| Literature DB >> 35732867 |
Juliana Minardi Nascimento1,2,3, Danielle Gouvêa-Junqueira1, Giuliana S Zuccoli1, Carolina da Silva Gouveia Pedrosa2, Caroline Brandão-Teles1, Fernanda Crunfli1, André S L M Antunes1, Juliana S Cassoli1,4, Karina Karmirian2, José Alexandre Salerno2, Gabriela Fabiano de Souza5, Stéfanie Primon Muraro5, Jose Luiz Proenca-Módena5, Luiza M Higa6, Amilcar Tanuri6, Patricia P Garcez2,7, Stevens K Rehen8,9, Daniel Martins-de-Souza10,11,12,13.
Abstract
Brain abnormalities and congenital malformations have been linked to the circulating strain of Zika virus (ZIKV) in Brazil since 2016 during the microcephaly outbreak; however, the molecular mechanisms behind several of these alterations and differential viral molecular targets have not been fully elucidated. Here we explore the proteomic alterations induced by ZIKV by comparing the Brazilian (Br ZIKV) and the African (MR766) viral strains, in addition to comparing them to the molecular responses to the Dengue virus type 2 (DENV). Neural stem cells (NSCs) derived from induced pluripotent stem (iPSCs) were cultured both as monolayers and in suspension (resulting in neurospheres), which were then infected with ZIKV (Br ZIKV or ZIKV MR766) or DENV to assess alterations within neural cells. Large-scale proteomic analyses allowed the comparison not only between viral strains but also regarding the two- and three-dimensional cellular models of neural cells derived from iPSCs, and the effects on their interaction. Altered pathways and biological processes were observed related to cell death, cell cycle dysregulation, and neurogenesis. These results reinforce already published data and provide further information regarding the biological alterations induced by ZIKV and DENV in neural cells.Entities:
Keywords: Flaviviridae; Microcephaly; Neural cells; Neurodevelopment; iPS
Mesh:
Year: 2022 PMID: 35732867 DOI: 10.1007/s12035-022-02922-3
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.682