Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3424016 | Virology | 2016 | 10 Pages |
•Identification of a novel function of PRRSV Nsp2TF in down-regulating SLA-I.•The TF domain in Nsp2TF is critically important for SLA-I down-regulation.•Two mutants with abolished Nsp2TF expression restore SLA-I expression after infection.•Results have implications in developing PRRSV vaccines with better CMI responses.
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.