Abstract

Japanese Encephalitis Virus (JEV), a globally important pathogen, belongs to the family Flaviviridae, is transmitted between vertebrate hosts by mosquitoes, principally by Culex tritaeniorhynchus. The E-glycoprotein of the virus mediates its attachment to the host cell receptors. In this study, we cloned and purified JEV E-glycoprotein in pET28a vector using E. coli BL21 (DE3) cells. A pull down assay was performed using plasma membrane fraction of BALB/c mouse brain and E-glycoprotein as a bait protein. 2-Dimensional Gel Electrophoresis based separation of the interacting proteins was analyzed by mass spectrometry. Among all the identified partners of E-glycoprotein, PLVAP (Plasmalemma vesicle associated protein) and GKN3 (Gastrokine3) showed significant up-regulation in both JEV infected mouse brain and neuro2a cells. In-silico studies also predicted significant interaction of these receptors with E-glycoprotein. Additionally, overexperssion and silencing of these receptors resulted in increase and reduction in viral load respectively, suggesting them as two critical cellular receptors governing JEV entry and propagation in neurons. In support, we observed significant expression of PLVAP but not GKN3 in post-mortem autopsied human brain tissue. Our results establish two novel receptor proteins in neurons in case of JEV infection, thus providing potential targets for antiviral research.

Highlights

  • Japanese Encephalitis Virus (JEV), a globally important pathogen, belongs to the family Flaviviridae, is transmitted between vertebrate hosts by mosquitoes, principally by Culex tritaeniorhynchus

  • Affinity pull down analysis was performed using JEV E-glycoprotein of GP78 strain as a bait protein to identify the interacting proteins in the mouse brain membrane

  • 1 mg of membrane protein was incubated with 5 mg of purified

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Summary

Introduction

Japanese Encephalitis Virus (JEV), a globally important pathogen, belongs to the family Flaviviridae, is transmitted between vertebrate hosts by mosquitoes, principally by Culex tritaeniorhynchus. The. E-glycoprotein of the virus mediates its attachment to the host cell receptors. Among all the identified partners of E-glycoprotein, PLVAP (Plasmalemma vesicle associated protein) and GKN3 (Gastrokine3) showed significant up-regulation in both JEV infected mouse brain and neuro2a cells. 1% of the virus infected human population develops encephalitis symptoms; out of which 20–30% cases are fatal while. JEV infection in a host requires interaction of viral attachment proteins and cellular membrane proteins. The 52 kDa JEV–E glycoprotein mediates viral attachment to the host cell membrane proteins followed by membrane fusion. DIII mediates the main interaction of the E-glycoprotein with the host cell membrane. Immunoglobulin like domain DIII is reported to play a major role in membrane protein interaction in cases of Dengue and Tick borne encephalitis viruses[4,5]

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