Proximity proteomics reveals a role for IFI16 during human coronavirus infection

Abstract Viruses rely on the infected host cell to ensure successful replication and propagation of infection. This is achieved through interactions between virus-encoded proteins and proteins expressed in infected cells. All human coronaviruses (HCoVs) encode 16 non-structural proteins (NSPs) which exhibit some level of similarity in identity and function among the HCoVs. To identify host proteins that are potential interacting partners of HCoV NSPs, we utilized split-TurboID along with mass spectrometry and identified IFN-γ-inducible protein-16 (IFI16) as a proximal partner of SARS-CoV-2 NSP8 and NSP10. To investigate the significance of the association between the NSP8/NSP10 complex and IFI16, we utilized CRISPR-Cas9 to knockout and CRISPRi to knockdown IFI16 in A549 cells and demonstrated that loss or reduced expression of IFI16 leads to a decrease in human coronavirus infection. We further demonstrated that there is reduced viral RNA replication and viral protein synthesis upon loss of IFI16. Interestingly, the loss of IFI16 results in reduced expression of type I IFNs. Taken together, these data suggests that IFI16 promotes human coronavirus infection, and the role IFI16 plays in coronavirus replication is independent of its role as a regulator of type I IFN gene expression. Competing Interest Statement The authors have declared no competing interest. Abbreviations - NSP - non-structural protein - IFI16 - IFN-γ-inducible protein-16 - HCoV-OC43 - Human coronavirus OC43 - CRISPR - Clustered Regularly Interspaced Short Palindromic Repeats - CRISPRi - Clustered Regularly Interspaced Short Palindromic Repeats Interference - MOI - multiplicity of infection.