TY - JOUR
T1 - An in vivo RNAi screening approach to identify host determinants of virus Replication
AU - Varble, Andrew
AU - Benitez, Asiel A.
AU - Schmid, Sonja
AU - Sachs, David
AU - Shim, Jaehee V.
AU - Rodriguez-Barrueco, Ruth
AU - Panis, Maryline
AU - Crumiller, Marshall
AU - Silva, Jose M.
AU - Sachidanandam, Ravi
AU - Tenoever, Benjamin R.
N1 - Funding Information:
This material is based upon work supported in part by the US Army Research Laboratory and the US Army Research Office under grant numbers W911NF-12-R-0012 and W911NF-08-1-0413. BtO is supported in part by the Burroughs Wellcome Fund. We also wish to thank Drs. B. Reizis (Columbia), R. Eisenman (Fred Hutchinson Cancer Research Center), D. Griffin (Johns Hopkins), A. Garcia-Sastre (MSSM), and P. Palese (MSSM) for the Zfx knockout fibroblasts, cDNA expression vector for Mga, SINV Capsid antibody, RIG-I antibody and Ddx58 knockout fibroblasts, and IAV antibody, respectively. Next-generation sequencing was performed by the Genomics Core Facility, Icahn Institute for Genomics and Multiscale Biology at Mount Sinai.
PY - 2013/9/11
Y1 - 2013/9/11
N2 - RNA interference (RNAi) has been extensively used to identify host factors affecting virus infection but requires exogenous delivery of short interfering RNAs (siRNAs), thus limiting the technique to nonphysiological infection models and a single defined cell type. We report an alternative screening approach using siRNA delivery via infection with a replication-competent RNA virus. In this system, natural selection, defined by siRNA production, permits the identification of host restriction factors through virus enrichment during a physiological infection. We validate this approach with a large-scale siRNA screen in the context of an in vivo alphavirus infection. Monitoring virus evolution across four independent screens identified two categories of enriched siRNAs: specific effectors of the direct antiviral arsenal and host factors that indirectly dampened the overall antiviral response. These results suggest that pathogenicity may be defined by the ability of the virus to antagonize broad cellular responses and specific antiviral factors.
AB - RNA interference (RNAi) has been extensively used to identify host factors affecting virus infection but requires exogenous delivery of short interfering RNAs (siRNAs), thus limiting the technique to nonphysiological infection models and a single defined cell type. We report an alternative screening approach using siRNA delivery via infection with a replication-competent RNA virus. In this system, natural selection, defined by siRNA production, permits the identification of host restriction factors through virus enrichment during a physiological infection. We validate this approach with a large-scale siRNA screen in the context of an in vivo alphavirus infection. Monitoring virus evolution across four independent screens identified two categories of enriched siRNAs: specific effectors of the direct antiviral arsenal and host factors that indirectly dampened the overall antiviral response. These results suggest that pathogenicity may be defined by the ability of the virus to antagonize broad cellular responses and specific antiviral factors.
UR - http://www.scopus.com/inward/record.url?scp=84883868163&partnerID=8YFLogxK
U2 - 10.1016/j.chom.2013.08.007
DO - 10.1016/j.chom.2013.08.007
M3 - Article
C2 - 24034620
AN - SCOPUS:84883868163
SN - 1931-3128
VL - 14
SP - 346
EP - 356
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 3
ER -