CRISPR-Cas9 Screen for SARS-CoV-2 Host Dependency Factors
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Principal Investigator: Alex Compton Organization: DIVISION OF BASIC SCIENCES - NCI Fiscal Year: 2020 Award: $199,245 Funding agency: National Cancer Institute This project was initiated in spring of 2020 and is now in the preparatory phase. We have obtained CRISPR-Cas9 libraries from Juan Bonifacino that can be delivered to diverese cell types by lentiviral vectors. We have applied lentiviral vectors carrying CRISPR-Cas9 libraries to HeLa, Vero, and HEK293T-hACE2 cells and has selected cells with diverse gene inactivations using puromycin. These cells will be given to Rajini Mudhasani of USAMRIID for infection with wild-type SARS-CoV-2. Cells that are missing a crucial factor needed for infection will survive the otherwise cytopathic effects of productive SARS infection, resulting in the progressive enrichment of virus-resistant cells in culture over time. These cells will be subjected to bulk RNA sequencing in order to identify the guide RNA sequences associated with cell survival, thereby identifying the genes encoding host dependency factors. The initial results of the screen will be followed with targeted assays to confirm the functional role of a given gene during SARS-CoV-2 infection. We anticipate that infections of our genetically modified cell lines will begin in fall of 2020. Terms: <2019 novel coronavirus><2019-nCoV><Antiviral Therapy><Assay><Bioassay><Biologic Assays><Biological Assay><COVID-19 epidemic><COVID-19 pandemic><COVID19 epidemic><COVID19 pandemic><CRISPR editing screen><CRISPR library><CRISPR screen><CRISPR-based library><CRISPR-based screen><CRISPR/Cas9 library><CRISPR/Cas9 screen><Cell Body><Cell Line><Cell Survival><Cell Viability><CellLine><Cells><Clustered Regularly Interspaced Short Palindromic Repeats library><Collaborations><Communicable Diseases><Dependence><Development><Gene Inactivation><Gene Silencing><Genes><Genetic Screening><Guide RNA><HeLa><Hela Cells><Host Factor><Host Factor Protein><Human><Infection><Infectious Disease Pathway><Infectious Diseases><Infectious Disorder><Integration Host Factors><Lentiviral Vector><Lentivirus Vector><Medical Research><Modality><Modern Man><NIDDK><National Institute of Diabetes and Digestive and Kidney Diseases><Phase><Puromicina><Puromycin><Puromycine><Puromycinum><RNA Seq><RNA Sequences><RNA sequencing><RNAseq><Research Institute><Research Resources><Resistance><Resources><Role><SARS><SARS coronavirus disease><SARS-CoV disease><SARS-CoV-2><SARS-CoV2><SARS-associated coronavirus 2><SARS-coronavirus-2><SARS-related coronavirus 2><Screening Result><Severe Acute Respiratory Syndrome><Severe Acute Respiratory Syndrome CoV disease><Severe Acute Respiratory Syndrome coronavirus disease><Severe acute respiratory syndrome coronavirus 2><Strains Cell Lines><Time><Virus><Wuhan coronavirus><anti-viral therapy><cell type><clustered regularly interspaced short palindromic repeats screen><corona virus disease 2019 epidemic><corona virus disease 2019 pandemic><coronavirus disease 2019 epidemic><coronavirus disease 2019 pandemic><cultured cell line><developmental><falls><gRNA><genetically engineered cells><genetically modified cells><novel><resistant><response><social role><transcriptional silencing><transcriptome sequencing><viral infectious disease treatment>