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Loquacious modulates flaviviral RNA replication in mosquito cells

  • Shwetha Shivaprasad*
  • , Kuo Feng Weng
  • , Yaw Shin Ooi
  • , Julia Belk
  • , Jan E. Carette
  • , Ryan Flynn
  • , Peter Sarnow*
  • *此作品的通信作者
  • Stanford University
  • Stanford ChEM-H

研究成果: 期刊稿件文章同行評審

9 引文 斯高帕斯(Scopus)

摘要

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.

原文英語
文章編號e1010163
期刊PLoS Pathogens
18
發行號4
DOIs
出版狀態已出版 - 04 2022

文獻附註

Publisher Copyright:
Copyright: © 2022 Shivaprasad et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

UN SDG

此研究成果有助於以下永續發展目標

  1. SDG3 健康與福祉
    SDG3 健康與福祉

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