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Loquacious modulates flaviviral RNA replication in mosquito cells

Arthropod-borne viruses infect both mosquito and mammalian hosts. While much is known about virus-host interactions that modulate viral gene expression in their mammalian host, much less is known about the interactions that involve inhibition, subversion or avoidance strategies in the mosquito host....

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Autores principales: Shivaprasad, Shwetha, Weng, Kuo-Feng, Ooi, Yaw Shin, Belk, Julia, Carette, Jan E., Flynn, Ryan, Sarnow, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089905/
https://www.ncbi.nlm.nih.gov/pubmed/35482886
http://dx.doi.org/10.1371/journal.ppat.1010163
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author Shivaprasad, Shwetha
Weng, Kuo-Feng
Ooi, Yaw Shin
Belk, Julia
Carette, Jan E.
Flynn, Ryan
Sarnow, Peter
author_facet Shivaprasad, Shwetha
Weng, Kuo-Feng
Ooi, Yaw Shin
Belk, Julia
Carette, Jan E.
Flynn, Ryan
Sarnow, Peter
author_sort Shivaprasad, Shwetha
collection PubMed
description Arthropod-borne viruses infect both mosquito and mammalian hosts. While much is known about virus-host interactions that modulate viral gene expression in their mammalian host, much less is known about the interactions that involve inhibition, subversion or avoidance strategies in the mosquito host. A novel RNA-Protein interaction detection assay was used to detect proteins that directly or indirectly bind to dengue viral genomes in infected mosquito cells. Membrane-associated mosquito proteins Sec61A1 and Loquacious (Loqs) were found to be in complex with the viral RNA. Depletion analysis demonstrated that both Sec61A1 and Loqs have pro-viral functions in the dengue viral infectious cycle. Co-localization and pull-down assays showed that Loqs interacts with viral protein NS3 and both full-length and subgenomic viral RNAs. While Loqs coats the entire positive-stranded viral RNA, it binds selectively to the 3’ end of the negative-strand of the viral genome. In-depth analyses showed that the absence of Loqs did not affect translation or turnover of the viral RNA but modulated viral replication. Loqs also displayed pro-viral functions for several flaviviruses in infected mosquito cells, suggesting a conserved role for Loqs in flavivirus-infected mosquito cells.
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spelling pubmed-90899052022-05-11 Loquacious modulates flaviviral RNA replication in mosquito cells Shivaprasad, Shwetha Weng, Kuo-Feng Ooi, Yaw Shin Belk, Julia Carette, Jan E. Flynn, Ryan Sarnow, Peter PLoS Pathog Research Article Arthropod-borne viruses infect both mosquito and mammalian hosts. While much is known about virus-host interactions that modulate viral gene expression in their mammalian host, much less is known about the interactions that involve inhibition, subversion or avoidance strategies in the mosquito host. A novel RNA-Protein interaction detection assay was used to detect proteins that directly or indirectly bind to dengue viral genomes in infected mosquito cells. Membrane-associated mosquito proteins Sec61A1 and Loquacious (Loqs) were found to be in complex with the viral RNA. Depletion analysis demonstrated that both Sec61A1 and Loqs have pro-viral functions in the dengue viral infectious cycle. Co-localization and pull-down assays showed that Loqs interacts with viral protein NS3 and both full-length and subgenomic viral RNAs. While Loqs coats the entire positive-stranded viral RNA, it binds selectively to the 3’ end of the negative-strand of the viral genome. In-depth analyses showed that the absence of Loqs did not affect translation or turnover of the viral RNA but modulated viral replication. Loqs also displayed pro-viral functions for several flaviviruses in infected mosquito cells, suggesting a conserved role for Loqs in flavivirus-infected mosquito cells. Public Library of Science 2022-04-28 /pmc/articles/PMC9089905/ /pubmed/35482886 http://dx.doi.org/10.1371/journal.ppat.1010163 Text en © 2022 Shivaprasad et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shivaprasad, Shwetha
Weng, Kuo-Feng
Ooi, Yaw Shin
Belk, Julia
Carette, Jan E.
Flynn, Ryan
Sarnow, Peter
Loquacious modulates flaviviral RNA replication in mosquito cells
title Loquacious modulates flaviviral RNA replication in mosquito cells
title_full Loquacious modulates flaviviral RNA replication in mosquito cells
title_fullStr Loquacious modulates flaviviral RNA replication in mosquito cells
title_full_unstemmed Loquacious modulates flaviviral RNA replication in mosquito cells
title_short Loquacious modulates flaviviral RNA replication in mosquito cells
title_sort loquacious modulates flaviviral rna replication in mosquito cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089905/
https://www.ncbi.nlm.nih.gov/pubmed/35482886
http://dx.doi.org/10.1371/journal.ppat.1010163
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