Understanding the interaction of hepatitis C virus with host DEAD-box RNA helicases

Figure 3 Analysis of viral replication and viral infectivity following knockdown of endogenous DDX5, DDX3 and DDX6 in Huh7. 5 cells. Cells transfected with DDX5 short interfering RNA (siRNA) in parallel with a control siRNA, DDX3 siRNA and DDX6 siRNA. At 48 h, cells were infected with J6/JFH-1(p47) hepatitis C virus (HCV) at an multiplicity of infection of 2. A: At 2 and 4 d.p.i., the total RNA was isolated from the cells, reverse transcribed, and the resulting cDNA was subjected to quantitative polymerase chain reaction for detection of genomic HCV RNA and glyceraldehyde-3-phosphate dehydrogenase mRNA as previously described[73]; B: Virus supernatants collected 2 and 4 d.p.i. were titrated on naive Huh7.5 cells by using indirect immunofluorescence as previously described[74] and expressed as focus forming units per millilitre (mL). Statistical analysis was performed using the two-tailed Student’s t test to determine if the differences between the gene specific siRNA-treated and control siRNA-treated cells were statistically significant. ^bP < 0.01 vs control siRNA-treated cells. Data were obtained from three independent experiments and one representative set of data is shown. Each measurement was performed in triplicate, and the average (± SD) is presented.