bioRxiv · 10.1101/2022.07.15.500120
Systematic functional interrogation of SARS-CoV-2 host factors using Perturb-seq
Abstract
Genomic and proteomic screens have identified numerous host factors of SARS-CoV-2, but efficient delineation of their molecular roles during infection remains a challenge. Here we use Perturb-seq, combining genetic perturbations with a single-cell readout, to investigate how inactivation of host factors changes the course of SARS-CoV-2 infection and the host response in human lung epithelial cells. Our high-dimensional data resolve complex phenotypes such as shifts in the stages of infection and modulations of the interferon response. However, only a small percentage of host factors showed such phenotypes upon perturbation. We further identified the NF-{kappa}B inhibitor I{kappa}B (NFKBIA), as well as the translation factors EIF4E2 and EIF4H as strong host dependency factors acting early in infection. Overall, our study provides massively parallel functional characterization of host factors of SARS-CoV-2 and quantitatively defines their roles both in virus-infected and bystander cells.
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Sunshine, S., Puschnik, A. S., Replogle, J. M., Laurie, M. T., Liu, J., Zha, B. S., Nunez, J. K., Byrum, J. R., McMorrow, A. H., Frieman, M. B., Winkler, J., Qiu, X., Rosenberg, O. S., Leonetti, M. D., Ye, C. J., Weissman, J. S., DeRisi, J. L., Hein, M. Y.. 2022-07-17. Systematic functional interrogation of SARS-CoV-2 host factors using Perturb-seq. https://doi.org/10.1101/2022.07.15.500120
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