A review of virus host factor discovery using CRISPR screening.

mBio

Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.

Published: November 2024

AI Article Synopsis

  • The development of genome-scale genetic screening methods like CRISPR knockout screens has significantly enhanced our understanding of how viruses interact with their hosts.
  • This review explores the impact of CRISPR screening on identifying novel host factors for various viruses, discussing its experimental design and key findings.
  • The authors also provide insights on customizing CRISPR methods for specific research questions and present examples, including flaviviruses and SARS-CoV-2, to illustrate the capabilities of these techniques in virus-host interaction studies.

Article Abstract

The emergence of genome-scale forward genetic screening techniques, such as Haploid Genetic screen and clustered regularly interspaced short palindromic repeats (CRISPR) knockout screen has opened new horizons in our understanding of virus infection biology. CRISPR screening has become a popular tool for the discovery of novel host factors for several viruses due to its specificity and efficiency in genome editing. Here, we review how CRISPR screening has revolutionized our understanding of virus-host interactions from scientific and technological viewpoints. A summary of the published screens conducted thus far to uncover virus host factors is presented, highlighting their experimental design and significant findings. We will outline relevant methods for customizing the CRISPR screening process to answer more specific hypotheses and compile a glossary of conducted CRISPR screens to show their design aspects. Furthermore, using flaviviruses and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as examples, we hope to offer a broad-based perspective on the capabilities of CRISPR screening to serve as a reference point to guide future unbiased discovery of virus host factors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11559068PMC
http://dx.doi.org/10.1128/mbio.03205-23DOI Listing

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