Fig. 5From: Construction of an infectious clone of Zika virus stably expressing an EGFP marker in a eukaryotic expression systemCAPE inhibition of ZIKA–EGFP infection. a Vero cells infected with ZIKA–WT and ZIKA–EGFP at a MOI of 0.1 were cultured in the presence and absence of 10 µM CAPE for 48 h, followed by detection of Zika viral E gene expression by qPCR. b Fluorescent cells were observed under a fluorescence microscope (×200). The qPCR assays were repeated three times and each group contained three replicates. ***P < 0.001, n.s., not significantBack to article page