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Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors
The World Health Organization estimates that more than half of the world’s population is at risk for vector-borne diseases, including arboviruses. Because many arboviruses are mosquito borne, investigation of the insect immune response will help identify targets to reduce the spread of arboviruses....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6871768/ https://www.ncbi.nlm.nih.gov/pubmed/31722209 http://dx.doi.org/10.1016/j.celrep.2019.10.029 |
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author | Ahlers, Laura R.H. Trammell, Chasity E. Carrell, Grace F. Mackinnon, Sophie Torrevillas, Brandi K. Chow, Clement Y. Luckhart, Shirley Goodman, Alan G. |
author_facet | Ahlers, Laura R.H. Trammell, Chasity E. Carrell, Grace F. Mackinnon, Sophie Torrevillas, Brandi K. Chow, Clement Y. Luckhart, Shirley Goodman, Alan G. |
author_sort | Ahlers, Laura R.H. |
collection | PubMed |
description | The World Health Organization estimates that more than half of the world’s population is at risk for vector-borne diseases, including arboviruses. Because many arboviruses are mosquito borne, investigation of the insect immune response will help identify targets to reduce the spread of arboviruses. Here, we use a genetic screening approach to identify an insulin-like receptor as a component of the immune response to arboviral infection. We determine that vertebrate insulin reduces West Nile virus (WNV) replication in Drosophila melanogaster as well as WNV, Zika, and dengue virus titers in mosquito cells. Mechanistically, we show that insulin signaling activates the JAK/STAT, but not RNAi, pathway via ERK to control infection in Drosophila cells and Culex mosquitoes through an integrated immune response. Finally, we validate that insulin priming of adult female Culex mosquitoes through a blood meal reduces WNV infection, demonstrating an essential role for insulin signaling in insect antiviral responses to human pathogens. |
format | Online Article Text |
id | pubmed-6871768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68717682019-11-21 Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors Ahlers, Laura R.H. Trammell, Chasity E. Carrell, Grace F. Mackinnon, Sophie Torrevillas, Brandi K. Chow, Clement Y. Luckhart, Shirley Goodman, Alan G. Cell Rep Article The World Health Organization estimates that more than half of the world’s population is at risk for vector-borne diseases, including arboviruses. Because many arboviruses are mosquito borne, investigation of the insect immune response will help identify targets to reduce the spread of arboviruses. Here, we use a genetic screening approach to identify an insulin-like receptor as a component of the immune response to arboviral infection. We determine that vertebrate insulin reduces West Nile virus (WNV) replication in Drosophila melanogaster as well as WNV, Zika, and dengue virus titers in mosquito cells. Mechanistically, we show that insulin signaling activates the JAK/STAT, but not RNAi, pathway via ERK to control infection in Drosophila cells and Culex mosquitoes through an integrated immune response. Finally, we validate that insulin priming of adult female Culex mosquitoes through a blood meal reduces WNV infection, demonstrating an essential role for insulin signaling in insect antiviral responses to human pathogens. 2019-11-12 /pmc/articles/PMC6871768/ /pubmed/31722209 http://dx.doi.org/10.1016/j.celrep.2019.10.029 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Ahlers, Laura R.H. Trammell, Chasity E. Carrell, Grace F. Mackinnon, Sophie Torrevillas, Brandi K. Chow, Clement Y. Luckhart, Shirley Goodman, Alan G. Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors |
title | Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors |
title_full | Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors |
title_fullStr | Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors |
title_full_unstemmed | Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors |
title_short | Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors |
title_sort | insulin potentiates jak/stat signaling to broadly inhibit flavivirus replication in insect vectors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6871768/ https://www.ncbi.nlm.nih.gov/pubmed/31722209 http://dx.doi.org/10.1016/j.celrep.2019.10.029 |
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