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Published on: December 29, 2015
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.
Abstract:
The pathogenesis of Japanese encephalitis virus (JEV) is complex and unclearly defined, and in particular, the effects of the JEV receptor (JEVR) on diverse susceptible cells are elusive. In contrast to previous studies investigating JEVR in rodent or mosquito cells, in this study, we used primate Vero cells instead. We noted that few novel proteins co‑immunoprecipitated with JEV, and discovered that one of these was heat shock protein 90β (HSP90β), which was probed by mass spectrometry with the highest score of 60.3 after questing the monkey and human protein databases. The specific HSP90β‑JEV binding was confirmed by western blot analysis under non‑reducing conditions, and this was significantly inhibited by an anti‑human HSP90β monoclonal antibody in a dose‑dependent manner, as shown by immunofluorescence assay and flow cytometry. In addition, the results of confocal laser scanning microscopic examination demonstrated that the HSP90β‑JEV binding occurred on the Vero cell surface. Finally, JEV progeny yields determined by plaque assay were also markedly decreased in siRNA‑treated Vero cells, particularly at 24 and 36 h post‑infection. Thus, our data indicate that HSP90β is a binding receptor for JEV in Vero cells.
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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