STING-NF-κB signaling builds an influenza spillover barrier
Summary
Influenza pandemics are often traced back to the spillover of avian influenza A viruses (IAVs) to humans. However, barriers against IAV transmission remain elusive. We demonstrated human stimulator of interferon genes (STING) as a transmission barrier against IAVs. STING activated nuclear factor κB (NF-κB) and downstream NF-κB-stimulated genes (NSGs) through a specific domain. Among these NSGs, growth arrest and DNA damage-inducible protein 34 (GADD34) was crucial for IAV restriction. Some
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# STING-NF-κB signaling builds an influenza spillover barrier
*Published: 2026 Feb 26*
Influenza pandemics are often traced back to the spillover of avian influenza A
viruses (IAVs) to humans. However, barriers against IAV transmission remain
elusive. We demonstrated human stimulator of interferon genes (STING) as a
transmission barrier against IAVs. STING activated nuclear factor κB (NF-κB) and
downstream NF-κB-stimulated genes (NSGs) through a specific domain. Among these
NSGs, growth arrest and DNA damage-inducible protein 34 (GADD34) was crucial for
IAV restriction. Some IAVs have evolved to evade activating human STING by
mutating residue 115 in their matrix protein 1 (M1), which is essential for
efficient viral replication in human respiratory cells. This barrier against the
zoonotic threat of IAVs provides a tool for future investigations into the
biological functions of the cyclic guanosine monophosphate-adenosine
monosphosphate (cGMP-AMP) synthase (cGAS)-STING-NF-κB signaling pathway.
DOI: 10.1126/science.ads4405