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


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.

SUBMITTER: Cheng KW 

PROVIDER: S-EPMC12696002 | biostudies-literature | 2025 Dec

REPOSITORIES: biostudies-literature

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

Cheng Karen W KW   Bhave Madhura M   Markhard Andrew L AL   Peng Duo D   Bhatt Karan D KD   Travisano Katherine A KA   Medicielo Josette V JV   Anaya Astrid A   Lembirik Sanae S   Njoya Leila L   Anantpadma Manu M   Kuhn Jens H JH   Puschnik Andreas S AS   Kistler Amy L AL  

Nature communications 20251210 1


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 add  ...[more]

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