While many questions remain regarding the role of mammalian small RNA pathways in antiviral defense, it is clear that the presence of conserved antiviral silencing pathways in invertebrate organisms plays an important role in the transmission of mosquito-borne viral diseases. Although the small interfering RNA (siRNA) pathway appears to provide the primary antiviral immune response in invertebrate organisms, several lines of evidence suggest an antiviral role for a somatic piwi-interacting RNA (piRNA) pathway present in disease vector mosquitoes. First, the production of piRNAs from viral RNAs described in various mosquito cell lines and tissues is itself suggestive of an antiviral function. Second, in contrast to the enhanced disease phenotype associated with siRNA-deficient mutant flies infected with viral pathogens, an antiviral immune response directed by virus-derived piRNAs modulates the pathogenicity of alphavirus infections in siRNA-deficient mutant mosquito cell lines. Conversly, knocking down components of the piRNA pathway in mosquito cells has been shown to enhance alphavirus replication. Thus, our research plan is designed to test the hypothesis that a non-canonical piRNA pathway present in the soma of mosquito vectors is acting concurrently with the small interfering RNA (siRNA) pathway to form a coordinated, redundant antiviral defense. A model of hierarchical antiviral immunity in disease vectors, based on previous studies in our laboratory, provides a framework for experiments to define the biogenic pathway of viral piRNA production, dissect the relative contributions of the piRNA and siRNA pathways to antiviral immunity and genome integrity, and evaluate the potential of manipulating endogenous piRNA clusters as a broad-spectrum control strategy.

Public Health Relevance

The overall goal of this proposal is to understand the role of piwi-interacting RNAs (piRNAs) in mosquito antiviral immunity. In addition to increasing understanding of antiviral immune responses in disease vectors, the proposed research will assess the potential of piRNA-based control strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI119081-04
Application #
9284377
Study Section
Vector Biology Study Section (VB)
Program Officer
Costero-Saint Denis, Adriana
Project Start
2016-12-01
Project End
2020-04-30
Budget Start
2017-05-01
Budget End
2018-04-30
Support Year
4
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Texas A&M Agrilife Research
Department
Zoology
Type
Earth Sciences/Resources
DUNS #
847205713
City
College Station
State
TX
Country
United States
Zip Code
77843
Samuel, Glady Hazitha; Adelman, Zach N; Myles, Kevin M (2018) Antiviral Immunity and Virus-Mediated Antagonism in Disease Vector Mosquitoes. Trends Microbiol 26:447-461
Samuel, Glady Hazitha; Adelman, Zach N; Myles, Kevin M (2016) Temperature-dependent effects on the replication and transmission of arthropod-borne viruses in their insect hosts. Curr Opin Insect Sci 16:108-113
Samuel, Glady Hazitha; Wiley, Michael R; Badawi, Atif et al. (2016) Yellow fever virus capsid protein is a potent suppressor of RNA silencing that binds double-stranded RNA. Proc Natl Acad Sci U S A 113:13863-13868