It is shown that integrating protein-protein interaction information derived from a protein language model boosts the discovery of vaccinia virus-host interactions, and proposes ICARus – a positive-unlabelled read-out refinement framework to achieve this.
Abstract
Recent mpox outbreaks highlight the necessity to understand the interactions between poxviruses and the human host. These can be discovered systematically through screening for host genes involved in infection at the single-cell level using RNA interference. However, off-target effects and assay noise obscure true gene-phenotype relationships, hampering the discovery of therapeutically relevant targets. Here, we show that integrating protein-protein interaction information derived from a protein language model boosts the discovery of vaccinia virus-host interactions. We propose ICARus – a positive-unlabelled read-out refinement framework to achieve this. Our approach enhances the identification of human genes with potential antiviral function. We provide the raw and refined read-outs of a genome-wide screen for vaccinia virus host factors as an agentic-AI-enabled community resource. Our findings provide a generalisable strategy for robust hit prioritisation in functional screens, accelerating discovery across complex biological systems.
It is demonstrated that genetically encoded, site-specific photo-crosslinking enables selective capture of transient interactions that are often missed by nonspecific 254 nm UV crosslinking approaches and highlights Orf3a as a multifunctional protein that engages diverse host pathways.
Eryn Lundrigan, Noreen Ahmed, J. P. Pezacki· Protein engineering, design...· 0 citations
A virus-driven proximity proteomics framework is presented to investigate immediate-early phase virus-host interactions in an authentic infection context and identifies p400 as a poised host restriction factor and establishes a temporally resolved proximity proteomics strategy transferable to other immediate-early vira...
Tanner M. Tessier, Katelyn M. MacNeil, O. B. Scudero et al.· bioRxiv· 0 citations
It is found that the mutations induce distinct transcriptional and translational alterations: rN-Alpha drives a stealth-like infection characterized by sustained translation efficiency and specific evasion of the 2’-5’-oligoadenylate synthetase (OAS) innate immune sensor, whereas rN-Delta and rN-BA trigger a highly ele...
J. Berger, Jonas Schröder, Timothy K. Soh et al.· bioRxiv· 0 citations
Viruses shape microbial metabolism through auxiliary viral genes (AVGs) that reprogram host metabolism, physiology, and gene regulation during infection. Identifying AVGs is complicated by ambiguous viral versus cellular assignment, inconsistent curation, and reliance on sequence homology that misses divergent function...
James C. Kosmopoulos, Cody Martin, J. Wainaina et al.· bioRxiv· 0 citations
This study is the first to identify circ-INSR as a host factor contributing to influenza virus replication, and provides a basis for developing circRNA-based strategies against H9N2 avian influenza virus.
A large-scale mining of the MetaVR database is presented to identify phages targeting human bacterial pathogens, establishing a large-scale framework for connecting human bacterial pathogens to phages and their lytic machinery, and translates large-scale viral genomic data into a resource for developing new therapeutic...
Mateus B. Fiamenghi, N. Kyrpides· bioRxiv· 0 citations
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