Fig. 3.

UA does not directly damage MSRV particles. (A) Workflow of the experimental design followed in (B-C). MSRV (1 × 10³ TCID₅₀/0.1 mL) and 13.14 μM UA were incubated at 25 °C for 2 and 4 h. Subsequently, qPCR assay and viral titer were performed. (B) qRT-PCR analysis of MSRV glycoprotein (G) encoding gene. The data were shown as mean ± SEM. (C) The titers of MSRV in GCO cells. Data were shown as mean ± SEM.