ZIKV NS5-mediated STAT2 degradation as a determinant of immune evasion and pathogenicity

Zhang, Y.; Liu, C.; Li, C.; Guo, Y.; Bai, L.; Wang, P.; An, J.; Liu, W. J.; Ding, Q.

doi:10.64898/2025.12.28.696729

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bioRxiv · 10.64898/2025.12.28.696729

ZIKV NS5-mediated STAT2 degradation as a determinant of immune evasion and pathogenicity

Zhang, Y.·Liu, C.·Li, C.·Guo, Y.·Bai, L.·Wang, P.·An, J.·Liu, W. J.·Ding, Q.

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Abstract

Type I interferon (IFN) signaling is a central antiviral defense, with STAT2 driving the expression of IFN-stimulated genes (ISGs) to restrict viral infection. Many flaviviruses, including Zika virus (ZIKV), evade this pathway through non-structural protein 5 (NS5)-mediated ubiquitination and proteasomal degradation of STAT2, yet the contribution of this immune evasion strategy to viral fitness and pathogenesis remains incompletely defined. Here, using a multi-step mutational scanning strategy that jointly assessed STAT2 degradation and viral RNA replication, we identified a single NS5 residue, L162, as uniquely permissive to substitution that abolishes STAT2 degradation without compromising intrinsic replication functions. Substitution of L162 with alanine or glycine (L162A or L162G) selectively disrupted NS5 recruitment of the ZSWIM8-CUL3 E3 ubiquitin ligase, thereby preserving STAT2 stability and restoring IFN signaling. Recombinant ZIKV carrying these mutations exhibited reduced replication and enhanced ISG induction in human cells, defects fully rescued by STAT2 knockout. In A129 mice (type I IFN receptor deficient), mutant and WT viruses replicated comparably, but in human STAT2 knock-in mice, ZIKV-NS5L162G exhibited markedly reduced viral loads and disease. Notably, infection with ZIKV-NS5L162G elicited robust neutralizing antibody and T cell responses that conferred protection against WT challenge. Together, these findings establish NS5-mediated STAT2 degradation as a central determinant of ZIKV immune evasion, viral fitness and pathogenesis, and highlight disruption of NS5-STAT2 antagonism as a promising strategy for antiviral intervention and rational attenuation.

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Zhang, Y., Liu, C., Li, C., Guo, Y., Bai, L., Wang, P., An, J., Liu, W. J., Ding, Q.. 2025-12-29. ZIKV NS5-mediated STAT2 degradation as a determinant of immune evasion and pathogenicity. https://doi.org/10.64898/2025.12.28.696729

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