Viral insulin/IGF-like peptides inhibit IGF-1 receptor signaling to enhance viral replication
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
R01 DK132674
NIDDK NIH HHS - United States
R35 GM138217
NIGMS NIH HHS - United States
R35 GM146467
NIGMS NIH HHS - United States
PubMed
40829596
PubMed Central
PMC12512748
DOI
10.1016/j.celrep.2025.116149
PII: S2211-1247(25)00920-9
Knihovny.cz E-zdroje
- Klíčová slova
- CP: Metabolism, CP: Microbiology, IGF-1, IGF1R inhibition, VILP, grouper iridovirus, insulin, mimicry, zebrafish,
- MeSH
- dánio pruhované virologie MeSH
- fosforylace MeSH
- insulinu podobný růstový faktor I * metabolismus MeSH
- inzulin * metabolismus MeSH
- Iridovirus * fyziologie MeSH
- lidé MeSH
- peptidy * metabolismus MeSH
- receptor IGF typ 1 * metabolismus antagonisté a inhibitory MeSH
- receptor inzulinu metabolismus MeSH
- replikace viru * MeSH
- signální transdukce * MeSH
- virové proteiny * metabolismus genetika MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- insulinu podobný růstový faktor I * MeSH
- inzulin * MeSH
- peptidy * MeSH
- receptor IGF typ 1 * MeSH
- receptor inzulinu MeSH
- virové proteiny * MeSH
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 Chemistry Indiana University Bloomington IN USA
Institute of Organic Chemistry and Biochemistry Czech Academy of Sciences Prague Czech Republic
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