Viruses (Jun 2025)

Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV

  • Bingjie Sun,
  • Xiaodong Qin,
  • Taoqing Zhang,
  • Sujie Dong,
  • Yinbo Ye,
  • Changying Wang,
  • Yan Zhang,
  • Rongzeng Hao,
  • Yi Ru,
  • Hong Tian,
  • Haixue Zheng

DOI
https://doi.org/10.3390/v17070883
Journal volume & issue
Vol. 17, no. 7
p. 883

Abstract

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PLA2G16 is a member of the phospholipase A2 family that catalyzes the generation of lysophosphatidic acids (LPAs) and free fatty acids (FFAs) from phosphatidic acid. Previously, PLA2G16 was found to be a host factor for picornaviruses. Here, we discovered that the Foot-and-Mouth Disease Virus (FMDV) infection led to an elevation in PLA2G16 transcription. We established PLA2G16 overexpression and knockdown cell lines in PK-15 cells to investigate the potential role of PLA2G16 in FMDV infection. Our findings revealed that during FMDV infection, PLA2G16-overexpressing cells had increased levels of phosphorylated STAT1 and the interferon-stimulating factors ISG15 and ISG56. In PLA2G16-overexpressing cells, p-STAT1 was observed at higher levels and earlier than in wild-type cells. Subsequent research demonstrated that PLA2G16 specifically promoted an antiviral innate immune response against FMDV. The host could detect the early release of FMDV viral nucleic acid in PLA2G16-overexpressing cells and trigger the interferon signaling pathway. Additionally, we discovered that the supernatants of PLA2G16-overexpressing cells stimulated the production of higher levels of ISG56 and phosphorylated STAT1. This suggests that PLA2G16-overexpressing cells can activate the innate immune pathway of uninfected cells after FMDV infection.

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