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Viruses depend on their hosts for completing their life cycle, and a better understanding of virus replication can inform therapeutic strategies. Using the Orsay virus- experimental platform, we identified by a forward genetic screen the host gene (renamed ) as a novel host factor critical for Orsay virus replication. Three distinct mutations of each resulted in a >1,000-fold reduction in Orsay viral load, demonstrating a pro-viral function of had no previously described function in , but in the absence of viral infection, deletion of the locus by CRISPR/Cas9 led to a reduction in brood size and a shortened lifespan. VIRO-9 contains a ensitivity to ed light educed (SRR1) protein domain. While SRR1 domains are present in diverse organisms, including plants, yeast, and mammals, little is known about their function. The ortholog of , , can functionally complement the defect, demonstrating that the pro-viral function of the SRR1 domain is conserved over at least 80 million years of evolution. Furthermore, we identified three conserved amino acid residues within the SRR1 domain that are required for Orsay virus infection. This study provides the first insights into amino acids necessary for functionality of the SRR1 domain and demonstrates the essential role of in virus infection.IMPORTANCEHost factors required for viral replication could serve as therapeutic targets for various viral species. The Orsay virus experimental system offers a platform for identifying genes important for virus infection in nematodes that may also be important for human-infecting viruses. We determined that , a previously uncharacterized gene in containing the SRR1 domain, is required for Orsay virus replication. The related gene in , a relative of that diverged about 80 million years ago, can substitute for , demonstrating that this protein's ability to promote virus replication is functionally conserved. Because SRR1 domain-containing proteins exist in nematodes, fungi, , plants, and mammals, including humans, these proteins could be important for facilitating virus infection in other organisms as well.
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http://dx.doi.org/10.1128/jvi.00521-25 | DOI Listing |
Phytochemistry
September 2025
Équipe "Chimie des substances naturelles" BioCIS, CNRS, Université Paris-Saclay, 17, avenue des Sciences, 91400, Orsay, France. Electronic address:
Throughout the past decades, annonaceous plants have been of particular interest to the natural product community because of their therapeutic value and their richness in isoquinoline alkaloids. Taking advantage from our laboratory historical collection of these compounds, a MS/MS database of 322 isoquinolines and other metabolites from Annonaceae was implemented and named IQAMDB . The present report describes the dereplication of known alkaloids from stem barks of Greenwayodendron suaveolens (Engl.
View Article and Find Full Text PDFJ Med Virol
September 2025
School of Public Health (Shenzhen), Sun Yat-sen University, Shenzhen, Guangdong, China.
Tyrosine kinase non-receptor2 (TNK2) is a host protein involved in vesicular trafficking, cell spreading, migration, survival, and proliferation. TNK2 has been identified as a conserved host factor for the entry of several non-enveloped RNA viruses, such as Orsay virus in Caenorhabditis elegans and multiple picornaviruses in cells and mice. Although TNK2 was reported as required for influenza A virus infection in a genome-wide CRISPR screen, its role remains contentious as it was not identified in other screens.
View Article and Find Full Text PDFJ Virol
September 2025
Department of Molecular Microbiology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri, USA.
Viruses depend on their hosts for completing their life cycle, and a better understanding of virus replication can inform therapeutic strategies. Using the Orsay virus- experimental platform, we identified by a forward genetic screen the host gene (renamed ) as a novel host factor critical for Orsay virus replication. Three distinct mutations of each resulted in a >1,000-fold reduction in Orsay viral load, demonstrating a pro-viral function of had no previously described function in , but in the absence of viral infection, deletion of the locus by CRISPR/Cas9 led to a reduction in brood size and a shortened lifespan.
View Article and Find Full Text PDFPLoS Biol
August 2025
Department of Biology and the Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
Spillover of viruses into novel host species occurs frequently. Often, spillover results in dead-end infections in novel hosts, sometimes, in stuttering transmission chains that die out, and rarely, in large epidemics with sustained transmission. If we could identify early which outcome will occur following a spillover event, we could more appropriately invest in efforts to surveil, respond to, or prevent disease emergence.
View Article and Find Full Text PDFNat Commun
August 2025
Institute of Integrative Systems Biology (I2SysBio), CSIC-Universitat de València, Paterna, València, Spain.
The C. elegans-Orsay virus pathosystem provides a powerful model for investigating the mechanisms that govern viral infection and immunity. Here, we focus on two key aspects of this interaction: the impact of lifelong latent infections and the dynamics of superinfection.
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