<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(3)</volume><submitter>Deffrasnes C</submitter><pubmed_abstract>Hendra and Nipah viruses (genus Henipavirus, family Paramyxoviridae) are highly pathogenic bat-borne viruses. The need for high biocontainment when studying henipaviruses has hindered the development of therapeutics and knowledge of the viral infection cycle. We have performed a genome-wide siRNA screen at biosafety level 4 that identified 585 human proteins required for henipavirus infection. The host protein with the largest impact was fibrillarin, a nucleolar methyltransferase that was also required by measles, mumps and respiratory syncytial viruses for infection. While not required for cell entry, henipavirus RNA and protein syntheses were greatly impaired in cells lacking fibrillarin, indicating a crucial role in the RNA replication phase of infection. During infection, the Hendra vi</pubmed_abstract><journal>PLoS pathogens</journal><pagination>e1005478</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4806981</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-wide siRNA Screening at Biosafety Level 4 Reveals a Crucial Role for Fibrillarin in Henipavirus Infection.</pubmed_title><pmcid>PMC4806981</pmcid><pubmed_authors>Simpson KJ</pubmed_authors><pubmed_authors>Marsh GA</pubmed_authors><pubmed_authors>Bean AG</pubmed_authors><pubmed_authors>Gould CM</pubmed_authors><pubmed_authors>Tompkins SM</pubmed_authors><pubmed_authors>Rootes CL</pubmed_authors><pubmed_authors>Lowenthal JW</pubmed_authors><pubmed_authors>Stewart CR</pubmed_authors><pubmed_authors>Deffrasnes C</pubmed_authors><pubmed_authors>Wang LF</pubmed_authors><pubmed_authors>Grusovin J</pubmed_authors><pubmed_authors>Monaghan P</pubmed_authors><pubmed_authors>Lo MK</pubmed_authors><pubmed_authors>Adams TE</pubmed_authors><pubmed_authors>Foo CH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide siRNA Screening at Biosafety Level 4 Reveals a Crucial Role for Fibrillarin in Henipavirus Infection.</name><description>Hendra and Nipah viruses (genus Henipavirus, family Paramyxoviridae) are highly pathogenic bat-borne viruses. The need for high biocontainment when studying henipaviruses has hindered the development of therapeutics and knowledge of the viral infection cycle. We have performed a genome-wide siRNA screen at biosafety level 4 that identified 585 human proteins required for henipavirus infection. The host protein with the largest impact was fibrillarin, a nucleolar methyltransferase that was also required by measles, mumps and respiratory syncytial viruses for infection. While not required for cell entry, henipavirus RNA and protein syntheses were greatly impaired in cells lacking fibrillarin, indicating a crucial role in the RNA replication phase of infection. During infection, the Hendra vi</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2025-04-04T20:13:17.192Z</modification><creation>2019-03-26T22:47:03Z</creation></dates><accession>S-EPMC4806981</accession><cross_references><pubmed>27010548</pubmed><doi>10.1371/journal.ppat.1005478</doi></cross_references></HashMap>