Fig 10.
Identification of the key region essential for SHFL antiviral inhibitory effect on PRRSV. PRRSV replicon (1 μg) was cotransfected with SHFL or its mutant plasmids (0.5 μg) in HEK-293T and BHK-21 cells. At 24 hpt, cell supernatants were harvested for the GLuc assay (A and C) and cell lysates for Western blot (B and D) using an anti-FLAG antibody to detect SHFL mutant expression and an anti-nsp9 antibody to detect RNA replication. β-Tubulin was detected as a loading control. Data are presented as means ± SD from three replicates. Statistical significance was analyzed using the two-tailed unpaired Student’s t-test. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001; ns, not significant.
