Key result
Sodium tanshinone IIA sulfonate (STS) exhibits anti-PRRSV activity in vitro by suppressing autophagy-related genes and effectively suppressing PRRSV's N protein replication and N gene expression.
Sodium tanshinone IIA sulfonate exhibits in vitro antiviral activity against PRRSV by suppressing autophagy-related genes.
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Supports further preclinical testing of STS against PRRSV; leaves open therapeutic translation in vivo.
BACKGROUND: In previous research, we have demonstrated that sodium tanshinone IIA sulfonate (STS) has anti-porcine reproductive and respiratory syndrome virus (PRRSV) activity, but whether autophagy is involved in this process is still unknown. In this study, the autophagy effect of STS against PRRSV infection was investigated in vitro. METHODS: Quantitative real-time PCR (qRT-PCR) and western blot was used to evaluate the inhibition ability of STS on the mRNA expression levels on cell autophagy genes, that is Beclin1, ATG5 and ATG7. Simultaneously, the effect of STS on N protein/gene expression was assessed by indirect immuno-fluorescence assay (IFA), qRT-PCR and western blot. RESULTS: The results indicated that STS inhibits autophagy induced by PRRSV. In addition, STS effectively suppresses PRRSV's N protein replication and N gene expression in Marc-145 cells infected with PRRSV in a time-dependent manner. CONCLUSIONS: Our results suggest that STS exhibits anti-PRRSV activity in vitro by suppressing autophagy-related genes, which may provide a theoretical basis for further pharmacological agent development regarding PRRSV infection.
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Sun et al. (2018) studied Porcine reproductive and respiratory syndrome virus (PRRSV) infection. Sodium tanshinone IIA sulfonate (STS) was evaluated on Autophagy-related gene expression (Beclin1, ATG5, ATG7) and PRRSV N protein/gene expression. Sodium tanshinone IIA sulfonate (STS) exhibits anti-PRRSV activity in vitro by suppressing autophagy-related genes and effectively suppressing PRRSV's N protein replication and N gene expression.
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