4.5 Article Data Paper

Quantitative Proteomic Analysis of Global Protein Acetylation in PRRSV-Infected Pulmonary Alveolar Macrophages

Journal

PROTEOMICS
Volume 21, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1002/pmic.202000019

Keywords

acetylation; liquid chromatography‐ mass spectrometry; porcine reproductive and respiratory syndrome; post‐ translational modification; tandem mass tag

Funding

  1. Science-Technology Foundation for Outstanding Young Scientists of Henan Academy of Agricultural Sciences [2016YQ21]
  2. Earmarked Fund for Modern Agro-industry Technology Research System of China [CARS-35]
  3. Special Fund for Henan Agriculture Research System [S2012-06]

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This study identified 3731 lysine acetylation sites on 1421 cellular proteins in PRRSV-infected PAMs, indicating the involvement of these acetylated proteins in host immune responses and energy metabolism. These findings will help in understanding PRRSV pathogenesis and identifying new cellular targets for anti-PRRSV therapeutics.
Porcine reproductive and respiratory syndrome (PRRS), caused by PRRS virus (PRRSV), is a serious viral disease affecting global swine industry. Due to the lack of effective vaccines, new antiviral strategies to compensate for the inefficacy of available vaccines are urgently required. Lysine acetylation, as an important post-translational modification during infection, plays a key regulatory role in host antiviral responses. In this study, the global acetylome is profiled using acetylation specific antibody-based enrichment and tandem mass tag label high-affinity purification liquid chromatography-mass spectrometry in PRRSV-infected pulmonary alveolar macrophages (PAMs). As a result, 3731 lysine acetylation sites on 1421 cellular proteins are identified. Bioinformatics analysis of the different acetylated proteins revealed their involvement in various biological processes, including the host immune response and energy metabolism. These findings will contribute to the understanding of PRRSV pathogenesis and identify new cellular targets for anti-PPRSV therapeutics.

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