4.6 Article

Mapping the Key Residues within the Porcine Reproductive and Respiratory Syndrome Virus nsp1α Replicase Protein Required for Degradation of Swine Leukocyte Antigen Class I Molecules

Journal

VIRUSES-BASEL
Volume 14, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/v14040690

Keywords

porcine reproductive and respiratory syndrome virus (PRRSV); nonstructural protein 1 alpha (nsp1 alpha); swine leukocyte antigen class I (SLA-I); degradation; reverse genetics; immune escape

Categories

Funding

  1. National Natural Science Foundation of China [32025035, 31490603]
  2. China Postdoctoral Science Foundation [2020M680773]
  3. China Agriculture Research System [CARS-35]
  4. Chinese ministry of Agriculture and Rural Affairs

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This study identifies critical residues within the nonstructural protein 1 alpha of the porcine reproductive and respiratory syndrome virus (PRRSV), providing insights into how the virus is able to evade host immunity.
The nonstructural protein 1 alpha (nsp1 alpha) of the porcine reproductive and respiratory syndrome virus (PRRSV) has been shown to target swine leukocyte antigen class I (SLA-I) for degradation, but the molecular details remain unclear. In this report, we further mapped the critical residues within nsp1 alpha by site-directed mutagenesis. We identified a cluster of residues (i.e., Phe17, Ile81, Phe82, Arg86, Thr88, Gly90, Asn91, Phe94, Arg97, Thr160, and Asn161) necessary for this function. Interestingly, they are all located in a structurally relatively concentrated region. Further analysis by reverse genetics led to the generation of two viable viral mutants, namely, nsp1 alpha-G90A and nsp1 alpha-T160A. Compared to WT, nsp1 alpha-G90A failed to co-localize with either chain of SLA-I within infected cells, whereas nsp1 alpha-T160A exhibited a partial co-localization relationship. Consequently, the mutant nsp1 alpha-G90A exhibited an impaired ability to downregulate SLA-I in infected macrophages as demonstrated by Western blot, indirect immunofluorescence, and flow cytometry analysis. Consistently, the ubiquitination level of SLA-I was significantly reduced in the conditions of both infection and transfection. Together, our results provide further insights into the mechanism underlying PRRSV subversion of host immunity and have important implications in vaccine development.

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