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猪繁殖与呼吸综合征病毒的非结构蛋白Nsp2TF下调猪白细胞抗原I类分子的表达。

The non-structural protein Nsp2TF of porcine reproductive and respiratory syndrome virus down-regulates the expression of Swine Leukocyte Antigen class I.

作者信息

Cao Qian M, Subramaniam Sakthivel, Ni Yan-Yan, Cao Dianjun, Meng Xiang-Jin

机构信息

Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, United States.

Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, United States.

出版信息

Virology. 2016 Apr;491:115-24. doi: 10.1016/j.virol.2016.01.021. Epub 2016 Feb 16.

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) is arguably the most economically-important global swine pathogen. Here we demonstrated that PRRSV down-regulates Swine Leukocyte Antigen class I (SLA-I) expression in porcine alveolar macrophages, PK15-CD163 cells and monocyte-derived dendritic cells. To identify the viral protein(s) involved in SLA-I down-regulation, we tested all 22 PRRSV structural and non-structural proteins and identified that Nsp1α and Nsp2TF, and GP3 significantly down-regulated SLA-I expression with Nsp2TF showing the greatest effect. We further generated a panel of mutant viruses in which the Nsp2TF protein synthesis was abolished, and found that the two mutants with disrupted -2 ribosomal frameshifting elements and additional stop codons in the TF domain were unable to down-regulate SLA-I expression. Additionally we demonstrated that the last 68 amino acids of TF domain in Nsp2TF are critical for this function. Collectively, the results indicate a novel function of Nsp2TF in negative modulation of SLA-I expression.

摘要

猪繁殖与呼吸综合征病毒(PRRSV)可以说是全球对猪经济影响最为重大的病原体。在此,我们证明PRRSV可下调猪肺泡巨噬细胞、PK15-CD163细胞和单核细胞来源的树突状细胞中猪白细胞抗原I类(SLA-I)的表达。为了鉴定参与SLA-I下调的病毒蛋白,我们检测了PRRSV的所有22种结构蛋白和非结构蛋白,发现Nsp1α、Nsp2TF和GP3可显著下调SLA-I的表达,其中Nsp2TF的作用最为明显。我们进一步构建了一组突变病毒,其中Nsp2TF蛋白的合成被阻断,发现两个在TF结构域中-2核糖体移码元件被破坏且含有额外终止密码子的突变体无法下调SLA-I的表达。此外,我们证明Nsp2TF中TF结构域的最后68个氨基酸对于该功能至关重要。总体而言,这些结果表明Nsp2TF在负向调节SLA-I表达方面具有新功能。

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