School of Veterinary Medicine & Biomedical Sciences, University of Nebraska-Lincoln, NE 68583, USA.
Virology. 2010 Oct 25;406(2):270-9. doi: 10.1016/j.virol.2010.07.016. Epub 2010 Aug 11.
The objective of this study was to identify porcine reproductive and respiratory syndrome virus (PRRSV)-encoded proteins that are responsible for the inhibition of TNF-α expression and the mechanism(s) involved in this phenomenon. Using a TNF-α promoter reporter system, the non-structural protein 1 (Nsp1) was found to strongly suppress the TNF-α promoter activity. Such inhibition takes place especially at the promoter's proximal region. Both Nsp1α and Nsp1β, the two proteolytic fragments of Nsp1, were shown to be involved in TNF-α promoter suppression. Furthermore, using reporter plasmids specific for transcription factors (TFs) that bind to TNF-α promoter, Nsp1α and Nsp1β were demonstrated to inhibit the activity of the TFs that bind CRE-κB(3) and Sp1 elements respectively. Subsequent analyses showed that Nsp1α moderately inhibits NF-κB activation and that Nsp1β completely abrogates the Sp1 transactivation. These findings reveal one of the important mechanisms underlying the innate immune evasion by PRRSV during infection.
本研究旨在确定猪繁殖与呼吸综合征病毒(PRRSV)编码的蛋白,这些蛋白负责抑制 TNF-α 的表达,并阐明相关的作用机制。利用 TNF-α 启动子报告系统,发现非结构蛋白 1(Nsp1)可强烈抑制 TNF-α 启动子活性。这种抑制作用主要发生在启动子的近端区域。Nsp1 的两个蛋白水解片段 Nsp1α 和 Nsp1β 均参与了 TNF-α 启动子抑制。此外,利用与结合 TNF-α 启动子的转录因子(TFs)特异性报告质粒,证明 Nsp1α 抑制结合 CRE-κB(3) 和 Sp1 元件的 TFs 的活性,而 Nsp1β 则完全阻断 Sp1 的反式激活。进一步的分析表明,Nsp1α 可适度抑制 NF-κB 的激活,而 Nsp1β 则完全阻断 Sp1 的转激活作用。这些发现揭示了 PRRSV 在感染过程中逃避固有免疫的重要机制之一。