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首页> 外文期刊>Scientific reports. >Matrine displayed antiviral activity in porcine alveolar macrophages co-infected by porcine reproductive and respiratory syndrome virus and porcine circovirus type 2
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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:苦参碱显示猪肺泡巨噬细胞的抗病毒活性,由猪生殖和呼吸综合征病毒和猪胃肠病毒2型

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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:猪生殖呼吸道综合征病毒(PRRSV)和猪胃肠病毒2(PCV2)的共同感染在临床环境中非常常见,并且没有有效地治疗相应的共感染。在这项研究中,我们建立了在体外改性的猪肺泡巨噬细胞(PAM)细胞模型与PRRSV / PCV2进行了改性,并研究了该细胞模型对苦参碱的抗病毒活性,并进一步评估了苦参碱对病毒诱导的TLR3对病毒的影响,4 / NF-κB/ TNF-α途径。结果证明了PAM细胞接种PRRSV,其次是PCV2 2ΔH以后增强PRRSV和PCV2复制。苦参碱治疗抑制了PRRSV和PCV2感染后的感染后的感染。此外,PRRSV / PCV2有关诱导IκBα的劣化和磷酸化以及从细胞质到细胞核的NF-κB的易位,表明PRRSV / PCV2共感染诱导的NF-κB活化。苦参碱治疗显着下调TLR3,TLR4和TNF-α的表达,但在某种程度上抑制了P-IκBα表达,表明TLR3,4 / NF-κB/ TNF-α途径在苦参碱中发挥着重要作用打击PRRSV / PCV2共感染。得出结论,苦参碱具有针对PRRSV / PCV2共有的活性,并抑制TLR3,4 / NF-κB/ TNF-α途径作为重要的潜在的分子机制。这些调查结果需要在临床环境中进一步探索其抗病毒活性的矩阵。

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