Heat shock protein 90β in the Vero cell membrane binds Japanese encephalitis virus

Yuan Wang1, Yan Li1, Tianbing Ding1

  • 1Department of Microbiology, The Fourth Military Medical University, Xi'an, Shaanxi 710032, P.R. China.

Insights

Heat shock protein 90β (HSP90β) acts as a Japanese encephalitis virus (JEV) receptor on primate Vero cells. Inhibiting HSP90β significantly reduces JEV binding and progeny yield, clarifying JEV pathogenesis.

Area of Science:

  • Virology
  • Cell Biology
  • Molecular Biology

Background:

  • Japanese encephalitis virus (JEV) pathogenesis and receptor interactions remain incompletely understood.
  • Previous studies on JEV receptors primarily used rodent or mosquito cells, leaving primate cell interactions unclear.

Purpose of the Study:

  • To identify the JEV receptor in primate Vero cells.
  • To elucidate the role of heat shock protein 90β (HSP90β) in JEV infection.

Main Methods:

  • Mass spectrometry to identify JEV-interacting proteins in Vero cells.
  • Western blot, immunofluorescence, and flow cytometry to confirm HSP90β-JEV binding.
  • RNA interference (siRNA) to assess the impact of HSP90β on JEV replication.

Main Results:

  • Heat shock protein 90β (HSP90β) was identified as a JEV-binding protein in Vero cells.
  • HSP90β-JEV binding occurred on the cell surface and was inhibited by an anti-HSP90β antibody.
  • siRNA-mediated knockdown of HSP90β significantly reduced JEV progeny yields.

Conclusions:

  • Heat shock protein 90β (HSP90β) functions as a binding receptor for Japanese encephalitis virus (JEV) in primate Vero cells.
  • Targeting HSP90β may offer a novel strategy for controlling JEV infections.

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