An intact primordial interferon antiviral signalling network in amphioxus illuminates the basal chordate origin of vertebrate IFN immunity
The evolutionary origin of the complete interferon (IFN) antiviral signalling cascade across chordates has long remained elusive, as fully functional IFN machinery had not been biochemically reconstituted in basal cephalochordates. Here we combine phylogenetics, AlphaFold3 structural prediction, multi-omic profiling and a full panel of in vitro and in vivo functional assays to characterize an intact primordial IFN network in amphioxus Branchiostoma japonicum, the extant sister group of all vertebrates. Amphioxus encodes a pair of undifferentiated BjTBK1/IKK{varepsilon} paralogs that form cytoplasmic heterodimers, whose conserved kinase-domain phosphorylation residues are mandatory for downstream IRF-driven IFN promoter activation. Despite minimal primary sequence homology with vertebrate IFNs, BjIFN1/2 possess compact -helical core folds that hint at potential structural analogy to vertebrate mucosal type III IFN-{lambda}. We identify two primitive class II cytokine receptors BjCRFB1 and BjCRFB2 that act as functional IFN sensors. Phylogenetic and tertiary structural validations confirm these undiversified ancestral receptor prototypes arose before vertebrate IFN receptor subfunctionalization, and their distinct temporal induction profiles upon viral challenge closely mirror the mucosal immune surveillance orchestrated by vertebrate IFN-{lambda}-IFNLR signalling. AlphaFold3 ligand-receptor docking identifies BjIFN2-BjCRFB2 as the optimal binding pair among all tested combinations, yet all modelled complexes yield low interface scores indicative of weak ancestral intermolecular interactions. Downstream signal transduction relies on two STAT paralogs, BjSTATa and BjSTATb, which jointly mediate transcriptional activation of core antiviral effector genes. The conserved GTPase BjMx serves as a central IFN-stimulated effector to suppress viral replication and maintain tissue immune homeostasis. Collectively, our structural and functional evidence demonstrates that the full hierarchical IFN signalling apparatus was fully assembled in basal cephalochordates prior to vertebrate radiation. The amphioxus IFN cascade preserves core ancestral molecular traits including structure-dependent ligand conservation and primitive low-affinity ligand-receptor interactions. This study resolves a long-standing evolutionary gap and provides definitive functional evidence demonstrating that IFN-mediated innate immunity constitutes an ancestral chordate trait, rather than a vertebrate-specific evolutionary innovation. It also puts forward the hypothesis that mucosal surveillance may represent the ancestral mode of chordate IFN defence.