Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cells

The first step of any immune response is the recognition of foreign molecular structures inside the host organism. An important molecule that is generally foreign to eukaryotic cells is long double-stranded RNA (dsRNA), which can be generated during virus replication. The mechanisms of sensing viral...

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Main Authors: Brian C. Prince, Kalvin Chan, Claudia Rückert
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-08-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcimb.2023.1251204/full
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author Brian C. Prince
Kalvin Chan
Claudia Rückert
author_facet Brian C. Prince
Kalvin Chan
Claudia Rückert
author_sort Brian C. Prince
collection DOAJ
description The first step of any immune response is the recognition of foreign molecular structures inside the host organism. An important molecule that is generally foreign to eukaryotic cells is long double-stranded RNA (dsRNA), which can be generated during virus replication. The mechanisms of sensing viral dsRNA are well-studied in mammalian systems but are only poorly understood in insects, including disease vectors such as Culex quinquefasciatus mosquitoes. These mosquitoes are vectors for important arboviruses, such as West Nile virus, and Culex species mosquitoes are distributed across the globe in many temperate and tropical regions. The major antiviral response triggered by dsRNA in mosquitoes is RNA interference – a sequence-specific response which targets complementary viral RNA for degradation. However, here, we aimed to identify whether sequence-independent dsRNA sensing, mimicked by poly(I:C), can elicit an antiviral response. We observed a significant reduction in replication of La Crosse virus (LACV) in Cx. quinquefasciatus mosquito cells following poly(I:C) priming. We identified a number of antimicrobial peptides and Toll receptors that were upregulated at the transcript level by poly(I:C) stimulation. Notably, Toll6 was upregulated and we determined that a knockdown of Toll6 expression resulted also in increased LACV replication. Future efforts require genetic tools to validate whether the observed Toll6 antiviral activity is indeed linked to dsRNA sensing. However, large-scale functional genomic and proteomic approaches are also required to determine which downstream responses are part of the poly(I:C) elicited antiviral response.
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spelling doaj.art-afa6a764cad6475b88b42eebdc4be6172023-08-31T06:47:38ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882023-08-011310.3389/fcimb.2023.12512041251204Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cellsBrian C. PrinceKalvin ChanClaudia RückertThe first step of any immune response is the recognition of foreign molecular structures inside the host organism. An important molecule that is generally foreign to eukaryotic cells is long double-stranded RNA (dsRNA), which can be generated during virus replication. The mechanisms of sensing viral dsRNA are well-studied in mammalian systems but are only poorly understood in insects, including disease vectors such as Culex quinquefasciatus mosquitoes. These mosquitoes are vectors for important arboviruses, such as West Nile virus, and Culex species mosquitoes are distributed across the globe in many temperate and tropical regions. The major antiviral response triggered by dsRNA in mosquitoes is RNA interference – a sequence-specific response which targets complementary viral RNA for degradation. However, here, we aimed to identify whether sequence-independent dsRNA sensing, mimicked by poly(I:C), can elicit an antiviral response. We observed a significant reduction in replication of La Crosse virus (LACV) in Cx. quinquefasciatus mosquito cells following poly(I:C) priming. We identified a number of antimicrobial peptides and Toll receptors that were upregulated at the transcript level by poly(I:C) stimulation. Notably, Toll6 was upregulated and we determined that a knockdown of Toll6 expression resulted also in increased LACV replication. Future efforts require genetic tools to validate whether the observed Toll6 antiviral activity is indeed linked to dsRNA sensing. However, large-scale functional genomic and proteomic approaches are also required to determine which downstream responses are part of the poly(I:C) elicited antiviral response.https://www.frontiersin.org/articles/10.3389/fcimb.2023.1251204/fullmosquitoCuleximmune sensingdsRNA sensingTollarbovirus
spellingShingle Brian C. Prince
Kalvin Chan
Claudia Rückert
Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cells
Frontiers in Cellular and Infection Microbiology
mosquito
Culex
immune sensing
dsRNA sensing
Toll
arbovirus
title Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cells
title_full Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cells
title_fullStr Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cells
title_full_unstemmed Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cells
title_short Elucidating the role of dsRNA sensing and Toll6 in antiviral responses of Culex quinquefasciatus cells
title_sort elucidating the role of dsrna sensing and toll6 in antiviral responses of culex quinquefasciatus cells
topic mosquito
Culex
immune sensing
dsRNA sensing
Toll
arbovirus
url https://www.frontiersin.org/articles/10.3389/fcimb.2023.1251204/full
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