436cf1ef9409a5