Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity

Detalhes bibliográficos
Autor(a) principal: Silva, Emiliana M.
Data de Publicação: 2019
Outros Autores: Conde, Jonas N., Allonso, Diego, Ventura, Gustavo T., Coelho, Diego R., Carneiro, Pedro Henrique, Silva, Manuela L., Paes, Marciano V., Rabelo, Kíssila, Weissmuller, Gilberto, Bisch, Paulo Mascarello, Mohana-Borges, Ronaldo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da FIOCRUZ (ARCA)
Texto Completo: https://www.arca.fiocruz.br/handle/icict/32914
Resumo: Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.
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spelling Silva, Emiliana M.Conde, Jonas N.Allonso, DiegoVentura, Gustavo T.Coelho, Diego R.Carneiro, Pedro HenriqueSilva, Manuela L.Paes, Marciano V.Rabelo, KíssilaWeissmuller, GilbertoBisch, Paulo MascarelloMohana-Borges, Ronaldo2019-05-02T15:49:17Z2019-05-02T15:49:17Z2019SILVA, Emiliana M. et al. Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde- 3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity. Scientific Reports, v. 9, n. 2651, 19p, 2019.2045-2322https://www.arca.fiocruz.br/handle/icict/3291410.1038/s41598-019-39157-7engNature ResearchVírus da DengueProteina NS3DENV2proteína GAPDHMecanismo molecularAlterações hepáticasDengue virusDENV2 NS3 proteinGAPDH proteinMolecular mechanismHepatic alterationsDengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activityinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleUniversidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Faculdade de Farmácia. Departamento de Biotecnologia Farmacêutica. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biodiversidade e Sustentabilidade. Macaé, RJ, Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório Interdisciplinar de Pesquisa Médica. Rio de Janeiro, RJ. Brasil.Universidade do Estado do Rio de Janeiro. Laboratório de Ultraestrutura e Biologia Tecidual. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Física Biológica. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Física Biológica. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.Dengue is an important mosquito-borne disease and a global public health problem. The disease is caused by dengue virus (DENV), which is a member of the Flaviviridae family and contains a positive single-stranded RNA genome that encodes a single precursor polyprotein that is further cleaved into structural and non-structural proteins. Among these proteins, the non-structural 3 (NS3) protein is very important because it forms a non-covalent complex with the NS2B cofactor, thereby forming the functional viral protease. NS3 also contains a C-terminal ATPase/helicase domain that is essential for RNA replication. Here, we identified 47 NS3-interacting partners using the yeast two-hybrid system. Among those partners, we highlight several proteins involved in host energy metabolism, such as apolipoprotein H, aldolase B, cytochrome C oxidase and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). GAPDH directly binds full-length NS3 and its isolated helicase and protease domains. Moreover, we observed an intense colocalization between the GAPDH and NS3 proteins in DENV2-infected Huh7.5.1 cells, in NS3-transfected BHK-21 cells and in hepatic tissue from a fatal dengue case. Taken together, these results suggest that the human GAPDH-DENV NS3 interaction is involved in hepatic metabolic alterations, which may contribute to the appearance of steatosis in dengue-infected patients. The interaction between GAPDH and full-length NS3 or its helicase domain in vitro as well as in NS3-transfected cells resulted in decreased GAPDH glycolytic activity. Reduced GAPDH glycolytic activity may lead to the accumulation of metabolic intermediates, shifting metabolism to alternative, non-glycolytic pathways. This report is the first to identify the interaction of the DENV2 NS3 protein with the GAPDH protein and to demonstrate that this interaction may play an important role in the molecular mechanism that triggers hepatic alterations.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; charset=utf-82991https://www.arca.fiocruz.br/bitstream/icict/32914/1/license.txt5a560609d32a3863062d77ff32785d58MD51ORIGINALMarciano_Paes_etal_IOC_2019.pdfMarciano_Paes_etal_IOC_2019.pdfapplication/pdf2757474https://www.arca.fiocruz.br/bitstream/icict/32914/2/Marciano_Paes_etal_IOC_2019.pdff484f68c0e57cb9176253927e0d15291MD52TEXTMarciano_Paes_etal_IOC_2019.pdf.txtMarciano_Paes_etal_IOC_2019.pdf.txtExtracted texttext/plain88853https://www.arca.fiocruz.br/bitstream/icict/32914/3/Marciano_Paes_etal_IOC_2019.pdf.txtda52980897820af932bec097c2737754MD53icict/329142019-05-03 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dc.title.pt_BR.fl_str_mv Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
title Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
spellingShingle Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
Silva, Emiliana M.
Vírus da Dengue
Proteina NS3
DENV2
proteína GAPDH
Mecanismo molecular
Alterações hepáticas
Dengue virus
DENV2 NS3 protein
GAPDH protein
Molecular mechanism
Hepatic alterations
title_short Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
title_full Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
title_fullStr Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
title_full_unstemmed Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
title_sort Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity
author Silva, Emiliana M.
author_facet Silva, Emiliana M.
Conde, Jonas N.
Allonso, Diego
Ventura, Gustavo T.
Coelho, Diego R.
Carneiro, Pedro Henrique
Silva, Manuela L.
Paes, Marciano V.
Rabelo, Kíssila
Weissmuller, Gilberto
Bisch, Paulo Mascarello
Mohana-Borges, Ronaldo
author_role author
author2 Conde, Jonas N.
Allonso, Diego
Ventura, Gustavo T.
Coelho, Diego R.
Carneiro, Pedro Henrique
Silva, Manuela L.
Paes, Marciano V.
Rabelo, Kíssila
Weissmuller, Gilberto
Bisch, Paulo Mascarello
Mohana-Borges, Ronaldo
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Silva, Emiliana M.
Conde, Jonas N.
Allonso, Diego
Ventura, Gustavo T.
Coelho, Diego R.
Carneiro, Pedro Henrique
Silva, Manuela L.
Paes, Marciano V.
Rabelo, Kíssila
Weissmuller, Gilberto
Bisch, Paulo Mascarello
Mohana-Borges, Ronaldo
dc.subject.other.pt_BR.fl_str_mv Vírus da Dengue
Proteina NS3
DENV2
proteína GAPDH
Mecanismo molecular
Alterações hepáticas
topic Vírus da Dengue
Proteina NS3
DENV2
proteína GAPDH
Mecanismo molecular
Alterações hepáticas
Dengue virus
DENV2 NS3 protein
GAPDH protein
Molecular mechanism
Hepatic alterations
dc.subject.en.pt_BR.fl_str_mv Dengue virus
DENV2 NS3 protein
GAPDH protein
Molecular mechanism
Hepatic alterations
description Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Laboratório de Genômica Estrutural. Rio de Janeiro, RJ, Brasil.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-05-02T15:49:17Z
dc.date.available.fl_str_mv 2019-05-02T15:49:17Z
dc.date.issued.fl_str_mv 2019
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 SILVA, Emiliana M. et al. Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde- 3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity. Scientific Reports, v. 9, n. 2651, 19p, 2019.
dc.identifier.uri.fl_str_mv https://www.arca.fiocruz.br/handle/icict/32914
dc.identifier.issn.pt_BR.fl_str_mv 2045-2322
dc.identifier.doi.none.fl_str_mv 10.1038/s41598-019-39157-7
identifier_str_mv SILVA, Emiliana M. et al. Dengue virus nonstructural 3 protein interacts directly with human glyceraldehyde- 3-phosphate dehydrogenase (GAPDH) and reduces its glycolytic activity. Scientific Reports, v. 9, n. 2651, 19p, 2019.
2045-2322
10.1038/s41598-019-39157-7
url https://www.arca.fiocruz.br/handle/icict/32914
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Nature Research
publisher.none.fl_str_mv Nature Research
dc.source.none.fl_str_mv reponame:Repositório Institucional da FIOCRUZ (ARCA)
instname:Fundação Oswaldo Cruz (FIOCRUZ)
instacron:FIOCRUZ
instname_str Fundação Oswaldo Cruz (FIOCRUZ)
instacron_str FIOCRUZ
institution FIOCRUZ
reponame_str Repositório Institucional da FIOCRUZ (ARCA)
collection Repositório Institucional da FIOCRUZ (ARCA)
bitstream.url.fl_str_mv https://www.arca.fiocruz.br/bitstream/icict/32914/1/license.txt
https://www.arca.fiocruz.br/bitstream/icict/32914/2/Marciano_Paes_etal_IOC_2019.pdf
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