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. 2019 Aug 13;93(17):e00720-19. doi: 10.1128/JVI.00720-19

FIG 3.

FIG 3

Immunogenicity of WNV-ΔNS1. (A and B) PRNT50 assay. PRNT50 testing against both WT WNV and WNV-ΔNS1 was performed with two different neutralizing antibodies against WNV envelope, i.e., FD011-1 (A) and FD011-2 (B). Serial 2-fold dilutions of neutralizing antibodies were incubated with WT WNV or WNV-ΔNS1 viruses. The inhibition rates were calculated by defining no-antibody treatment of WT WNV (0 μg/ml) as 0%. (C) ELISA of the antisera against WNV and WNV-ΔNS1. Two independent experiments were performed in triplicate. Data represent the mean ± standard deviation of triplicate measurements in a representative experiment. The asterisks denote statistical differences between the indicated groups. *, P < 0.05; **, P < 0.01; n.s., no statistical difference.