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DnaJ homolog Hdj2 Facilitates Japanese Encephalitis Virus Replication

  • Robert Wang
  • , Yu Ru Huang
  • , Ka Man Chong
  • , Chun Yu Hung
  • , Zhi Long Ke
  • , Ruey Yi Chang*
  • *Corresponding author for this work
  • National Dong Hwa University
  • Chang Gung University

Research output: Contribution to journalJournal Article peer-review

24 Scopus citations

Abstract

Background: Japanese encephalitis virus (JEV) is a member of the mosquito-borne Flaviviridae family of viruses that causes human encephalitis. Upon infection of a new host, replication of viral RNA involves not only the viral RNA-dependent RNA polymerase (RdRp), but also host proteins. Host factors involved in JEV replication are not well characterized. Results: We identified Hdj2, a heat-shock protein 40 (Hsp40)/DnaJ homolog, from a mouse brain cDNA library interacting with JEV nonstructural protein 5 (NS5) encoding viral RdRp using yeast two-hybrid system. Specific interaction of Hdj2 with NS5 was confirmed by coimmunoprecipitation and colocalization in JEV-infected cells. Overexpression of Hdj2 in JEV-infected cells led to an increase of RNA synthesis, and the virus titer was elevated approximately 4.5- to 10-fold. Knocking down of Hdj2 by siRNA reduced the virus production significantly. Conclusions: We conclude that Hdj2 directly associates with JEV NS5 and facilitates viral replication. This study is the first to demonstrate Hdj2 involved in JEV replication, providing insight into a potential therapeutic target and cell-based vaccine development of JEV infection.

Original languageEnglish
Article number471
JournalVirology Journal
Volume8
DOIs
StatePublished - 2011

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Hdj2
  • Hsp40
  • JEV
  • and RdRp

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