<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang LK</submitter><funding>National key R&amp;amp;D Program of China</funding><funding>National Natural Science Foundation of China</funding><funding>Youth Innovation Promotion Association of the Chinese Academy of Sciences</funding><pagination>e00308-19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6498065</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>93(10)</volume><pubmed_abstract>Severe fever with thrombocytopenia syndrome (SFTS) is an emerging, highly pathogenic, infectious disease caused by infection with a newly discovered tick-borne phlebovirus, SFTS virus (SFTSV). Limited information on the molecular mechanism of SFTSV infection and pathogenesis impedes the development of effective vaccines and drugs for SFTS prevention and treatment. In this study, an isobaric tag for relative and absolute quantification (iTRAQ)-based quantitative proteomic analysis of SFTSV-infected HEK 293 cells was performed to explore dynamic host cellular protein responses toward SFTSV infection. A total of 433 of 5,606 host proteins involved in different biological processes were differentially regulated by SFTSV infection. The proteomic results highlighted a potential role of endoplasm</pubmed_abstract><journal>Journal of virology</journal><pubmed_title>Quantitative Proteomic Analysis Reveals Unfolded-Protein Response Involved in Severe Fever with Thrombocytopenia Syndrome Virus Infection.</pubmed_title><pmcid>PMC6498065</pmcid><funding_grant_id>2013219</funding_grant_id><funding_grant_id>2018367</funding_grant_id><funding_grant_id>2016YFC1200400</funding_grant_id><funding_grant_id>31621061</funding_grant_id><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Zhang LK</pubmed_authors><pubmed_authors>Xin Q</pubmed_authors><pubmed_authors>Xiao G</pubmed_authors><pubmed_authors>Shen S</pubmed_authors><pubmed_authors>Shang W</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Deng F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantitative Proteomic Analysis Reveals Unfolded-Protein Response Involved in Severe Fever with Thrombocytopenia Syndrome Virus Infection.</name><description>Severe fever with thrombocytopenia syndrome (SFTS) is an emerging, highly pathogenic, infectious disease caused by infection with a newly discovered tick-borne phlebovirus, SFTS virus (SFTSV). Limited information on the molecular mechanism of SFTSV infection and pathogenesis impedes the development of effective vaccines and drugs for SFTS prevention and treatment. In this study, an isobaric tag for relative and absolute quantification (iTRAQ)-based quantitative proteomic analysis of SFTSV-infected HEK 293 cells was performed to explore dynamic host cellular protein responses toward SFTSV infection. A total of 433 of 5,606 host proteins involved in different biological processes were differentially regulated by SFTSV infection. The proteomic results highlighted a potential role of endoplasm</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 May</publication><modification>2025-04-19T11:04:37.05Z</modification><creation>2019-07-01T13:45:48Z</creation></dates><accession>S-EPMC6498065</accession><cross_references><pubmed>30842332</pubmed><doi>10.1128/JVI.00308-19</doi></cross_references></HashMap>