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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*
  • *此作品的通信作者
  • National Dong Hwa University
  • Chang Gung University

研究成果: 期刊稿件文章同行評審

24 引文 斯高帕斯(Scopus)

摘要

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.

原文英語
文章編號471
期刊Virology Journal
8
DOIs
出版狀態已出版 - 2011

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