The insulin/insulin growth factor (IGF) system plays a central role in regulating metabolism and growth. We identified viral insulin/IGF1-like peptides (VILPs) in Iridoviridae and investigated their role in host-virus interactions. Using grouper iridovirus (GIV) on grouper and zebrafish cells, we show that VILPs are early viral genes and are secreted during infection. VILPs activate insulin receptor (IR) and IGF-1 receptor (IGF1R) phosphorylation and stimulate the phosphatidylinositol 3-kinase (PI3K) pathway. GIV-VILP present in the supernatants of infected cells triggers dose- and time-dependent signaling through selective interaction with IGF1R. Functionally, IR inhibition suppresses GIV replication, whereas IGF1R inhibition enhances it, and IGF-1 stimulation reduces replication. During infection, GIV-VILP competes with IGF-1, attenuating IGF1R signaling and reducing proliferation. Transcriptome analysis confirms negative regulation of cell cycle pathways. Using a zebrafish infection model, we demonstrate VILP expression and IGF-1 signaling inhibition. Our findings reveal a viral mimicry mechanism that modulates host IGF-1 signaling to promote viral replication.

Department of Biology Boston College Chestnut Hill MA USA

Department of Chemical Engineering and Bioengineering University of New Hampshire Durham NH 03824 USA

Department of Chemical Engineering and Bioengineering University of New Hampshire Durham NH 03824 USA; Department of Chemistry University of New Hampshire Durham NH 03824 USA; Integrated Applied Mathematics Program University of New Hampshire Durham NH 03824 USA; Molecular and Cellular Biotechnology Program University of New Hampshire Durham NH 03824 USA

Department of Chemistry Indiana University Bloomington IN USA

Institute of Organic Chemistry and Biochemistry Czech Academy of Sciences Prague Czech Republic

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