A Japanese encephalitis virus biological clone with angene point mutation exhibitsandattenuation of neurovirulence.

Abstract

The Japanese encephalitis virus (JEV), a leading cause of viral encephalitis, exists as similar but non-identical biological clones whose genomic variations/mutations may determine neurovirulence. Two biological clones purified from a brain-derived, clinical isolate were testedfor neurovirulence using human neuronal cells (SK-N-MC) and mouse neuronal cells (NIE-115) andon a footpad-inoculation mouse model. One clone (JEV-M) demonstrated significantly reduced infectivity in both neuronal cells and the mouse model compared to another clone (JEV-V). Of the 2gene point mutations in JEV-M, only the T175C mutation, which translates as an E protein residue 59, amino acid tyrosine to histidine change (Y59H), was found to be the neurovirulence determinant as confirmed by testing with infectious clones with or without these mutations. These novel findings could further our understanding of JEV neuropathogenesis and may be useful for future vaccine development.