Research Paper Volume 12, Issue 14 pp 14467—14479

The regulatory role of miR-107 in Coxsackie B3 virus replication

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Figure 1. (AB) Hela cells were infected with CVB3 with specified titers at planned time points. Total RNA of the cells were extracted and miR-107 was detected using real-time PCR. (CE) Hela cells were infected at a certain concentration of CVB3, and viral replication at different time points was observed. (F) The transfection efficiency of miR-107 mimics was analyzed using RT-qPCR, and western blot reflected viral replication at a protein level. Viral titers were determined by plaque assay. (G) The transfection efficiency of miR-107 inhibitors was detected by RT-qPCR, and western blot reflected virus replicated at a protein level. Viral titers were determined by plaque assay. (H) The replication level of EGFP-Iabeled CVB3 was observed in Hela cells which had been transfected with mimics107 or 107-in (magnification, 4×).