# Poxvirus H5 mediates the formation of liquid-liquid phase separation condensates which promote virus factory assembly

## TL;DR

The vaccinia virus H5 protein forms liquid-like clusters that help build viral replication factories, and phosphorylation is key to this process.

## Contribution

Discovery of a conserved regulatory mechanism in poxviruses involving H5 phosphorylation and LLPS for replication factory assembly.

## Key findings

- H5 forms LLPS condensates via its intrinsically disordered region, aiding viral replication.
- Phosphorylation at S127 and S130 is critical for H5-DNA interaction and LLPS formation.
- Disrupting these phosphorylation sites impairs viral replication without affecting H5 synthesis or localization.

## Abstract

Liquid-liquid phase separation (LLPS) is a fundamental mechanism for the formation of membrane-less organelles, enabling cells to compartmentalize biochemical processes without membrane boundaries. In viral infections, LLPS is increasingly recognized as a strategy for organizing replication and transcriptional machinery. Here, we report that H5, a DNA-binding protein of vaccinia virus (VACV) could undergo LLPS through its N-terminal intrinsically disordered region (IDR). H5 forms dynamic and reversible condensates in both transfected and vacv infected cells, a property also observed with H5 orthologs from mpox virus and lumpy skin disease virus. Fluorescence recovery after photobleaching (FRAP) assays confirmed the liquid-like behavior of H5 condensates. Using structure-guided mutagenesis and phosphoproteomics, we identified two critical phosphorylation sites within the IDR, S127 and S130, which are essential for the interaction between H5 and DNA. These modifications are mediated redundantly by host proteins and viral B1 kinases. Mutations at these residues inhibit the binding of H5 to DNA, thereby directly or indirectly abolish LLPS formation, and impair viral replication factory assembly, leading to a marked reduction in viral DNA replication and progeny production, without affecting the synthesis of H5 or its subcellular localization. Our findings indicate that these two serine residues of H5 contribute to its interaction with DNA and the formation of LLPS, a process that may help organize viral replication compartments and facilitate interactions with key components of the DNA polymerase complex. This study uncovers a previously uncharacterized mechanism by which the poxvirus H5 protein promotes viral factory assembly and coordinates replication, and identifies a conserved regulatory axis that may serve as a potential therapeutic target across poxvirus species.

In this study, we investigate the role of a protein called H5 from the vaccinia virus in the formation of structures inside infected cells known as viral factories. These viral factories are essential for the virus to replicate efficiently. We found that a specific region of the H5 protein enables it to form condensates with LLPS properties. These dense, liquid-like clusters may facilitate the organization of viral components and are critical for viral replication. By altering specific amino acids in H5, we were able to disrupt its ability to form these condensates, which severely affected the virus’s ability to replicate without changing how the protein is made or where it is located in the cell. Our research shows that phosphorylation of H5, a chemical modification, is crucial for its ability to form these condensates and support viral replication. This work opens new avenues for understanding how viruses manipulate cellular processes and provides potential targets for developing antiviral therapies aimed at preventing viral replication by interfering with H5–DNA binding and H5-mediated LLPS.