Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1007/s00705-018-3911-x http://hdl.handle.net/11449/176394 |
Resumo: | Zika virus (ZIKV) is a flavivirus that has been highly correlated with the development of neurological disorders and other malformations in newborns and stillborn fetuses after congenital infection. This association is supported by the presence of ZIKV in the fetal brain and amniotic fluid, and findings suggest that infection of the placental barrier is a critical step for fetal ZIKV infection in utero. Therefore, relevant models to investigate the interaction between ZIKV and placental tissues are essential for understanding the pathogenesis of Zika syndrome. In this report, we demonstrate that explant tissue from full-term human placentas sustains a productive ZIKV infection, though the results depend on the strain. Viral infection was found to be associated with pro-inflammatory cytokine expression and apoptosis of the infected tissue, and these findings confirm that placental explants are targets of ZIKV replication. We propose that human placental explants are useful as a model for studying ZIKV infection ex vivo. |
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Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosisZika virus (ZIKV) is a flavivirus that has been highly correlated with the development of neurological disorders and other malformations in newborns and stillborn fetuses after congenital infection. This association is supported by the presence of ZIKV in the fetal brain and amniotic fluid, and findings suggest that infection of the placental barrier is a critical step for fetal ZIKV infection in utero. Therefore, relevant models to investigate the interaction between ZIKV and placental tissues are essential for understanding the pathogenesis of Zika syndrome. In this report, we demonstrate that explant tissue from full-term human placentas sustains a productive ZIKV infection, though the results depend on the strain. Viral infection was found to be associated with pro-inflammatory cytokine expression and apoptosis of the infected tissue, and these findings confirm that placental explants are targets of ZIKV replication. We propose that human placental explants are useful as a model for studying ZIKV infection ex vivo.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Biology School of Biosciences Humanities and the Exact Sciences São Paulo State University (UNESP), São José do Rio PretoFederal University of São Paulo (UNIFESP)Brazilian Biosciences National Laboratory (LNBio) National Center for Research in Energy and Materials (CNPEM)Paulo de Góes Department of Microbiology Federal University of Rio de Janeiro (UFRJ)George Mason UniversityVirology Research Laboratory Department of Dermatological Infectious and Parasitic Diseases São José do Rio Preto School of Medicine (FAMERP), São José do Rio PretoDepartment of Biology School of Biosciences Humanities and the Exact Sciences São Paulo State University (UNESP), São José do Rio PretoFAPESP: 2013/21719-3Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)National Center for Research in Energy and Materials (CNPEM)Universidade Federal do Rio de Janeiro (UFRJ)George Mason UniversitySão José do Rio Preto School of Medicine (FAMERP)Ribeiro, Milene Rocha [UNESP]Moreli, Jusciele BroginMarques, Rafael EliasPapa, Michelle PremazziMeuren, Lana MonteiroRahal, Paula [UNESP]de Arruda, Luciana BarrosOliani, Antonio HelioOliani, Denise Cristina Mós VazOliani, Sonia Maria [UNESP]Narayanan, AarthiNogueira, Maurício Lacerda2018-12-11T17:20:38Z2018-12-11T17:20:38Z2018-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2687-2699application/pdfhttp://dx.doi.org/10.1007/s00705-018-3911-xArchives of Virology, v. 163, n. 10, p. 2687-2699, 2018.0304-8608http://hdl.handle.net/11449/17639410.1007/s00705-018-3911-x2-s2.0-850480452282-s2.0-85048045228.pdf79910823626712120000-0001-5693-6148Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengArchives of Virology0,973info:eu-repo/semantics/openAccess2023-10-14T06:10:05Zoai:repositorio.unesp.br:11449/176394Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:55:53.532120Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis |
title |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis |
spellingShingle |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis Ribeiro, Milene Rocha [UNESP] |
title_short |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis |
title_full |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis |
title_fullStr |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis |
title_full_unstemmed |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis |
title_sort |
Zika-virus-infected human full-term placental explants display pro-inflammatory responses and undergo apoptosis |
author |
Ribeiro, Milene Rocha [UNESP] |
author_facet |
Ribeiro, Milene Rocha [UNESP] Moreli, Jusciele Brogin Marques, Rafael Elias Papa, Michelle Premazzi Meuren, Lana Monteiro Rahal, Paula [UNESP] de Arruda, Luciana Barros Oliani, Antonio Helio Oliani, Denise Cristina Mós Vaz Oliani, Sonia Maria [UNESP] Narayanan, Aarthi Nogueira, Maurício Lacerda |
author_role |
author |
author2 |
Moreli, Jusciele Brogin Marques, Rafael Elias Papa, Michelle Premazzi Meuren, Lana Monteiro Rahal, Paula [UNESP] de Arruda, Luciana Barros Oliani, Antonio Helio Oliani, Denise Cristina Mós Vaz Oliani, Sonia Maria [UNESP] Narayanan, Aarthi Nogueira, Maurício Lacerda |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) National Center for Research in Energy and Materials (CNPEM) Universidade Federal do Rio de Janeiro (UFRJ) George Mason University São José do Rio Preto School of Medicine (FAMERP) |
dc.contributor.author.fl_str_mv |
Ribeiro, Milene Rocha [UNESP] Moreli, Jusciele Brogin Marques, Rafael Elias Papa, Michelle Premazzi Meuren, Lana Monteiro Rahal, Paula [UNESP] de Arruda, Luciana Barros Oliani, Antonio Helio Oliani, Denise Cristina Mós Vaz Oliani, Sonia Maria [UNESP] Narayanan, Aarthi Nogueira, Maurício Lacerda |
description |
Zika virus (ZIKV) is a flavivirus that has been highly correlated with the development of neurological disorders and other malformations in newborns and stillborn fetuses after congenital infection. This association is supported by the presence of ZIKV in the fetal brain and amniotic fluid, and findings suggest that infection of the placental barrier is a critical step for fetal ZIKV infection in utero. Therefore, relevant models to investigate the interaction between ZIKV and placental tissues are essential for understanding the pathogenesis of Zika syndrome. In this report, we demonstrate that explant tissue from full-term human placentas sustains a productive ZIKV infection, though the results depend on the strain. Viral infection was found to be associated with pro-inflammatory cytokine expression and apoptosis of the infected tissue, and these findings confirm that placental explants are targets of ZIKV replication. We propose that human placental explants are useful as a model for studying ZIKV infection ex vivo. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:20:38Z 2018-12-11T17:20:38Z 2018-10-01 |
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.uri.fl_str_mv |
http://dx.doi.org/10.1007/s00705-018-3911-x Archives of Virology, v. 163, n. 10, p. 2687-2699, 2018. 0304-8608 http://hdl.handle.net/11449/176394 10.1007/s00705-018-3911-x 2-s2.0-85048045228 2-s2.0-85048045228.pdf 7991082362671212 0000-0001-5693-6148 |
url |
http://dx.doi.org/10.1007/s00705-018-3911-x http://hdl.handle.net/11449/176394 |
identifier_str_mv |
Archives of Virology, v. 163, n. 10, p. 2687-2699, 2018. 0304-8608 10.1007/s00705-018-3911-x 2-s2.0-85048045228 2-s2.0-85048045228.pdf 7991082362671212 0000-0001-5693-6148 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Archives of Virology 0,973 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
2687-2699 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1808128437111488512 |