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Matrine displayed antiviral activity in porcine alveolar macrophages co-infected by porcine reproductive and respiratory syndrome virus and porcine circovirus type 2

机译:苦参碱在猪肺泡巨噬细胞中被猪繁殖与呼吸综合征病毒和猪圆环病毒2型共感染显示抗病毒活性

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摘要

The co-infection of porcine reproductive respiratory syndrome virus (PRRSV) and porcine circovirus type 2 (PCV2) is quite common in clinical settings and no effective treatment to the co-infection is available. In this study, we established the porcine alveolar macrophages (PAM) cells model co-infected with PRRSV/PCV2 with modification in vitro, and investigated the antiviral activity of Matrine on this cell model and further evaluated the effect of Matrine on virus-induced TLR3,4/NF-κB/TNF-α pathway. The results demonstrated PAM cells inoculated with PRRSV followed by PCV2 2 h later enhanced PRRSV and PCV2 replications. Matrine treatment suppressed both PRRSV and PCV2 infection at 12 h post infection. Furthermore, PRRSV/PCV2 co- infection induced IκBα degradation and phosphorylation as well as the translocation of NF-κB from the cytoplasm to the nucleus indicating that PRRSV/PCV2 co-infection induced NF-κB activation. Matrine treatment significantly down-regulated the expression of TLR3, TLR4 and TNF-α although it, to some extent, suppressed p-IκBα expression, suggesting that TLR3,4/NF-κB/TNF-α pathway play an important role of Matrine in combating PRRSV/PCV2 co-infection. It is concluded that Matrine possesses activity against PRRSV/PCV2 co-infection in vitro and suppression of the TLR3,4/NF-κB/TNF-α pathway as an important underlying molecular mechanism. These findings warrant Matrine to be further explored for its antiviral activity in clinical settings.
机译:猪繁殖性呼吸综合征病毒(PRRSV)和2型猪圆环病毒(PCV2)的共同感染在临床环境中非常普遍,尚无有效的联合感染治疗方法。在这项研究中,我们建立了与PRRSV / PCV2共感染并经修饰的猪肺泡巨噬细胞(PAM)细胞模型,并研究了苦参碱对该细胞模型的抗病毒活性,并进一步评估了苦参碱对病毒诱导的TLR3的作用,4 /NF-κB/TNF-α途径。结果表明,接种PRRSV的PAM细胞后再接种PCV2 2h,可增强PRRSV和PCV2的复制。苦参碱治疗在感染后12h抑制PRRSV和PCV2感染。此外,PRRSV / PCV2共感染诱导IκBα降解和磷酸化,以及NF-κB从细胞质向细胞核移位,表明PRRSV / PCV2共感染诱导NF-κB活化。苦参碱治疗显着下调了TLR3,TLR4和TNF-α的表达,尽管在一定程度上抑制了p-IκBα的表达,这表明TLR3,4 /NF-κB/TNF-α途径在苦参碱中起重要作用。与PRRSV / PCV2共感染。结论:苦参碱在体外具有抗PRRSV / PCV2共感染的活性,并抑制TLR3,4 /NF-κB/TNF-α通路是重要的潜在分子机制。这些发现保证了苦参碱在临床环境中的抗病毒活性有待进一步研究。

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