| Literature DB >> 30377986 |
Walter O Beys-da-Silva1,2, Rafael L Rosa3,4, Lucélia Santi5,3, Markus Berger3, Sung Kyu Park6, Alexandre R Campos7, Paula Terraciano3, Ana Paula M Varela8, Thais F Teixeira8, Paulo M Roehe9, André Quincozes-Santos10, John R Yates6, Diogo O Souza10, Elizabeth O Cirne-Lima3,11,12, Jorge A Guimarães13,14.
Abstract
The recent microcephaly outbreak in Brazil has been associated with Zika virus (ZIKV) infection. The current understanding of damage caused by ZIKV infection is still unclear, since it has been implicated in other neurodegenerative and developmental complications. Here, the differential proteome analysis of human mesenchymal stem cells (hMSC) infected with a Brazilian strain of ZIKV was identified by shotgun proteomics (MudPIT). Our results indicate that ZIKV induces a potential reprogramming of the metabolic machinery in nucleotide metabolism, changes in the energy production via glycolysis and other metabolic pathways, and potentially inhibits autophagy, neurogenesis, and immune response by downregulation of signaling pathways. In addition, proteins previously described in several brain pathologies, such as Alzheimer's disease, autism spectrum disorder, amyotrophic lateral sclerosis, and Parkinson's disease, were found with altered expression due to ZIKV infection in hMSC. This potential link between ZIKV and several neuropathologies beyond microcephaly is being described here for the first time and can be used to guide specific follow-up studies concerning these specific diseases and ZIKV infection.Entities:
Keywords: Brain diseases; Human mesenchymal stem cells; Microcephaly; Proteome; Zika virus
Mesh:
Substances:
Year: 2018 PMID: 30377986 PMCID: PMC6491274 DOI: 10.1007/s12035-018-1417-x
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590