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Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV
Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV
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Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV
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Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV
Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV

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Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV
Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV
Journal Article

Phospholipase PLA2G16 Accelerates the Host Interferon Signaling Pathway Response to FMDV

2025
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Overview
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.