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10.1016/j.celrep.2018.03.045

http://scihub22266oqcxt.onion/10.1016/j.celrep.2018.03.045
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C5939577!5939577!29642015
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suck abstract from ncbi


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pmid29642015      Cell+Rep 2018 ; 23 (2): 596-607
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  • Genome-wide CRISPR/Cas9 Screen Identifies Host Factors Essential for Influenza Virus Replication #MMPMID29642015
  • Han J; Perez JT; Chen C; Li Y; Benitez A; Kandasamy M; Lee Y; Andrade J; tenOever B; Manicassamy B
  • Cell Rep 2018[Apr]; 23 (2): 596-607 PMID29642015show ga
  • The emergence of influenza A viruses (IAVs) from zoonotic reservoirs poses a great threat to human health. As seasonal vaccines are ineffective against zoonotic strains, and newly transmitted viruses can quickly acquire drug resistance, there remains a need for host-directed therapeutics against IAVs. Here, we performed a genome-scale CRISPR/Cas9 knockout screen in human lung epithelial cells with a human isolate of an avian H5N1 strain. Several genes involved in sialic acid biosynthesis and related glycosylation pathways were highly enriched post-H5N1 selection, including SLC35A1, a sialic acid transporter essential for IAV receptor expression and thus viral entry. Importantly, we have identified capicua (CIC) as a negative regulator of cell-intrinsic immunity, as loss of CIC resulted in heightened antiviral responses and restricted replication of multiple viruses. Therefore, our study demonstrates that the CRISPR/Cas9 system can be utilized for the discovery of host factors critical for the replication of intracellular pathogens.
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