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. 2018 Jul 18;13(7):e0200726. doi: 10.1371/journal.pone.0200726

Fig 8. Addition of exogenous prostaglandin E2 can compensate for COX-induced inhibition of feline calicivirus (FCV) and murine norovirus (MNV) replications.

Fig 8

(A–D) CRFK cells and RAW264.7 were infected with FCV (MOI, 1 FFU/ml) and MNV (MOI, 1 TCID50/ml), respectively, and then treated with noncytotoxic doses of indomethacin and NS-398 for MNV and FCV, respectively. Two doses of exogenous PGE2, 5 or 50 μM for MNV, and 2 μM or 20 μM for FCV, were then added in the maintenance media, and samples were harvested at 8 h post-infection (hpi) for FCV and 24 hpi for MNV. Viral titer and viral genome copy numbers were determined by TCID50 and quantitative real time PCR analyses and compared between mock- and drug-treated groups. The data presented are means and standard errors of the mean from three different experiments. Statistical analysis was performed using one-way analysis of variance. ** p < 0.001.