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Bacterial cell surface display: A method for studying Japanese encephalitis virus pathogenicity

Dou, Jianlin; Daly, Janet; Yuan, Zhiming; Jing, Tao; Solomon, Tom

Authors

Jianlin Dou

Zhiming Yuan

Tao Jing

Tom Solomon



Abstract

Infection with Japanese encephalitis virus (JEV), a mosquito-borne, neurotropic flavivirus, may cause acute encephalitis in humans. Recombinant Salmonella typhimurium BRD509 was constructed to display domain III of the envelope (E) protein of JEV (JEDIII) on its surface with the N-terminal domain of ice nucleation protein (INPN) as the display motif. Bacterial cell surface display was confirmed by Western blot analysis and immunohistochemical staining. Binding of recombinant INPN-JEDIII and JEDIII proteins to three mammalian cell lines was compared using a cell-binding ELISA; the human neuroblastoma cell line SK-N-SH, which had a low level of binding, was selected for further studies. The display of JEDIII on the surface of BRD509 did not significantly influence its invasiveness was confirmed by measuring released bacterial antigen using whole-cell ELISA. The relative expression of an apoptosis-related gene and total DNA damage were assessed to investigate the effects of infection on SK-N-SH cells. Compared to BRD509, infection with the recombinant bacterium reduced cell damage, suggesting that JEDIII may limit apoptosis during the early stages of JEV infection. Our studies demonstrated that it is feasible to study the pathogenesis of JEV using the approach described.

Citation

Dou, J., Daly, J., Yuan, Z., Jing, T., & Solomon, T. (2009). Bacterial cell surface display: A method for studying Japanese encephalitis virus pathogenicity. Japanese Journal of Infectious Diseases, 62(5), 402-408

Journal Article Type Article
Publication Date 2009
Deposit Date Apr 4, 2025
Journal Japanese Journal of Infectious Diseases
Print ISSN 1344-6304
Electronic ISSN 1884-2836
Peer Reviewed Peer Reviewed
Volume 62
Issue 5
Pages 402-408
Public URL https://nottingham-repository.worktribe.com/output/46456863