<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Yu DS</submitter><pubmed_abstract>Ebolavirus (EBOV) life cycle involves interactions with numerous host factors, but it remains poorly understood, as does pathogenesis. Herein, we synthesized 65 siRNAs targeting host genes mostly connected with aspects of the negative-sense RNA virus life cycle (including viral entry, uncoating, fusion, replication, assembly, and budding). We produced EBOV transcription- and replication-competent virus-like particles (trVLPs) to mimic the EBOV life cycle. After screening host factors associated with the trVLP life cycle, we assessed interactions of host proteins with trVLP glycoprotein (GP), VP40, and RNA by co-immunoprecipitation (Co-IP) and chromatin immunoprecipitation (ChIP). The results demonstrate that RNAi silencing with 11 siRNAs (ANXA5, ARFGAP1, FLT4, GRP78, HSPA1A, HSP90AB1, HSPA</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>2724</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6240689</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chaperones, Membrane Trafficking and Signal Transduction Proteins Regulate Zaire Ebola Virus trVLPs and Interact With trVLP Elements.</pubmed_title><pmcid>PMC6240689</pmcid><pubmed_authors>Wu ZG</pubmed_authors><pubmed_authors>Hu CY</pubmed_authors><pubmed_authors>Yu DS</pubmed_authors><pubmed_authors>Weng TH</pubmed_authors><pubmed_authors>Yao HP</pubmed_authors><pubmed_authors>Wu NP</pubmed_authors><pubmed_authors>Cheng LF</pubmed_authors><pubmed_authors>Li YH</pubmed_authors><pubmed_authors>Li LJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chaperones, Membrane Trafficking and Signal Transduction Proteins Regulate Zaire Ebola Virus trVLPs and Interact With trVLP Elements.</name><description>Ebolavirus (EBOV) life cycle involves interactions with numerous host factors, but it remains poorly understood, as does pathogenesis. Herein, we synthesized 65 siRNAs targeting host genes mostly connected with aspects of the negative-sense RNA virus life cycle (including viral entry, uncoating, fusion, replication, assembly, and budding). We produced EBOV transcription- and replication-competent virus-like particles (trVLPs) to mimic the EBOV life cycle. After screening host factors associated with the trVLP life cycle, we assessed interactions of host proteins with trVLP glycoprotein (GP), VP40, and RNA by co-immunoprecipitation (Co-IP) and chromatin immunoprecipitation (ChIP). The results demonstrate that RNAi silencing with 11 siRNAs (ANXA5, ARFGAP1, FLT4, GRP78, HSPA1A, HSP90AB1, HSPA</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2026-04-08T05:10:01.61Z</modification><creation>2019-03-27T00:09:46Z</creation></dates><accession>S-EPMC6240689</accession><cross_references><pubmed>30483236</pubmed><doi>10.3389/fmicb.2018.02724</doi></cross_references></HashMap>