Genetic determinants of COVID-19 drug efficacy revealed by genome-wide CRISPR screens
Jiang, W.; Yang, A.; Ma, J.; Lv, D.; Liu, M.; Xu, L.; Wang, C.; He, Z.; Chen, S.; Zhao, J.; Chen, S.; Jiang, Q.; Chu, Y.; Shan, L.; Zhou, Z.; Zhao, Y.; Long, G.; Jiang, H.
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Immunomodulatory agents dexamethasone and colchicine, antiviral drugs remdesivir, favipiravir and ribavirin, as well as antimalarial drugs chloroquine phosphate and hydroxychloroquine are currently used in the combat against COVID-191-16. However, whether some of these drugs have clinical efficacy for COVID-19 is under debate. Moreover, these drugs are applied in COVID-19 patients with little knowledge of genetic biomarkers, which will hurt patient outcome. To answer these questions, we designed a screen approach that could employ genome-wide sgRNA libraries to systematically uncover genes crucial for these drugs action. Here we present our findings, including genes crucial for the import, export, metabolic activation and inactivation of remdesivir, as well as genes that regulate colchicine and dexamethasones immunosuppressive effects. Our findings provide preliminary information for developing urgently needed genetic biomarkers for these drugs. Such biomarkers will help better interpret COVID-19 clinical trial data and point to how to stratify COVID-19 patients for proper treatment with these drugs.
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