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• W2328411724 abstract "Zika virus (ZIKV) infection during pregnancy may be linked to fetal neurological complications that include brain damage and microcephaly. How the viral infection relates to fetal brain malformations is unknown. This study analyzes ZIKV polyprotein for peptide sharing with human proteins that, when altered, associate with microcephaly and brain calcifications. Results highlight a vast viral versus human peptide commonality that, in particular, involves centriolar and centrosomal components canonically cataloged as microcephaly proteins, i.e., C2CD3, CASC5, CP131, GCP4, KIF2A, STIL, and TBG. Likewise, a search for ZIKV peptide occurrences in human proteins linked to Guillain-Barré-like syndromes also show a high, unexpected level of peptide sharing. Of note, further analyses using the Immune Epitope DataBase (IEDB) resource show that many of the shared peptides are endowed with immunological potential. The data indicate that immune reactions following ZIKV infection might be a considerable source of crossreactions with brain-specific proteins and might contribute to the ZIKV-associated neuropathologic sequelae." @default.
• W2328411724 created "2016-06-24" @default.
• W2328411724 creator A5000501446 @default.
• W2328411724 creator A5040099455 @default.
• W2328411724 date "2016-08-01" @default.
• W2328411724 modified "2023-10-16" @default.
• W2328411724 title "Zika virus and autoimmunity: From microcephaly to Guillain-Barré syndrome, and beyond" @default.
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• W2328411724 doi "https://doi.org/10.1016/j.autrev.2016.03.020" @default.
• W2328411724 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27019049" @default.
• W2328411724 hasPublicationYear "2016" @default.
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