Zika virus disrupts molecular fingerprinting of human neurospheres

Patrícia P. Garcez(Universidade Federal do Rio de Janeiro), Juliana Nascimento(Universidade Estadual de Campinas (UNICAMP)), Janaína Mota de Vasconcelos(Instituto Evandro Chagas), Rodrigo Madeiro da Costa(D’Or Institute for Research and Education), Rodrigo Delvecchio(Universidade Federal do Rio de Janeiro), Pablo Trindade(D’Or Institute for Research and Education), Erick Correia Loiola(D’Or Institute for Research and Education), Luiza M. Higa(Universidade Federal do Rio de Janeiro), Juliana S. Cassoli(Universidade Estadual de Campinas (UNICAMP)), Gabriela Vitória(D’Or Institute for Research and Education), Patrícia Carvalho de Sequeira(Fundação Oswaldo Cruz), Jaroslaw Sochacki(D’Or Institute for Research and Education), Renato Santana Aguiar(Universidade Federal do Rio de Janeiro), Hellen Thaís Fuzii(Universidade Federal do Pará), Ana María Bispo de Filippis(Fundação Oswaldo Cruz), João Lídio da Silva Gonçalves Vianez Júnior(Instituto Evandro Chagas), Amílcar Tanuri(Universidade Federal do Rio de Janeiro), Daniel Martins‐de‐Souza(Universidade Estadual de Campinas (UNICAMP)), Stevens K. Rehen(Universidade Federal do Rio de Janeiro)
Scientific Reports
January 23, 2017
Cited by 122Open Access
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Abstract

Zika virus (ZIKV) has been associated with microcephaly and other brain abnormalities; however, the molecular consequences of ZIKV to human brain development are still not fully understood. Here we describe alterations in human neurospheres derived from induced pluripotent stem (iPS) cells infected with the strain of Zika virus that is circulating in Brazil. Combining proteomics and mRNA transcriptional profiling, over 500 proteins and genes associated with the Brazilian ZIKV infection were found to be differentially expressed. These genes and proteins provide an interactome map, which indicates that ZIKV controls the expression of RNA processing bodies, miRNA biogenesis and splicing factors required for self-replication. It also suggests that impairments in the molecular pathways underpinning cell cycle and neuronal differentiation are caused by ZIKV. These results point to biological mechanisms implicated in brain malformations, which are important to further the understanding of ZIKV infection and can be exploited as therapeutic potential targets to mitigate it.


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