Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da FIOCRUZ (ARCA) |
Texto Completo: | https://www.arca.fiocruz.br/handle/icict/59574 |
Resumo: | Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Bioquímica Médica Leopoldo de Meis. Rio de Janeiro, RJ, Brasil / Universidade Federal Rio do Janeiro. Centro de Ciências da Saúde. Escola de Educação Física e Desportos. Departamento de Biociências da Atividade Física. Rio de Janeiro, RJ, Brasil / Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem. Rio de Janeiro, RJ, Brasil. |
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Real-Hohn, AntonioProvance, D. WilliamGonçalves, Rafael BragaDenani, Caio BidueiraOliveira, Andrea Cheble deSalerno, Verônica P.Gomes, Andre Marco Oliveira2023-07-13T19:29:35Z2023-07-13T19:29:35Z2017REAL-HOHN, Antonio et al. Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication. Scientific Reports, v. 7, n. 1, p. 1-15, Dec. 2017.2045-2322https://www.arca.fiocruz.br/handle/icict/5957410.1038/S41598-017-17501-Z2045-2322engNature Publishing GroupActin CytoskeletonEnterovirus InfectionsHeLa CellsHumansMethylmalonic AcidMyosin Heavy ChainsMyosin Type VMyosin-Light-Chain KinasePhosphorylationRhinovirusVirus InternalizationVirus ReplicationRecycling endosomesHela-cellsIn-vivoRNAVirusEntryEndocytosisExpressionInfectionMultipleImpairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replicationinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleUniversidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Bioquímica Médica Leopoldo de Meis. Rio de Janeiro, RJ, Brasil / Universidade Federal Rio do Janeiro. Centro de Ciências da Saúde. Escola de Educação Física e Desportos. Departamento de Biociências da Atividade Física. Rio de Janeiro, RJ, Brasil / Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Centro de Desenvolvimento Tecnológico em Saúde. Instituto Nacional de Ciência e Tecnologia de Inovação em Doenças de Populações Negligenciadas. Rio de Janeiro, RJ, Brasil.Universidade Federal do Estado do Rio de Janeiro. Instituto Biomédico. Departamento de Bioquímica. Rio de Janeiro, RJ, Brasil / Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Bioquímica Médica Leopoldo de Meis. Rio de Janeiro, RJ, Brasil / Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Bioquímica Médica Leopoldo de Meis. Rio de Janeiro, RJ, Brazil / Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem. Rio de Janeiro, RJ, Brasil.Universidade Federal Rio do Janeiro. Centro de Ciências da Saúde. Escola de Educação Física e Desportos. Departamento de Biociências da Atividade Física. Rio de Janeiro, RJ, BrasilUniversidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Bioquímica Médica Leopoldo de Meis. Rio de Janeiro, RJ, Brazil / Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Centro de Desenvolvimento Tecnológico em Saúde. Rio de Janeiro, RJ, Brasil.Together, the three human rhinovirus (RV) species are the most frequent cause of the common cold. Because of their high similarity with other viral species of the genus Enterovirus, within the large family Picornaviridae, studies on RV infectious activities often offer a less pathogenic model for more aggressive enteroviruses, e.g. poliovirus or EV71. Picornaviruses enter via receptor mediated endocytosis and replicate in the cytosol. Most of them depend on functional F-actin, Rab proteins, and probably motor proteins. To assess the latter, we evaluated the role of myosin light chain kinase (MLCK) and two myosin V isoforms (Va and Vb) in RV-B14 infection. We report that ML-9, a very specific MLCK inhibitor, dramatically reduced RV-B14 entry. We also demonstrate that RV-B14 infection in cells expressing dominant-negative forms of myosin Va and Vb was impaired after virus entry. Using immunofluorescent localization and immunoprecipitation, we show that myosin Va co-localized with RV-B14 exclusively after viral entry (15 min post infection) and that myosin Vb was present in the clusters of newly synthesized RNA in infected cells. These clusters, observed at 180 min post infection, are reminiscent of replication sites. Taken together, these results identify myosin light chain kinase, myosin Va and myosin Vb as new players in RV-B14 infection that participate directly or indirectly in different stages of the viral cycle.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txttext/plain1748https://www.arca.fiocruz.br/bitstream/icict/59574/1/license.txt8a4605be74aa9ea9d79846c1fba20a33MD51ORIGINAL10.1038_s41598-017-17501-z.pdfapplication/pdf3957442https://www.arca.fiocruz.br/bitstream/icict/59574/2/10.1038_s41598-017-17501-z.pdfb228c4166a8b440a90ea47f1bafe222dMD52icict/595742023-07-20 15:06:18.206oai:www.arca.fiocruz.br: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Repositório InstitucionalPUBhttps://www.arca.fiocruz.br/oai/requestrepositorio.arca@fiocruz.bropendoar:21352023-07-20T18:06:18Repositório Institucional da FIOCRUZ (ARCA) - Fundação Oswaldo Cruz (FIOCRUZ)false |
dc.title.en_US.fl_str_mv |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication |
title |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication |
spellingShingle |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication Real-Hohn, Antonio Actin Cytoskeleton Enterovirus Infections HeLa Cells Humans Methylmalonic Acid Myosin Heavy Chains Myosin Type V Myosin-Light-Chain Kinase Phosphorylation Rhinovirus Virus Internalization Virus Replication Recycling endosomes Hela-cells In-vivo RNA Virus Entry Endocytosis Expression Infection Multiple |
title_short |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication |
title_full |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication |
title_fullStr |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication |
title_full_unstemmed |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication |
title_sort |
Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication |
author |
Real-Hohn, Antonio |
author_facet |
Real-Hohn, Antonio Provance, D. William Gonçalves, Rafael Braga Denani, Caio Bidueira Oliveira, Andrea Cheble de Salerno, Verônica P. Gomes, Andre Marco Oliveira |
author_role |
author |
author2 |
Provance, D. William Gonçalves, Rafael Braga Denani, Caio Bidueira Oliveira, Andrea Cheble de Salerno, Verônica P. Gomes, Andre Marco Oliveira |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Real-Hohn, Antonio Provance, D. William Gonçalves, Rafael Braga Denani, Caio Bidueira Oliveira, Andrea Cheble de Salerno, Verônica P. Gomes, Andre Marco Oliveira |
dc.subject.mesh.en_US.fl_str_mv |
Actin Cytoskeleton Enterovirus Infections HeLa Cells Humans Methylmalonic Acid Myosin Heavy Chains Myosin Type V Myosin-Light-Chain Kinase Phosphorylation Rhinovirus Virus Internalization Virus Replication |
topic |
Actin Cytoskeleton Enterovirus Infections HeLa Cells Humans Methylmalonic Acid Myosin Heavy Chains Myosin Type V Myosin-Light-Chain Kinase Phosphorylation Rhinovirus Virus Internalization Virus Replication Recycling endosomes Hela-cells In-vivo RNA Virus Entry Endocytosis Expression Infection Multiple |
dc.subject.en.en_US.fl_str_mv |
Recycling endosomes Hela-cells In-vivo RNA Virus Entry Endocytosis Expression Infection Multiple |
description |
Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Bioquímica Médica Leopoldo de Meis. Rio de Janeiro, RJ, Brasil / Universidade Federal Rio do Janeiro. Centro de Ciências da Saúde. Escola de Educação Física e Desportos. Departamento de Biociências da Atividade Física. Rio de Janeiro, RJ, Brasil / Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem. Rio de Janeiro, RJ, Brasil. |
publishDate |
2017 |
dc.date.issued.fl_str_mv |
2017 |
dc.date.accessioned.fl_str_mv |
2023-07-13T19:29:35Z |
dc.date.available.fl_str_mv |
2023-07-13T19:29:35Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
REAL-HOHN, Antonio et al. Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication. Scientific Reports, v. 7, n. 1, p. 1-15, Dec. 2017. |
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https://www.arca.fiocruz.br/handle/icict/59574 |
dc.identifier.issn.en_US.fl_str_mv |
2045-2322 |
dc.identifier.doi.none.fl_str_mv |
10.1038/S41598-017-17501-Z |
dc.identifier.eissn.none.fl_str_mv |
2045-2322 |
identifier_str_mv |
REAL-HOHN, Antonio et al. Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication. Scientific Reports, v. 7, n. 1, p. 1-15, Dec. 2017. 2045-2322 10.1038/S41598-017-17501-Z |
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https://www.arca.fiocruz.br/handle/icict/59574 |
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Nature Publishing Group |
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Nature Publishing Group |
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