Back to Search
Start Over
The non-structural protein Nsp2TF of porcine reproductive and respiratory syndrome virus down-regulates the expression of Swine Leukocyte Antigen class I
- Source :
- Virology. 491:115-124
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
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.
- Subjects :
- 0301 basic medicine
Swine
Viral protein
Mutant
Porcine Reproductive and Respiratory Syndrome
Down-Regulation
Viral Nonstructural Proteins
medicine.disease_cause
03 medical and health sciences
Virology
Protein biosynthesis
medicine
Animals
Porcine respiratory and reproductive syndrome virus
Pathogen
chemistry.chemical_classification
Translational frameshift
biology
Histocompatibility Antigens Class I
fungi
Histocompatibility Antigens Class II
Porcine reproductive and respiratory syndrome virus
biology.organism_classification
Stop codon
Protein Structure, Tertiary
Amino acid
030104 developmental biology
chemistry
Host-Pathogen Interactions
Subjects
Details
- ISSN :
- 00426822
- Volume :
- 491
- Database :
- OpenAIRE
- Journal :
- Virology
- Accession number :
- edsair.doi.dedup.....58c85cfb1133542891e16dc7b24685b3
- Full Text :
- https://doi.org/10.1016/j.virol.2016.01.021