Replicon-based genome-wide CRISPR knockout screening for the identification of host factors involved in viral replication

Nat Commun. 2025 Dec 10;16(1):11028. doi: 10.1038/s41467-025-65979-3.

Abstract

We describe a viral replicon-based CRISPR knockout (KO) screening approach to specifically identify host factors essential for viral replication which are often missed in live virus screens. We benchmark the replicon screening using a stable fluorescent dengue virus type 2 (DENV-2) replicon cell line and successfully identify host genes known to be required for viral DENV-2 replication (e.g., endoplasmic reticulum membrane complex and oligosaccharyltransferase complex components), along with additional genes that have not been reported in prior CRISPR KO screens with DENV-2. We extend this replicon screening approach to chikungunya virus (CHIKV), a positive-sense RNA virus, and Ebola virus (EBOV), a negative-sense RNA virus, and identify distinct sets of genes required for replication of each virus. Our findings indicate that viral replicon-based CRISPR screens are a useful approach to identify host factors essential for replication of diverse viruses and to elucidate potential novel targets for host-directed medical countermeasures.

MeSH terms

  • Animals
  • CRISPR-Cas Systems*
  • Cell Line
  • Chikungunya virus / genetics
  • Chikungunya virus / physiology
  • Clustered Regularly Interspaced Short Palindromic Repeats
  • Dengue Virus* / genetics
  • Dengue Virus* / physiology
  • Ebolavirus / genetics
  • Ebolavirus / physiology
  • Gene Knockout Techniques / methods
  • HEK293 Cells
  • Hexosyltransferases / genetics
  • Hexosyltransferases / metabolism
  • Host-Pathogen Interactions* / genetics
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Replicon* / genetics
  • Virus Replication* / genetics

Substances

  • Membrane Proteins
  • Hexosyltransferases