# Viral polymerase-host interaction analysis reveals that the association between avian NUP93 and PB1 promotes H5N6 avian influenza virus replication

## TL;DR

This study identifies host proteins that interact with H5N6 avian influenza virus polymerase, revealing that avian NUP93 enhances viral replication by interacting with PB1.

## Contribution

The study identifies avian NUP93 as a novel host protein that interacts with PB1 to promote H5N6 avian influenza virus replication.

## Key findings

- 455 H5N6-chicken interacting proteins were identified, with 231 successfully cloned.
- Nine host genes promote and 20 inhibit avian influenza virus proliferation in DF-1 cells.
- Avian NUP93 interacts with viral PB1 protein to enhance polymerase activity and viral proliferation.

## Abstract

The H5N6 avian influenza virus, a highly pathogenic strain, poses a significant threat to poultry production and public health. The RNA-dependent RNA polymerase (comprising PB1, PB2, and PA proteins) and nucleoprotein of highly pathogenic avian influenza viruses interact with avian host proteins, influencing the efficiency of viral RNA synthesis and severity of infection. To comprehensively understand how H5N6 avian influenza virus interfaces with host cellular mechanisms during infection and replication, it is essential to identify which host proteins physically associate with viral polymerase proteins. In this study, affinity purification mass spectrometry was used to identify physical interactions between H5N6-JX polymerase proteins (PB1, PB2, PA, and nucleoprotein) and host proteins in chicken DF-1 cells. We identified 455 H5N6-chicken interacting proteins and successfully cloned 231 of these genes. Overexpression experiments revealed several host proteins involved in viral replication in DF-1 cells. Specifically, nine host genes were found to promote avian influenza virus proliferation, whereas 20 inhibited it. Furthermore, we demonstrated that avian NUP93 interacts with the viral PB1 protein, enhancing polymerase transcriptional activity and promoting viral proliferation. These findings provide a more comprehensive understanding of how host mechanisms are manipulated during H5N6 avian influenza viral infection and replication, providing insights into the mechanisms of avian influenza virus cross-species transmission.

The RNA-dependent interaction of RNA polymerase with avian host protein determines the efficiency of viral RNA synthesis and the severity of infection. However, the strain-specific interactions of the avian influenza virus (AIV) remain unclear. In this study, we identified 455 H5N6-chicken interacting proteins and successfully cloned 231 of them. Nine host genes that promote the proliferation of avian influenza virus and 20 host genes that inhibit the proliferation of avian influenza virus were identified through overexpression experiments. In addition, we demonstrated that avian NUP93 interacts with viral PB1 protein to enhance polymerase transcriptional activity and promote viral proliferation. This study contributes to a more comprehensive and detailed understanding of the molecular mechanisms of host utilization during the H5N6 highly pathogenic avian influenza virus infection and replication.