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. 2008 Sep 18;33(2):168–173. doi: 10.1016/j.ijantimicag.2008.07.013

Fig. 2.

Fig. 2

Elucidation of a single replicative cycle of Japanese encephalitis virus in porcine stable kidney (PS) cells. PS cells were infected with a multiplicity of infection (MoI) of 1 of JEV at the 0 h time point. Virus yield in the supernatant and JEV antigen in the cells were examined at 2-h intervals up to 24 h post infection. (A) Yield of virus in the supernatant fluid. The x-axis represents the various time points at which virus yield was evaluated and the y-axis represents the virus yield (log 50% tissue culture infective dose (TCID50)/mL). (B) Detection of JEV-specific antigen using an immunofluorescence assay. It can be observed that the earliest appearance of cell-bound antigen was at 10 h post infection, whilst the earlier time points were negative for viral antigen (400×).