TY - JOUR
T1 - RNAi screening reveals requirement for host cell secretory pathway in infection by diverse families of negative-strand RNA viruses
AU - Panda, Debasis
AU - Das, Anshuman
AU - Dinh, Phat X.
AU - Subramaniam, Sakthivel
AU - Nayak, Debasis
AU - Barrows, Nicholas J.
AU - Pearson, James L.
AU - Thompson, Jesse
AU - Kelly, David L.
AU - Ladunga, Istvan
AU - Pattnaik, Asit K.
PY - 2011/11/22
Y1 - 2011/11/22
N2 - Negative-strand (NS) RNA viruses comprise many pathogens that cause serious diseases in humans and animals. Despite their clinical importance, little is known about the host factors required for their infection. Using vesicular stomatitis virus (VSV), a prototypic NS RNA virus in the family Rhabdoviridae, we conducted a human genomewide siRNA screen and identified 72 host genes required for viral infection. Many of these identified genes were also required for infection by two other NS RNA viruses, the lymphocytic choriomeningitis virus of the Arenaviridae family and human parainfluenza virus type 3 of the Paramyxoviridae family. Genes affecting different stages of VSV infection, such as entry/uncoating, gene expression, and assembly/release,were identified.Depletion of the proteins of the coatomer complex I or its upstream effectors ARF1 or GBF1 led to detection of reduced levels of VSV RNA. Coatomer complex I was also required for infection of lymphocytic choriomeningitis virus and human parainfluenza virus type 3. These results highlight the evolutionarily conserved requirements for gene expression of diverse families of NS RNA viruses and demonstrate the involvement of host cell secretory pathway in the process.
AB - Negative-strand (NS) RNA viruses comprise many pathogens that cause serious diseases in humans and animals. Despite their clinical importance, little is known about the host factors required for their infection. Using vesicular stomatitis virus (VSV), a prototypic NS RNA virus in the family Rhabdoviridae, we conducted a human genomewide siRNA screen and identified 72 host genes required for viral infection. Many of these identified genes were also required for infection by two other NS RNA viruses, the lymphocytic choriomeningitis virus of the Arenaviridae family and human parainfluenza virus type 3 of the Paramyxoviridae family. Genes affecting different stages of VSV infection, such as entry/uncoating, gene expression, and assembly/release,were identified.Depletion of the proteins of the coatomer complex I or its upstream effectors ARF1 or GBF1 led to detection of reduced levels of VSV RNA. Coatomer complex I was also required for infection of lymphocytic choriomeningitis virus and human parainfluenza virus type 3. These results highlight the evolutionarily conserved requirements for gene expression of diverse families of NS RNA viruses and demonstrate the involvement of host cell secretory pathway in the process.
KW - Host cell factors for virus infection
KW - RNA interference
KW - Transcription and replication
UR - http://www.scopus.com/inward/record.url?scp=82755168802&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=82755168802&partnerID=8YFLogxK
U2 - 10.1073/pnas.1113643108
DO - 10.1073/pnas.1113643108
M3 - Article
C2 - 22065774
AN - SCOPUS:82755168802
SN - 0027-8424
VL - 108
SP - 19036
EP - 19041
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 47
ER -