<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(11)</volume><submitter>Popova TG</submitter><pubmed_abstract>Rift valley fever virus (RVFV) infection is an emerging zoonotic disease endemic in many countries of sub-Saharan Africa and in Egypt. In this study we show that human small airway epithelial cells are highly susceptible to RVFV virulent strain ZH-501 and the attenuated strain MP-12. We used the reverse-phase protein arrays technology to identify phosphoprotein signaling pathways modulated during infection of cultured airway epithelium. ZH-501 infection induced activation of MAP kinases (p38, JNK and ERK) and downstream transcriptional factors [STAT1 (Y701), ATF2 (T69/71), MSK1 (S360) and CREB (S133)]. NF-κB phosphorylation was also increased. Activation of p53 (S15, S46) correlated with the increased levels of cleaved effector caspase-3, -6 and -7, indicating activation of the extrinsic a</pubmed_abstract><journal>PloS one</journal><pagination>e13805</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2972203</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Reverse-phase phosphoproteome analysis of signaling pathways induced by Rift valley fever virus in human small airway epithelial cells.</pubmed_title><pmcid>PMC2972203</pmcid><pubmed_authors>Liotta L</pubmed_authors><pubmed_authors>Bailey C</pubmed_authors><pubmed_authors>Narayanan A</pubmed_authors><pubmed_authors>Kashanchi F</pubmed_authors><pubmed_authors>Kehn-Hall K</pubmed_authors><pubmed_authors>Espina V</pubmed_authors><pubmed_authors>Turell MJ</pubmed_authors><pubmed_authors>Kidd J</pubmed_authors><pubmed_authors>Petricoin EF</pubmed_authors><pubmed_authors>Popova TG</pubmed_authors><pubmed_authors>Popov SG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reverse-phase phosphoproteome analysis of signaling pathways induced by Rift valley fever virus in human small airway epithelial cells.</name><description>Rift valley fever virus (RVFV) infection is an emerging zoonotic disease endemic in many countries of sub-Saharan Africa and in Egypt. In this study we show that human small airway epithelial cells are highly susceptible to RVFV virulent strain ZH-501 and the attenuated strain MP-12. We used the reverse-phase protein arrays technology to identify phosphoprotein signaling pathways modulated during infection of cultured airway epithelium. ZH-501 infection induced activation of MAP kinases (p38, JNK and ERK) and downstream transcriptional factors [STAT1 (Y701), ATF2 (T69/71), MSK1 (S360) and CREB (S133)]. NF-κB phosphorylation was also increased. Activation of p53 (S15, S46) correlated with the increased levels of cleaved effector caspase-3, -6 and -7, indicating activation of the extrinsic a</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Nov</publication><modification>2025-04-04T21:04:39.141Z</modification><creation>2019-03-26T23:09:05Z</creation></dates><accession>S-EPMC2972203</accession><cross_references><pubmed>21072193</pubmed><doi>10.1371/journal.pone.0013805</doi></cross_references></HashMap>