Proteomics Unit, Department of Biochemistry, Institute of Chemistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-909, Brazil.
Laboratory of Proteomics (LabProt), LADETEC, Institute of Chemistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-598, Brazil.
J Proteome Res. 2024 Apr 5;23(4):1200-1220. doi: 10.1021/acs.jproteome.3c00677. Epub 2024 Feb 23.
The Zika virus (ZIKV) can be vertically transmitted, causing congenital Zika syndrome (CZS) in fetuses. ZIKV infection in early gestational trimesters increases the chances of developing CZS. This syndrome involves several pathologies with a complex diagnosis. In this work, we aim to identify biological processes and molecular pathways related to CZS and propose a series of putative protein and metabolite biomarkers for CZS prognosis in early pregnancy trimesters. We analyzed serum samples of healthy pregnant women and ZIKV-infected pregnant women bearing nonmicrocephalic and microcephalic fetuses. A total of 1090 proteins and 512 metabolites were identified by bottom-up proteomics and untargeted metabolomics, respectively. Univariate and multivariate statistical approaches were applied to find CZS differentially abundant proteins (DAP) and metabolites (DAM). Enrichment analysis (i.e., biological processes and molecular pathways) of the DAP and the DAM allowed us to identify the ECM organization and proteoglycans, amino acid metabolism, and arachidonic acid metabolism as CZS signatures. Five proteins and four metabolites were selected as CZS biomarker candidates. Serum multiomics analysis led us to propose nine putative biomarkers for CZS prognosis with high sensitivity and specificity.
寨卡病毒(ZIKV)可垂直传播,导致胎儿先天性寨卡综合征(CZS)。妊娠期前三个月的 ZIKV 感染增加了发生 CZS 的可能性。该综合征涉及多种具有复杂诊断的病理学。在这项工作中,我们旨在确定与 CZS 相关的生物学过程和分子途径,并提出一系列用于预测早孕期 CZS 的潜在蛋白质和代谢物生物标志物。我们分析了健康孕妇和携带非小头畸形及小头畸形胎儿的寨卡病毒感染孕妇的血清样本。通过靶向蛋白质组学和非靶向代谢组学分别鉴定出了 1090 种蛋白质和 512 种代谢物。应用单变量和多变量统计方法来寻找 CZS 差异丰度蛋白(DAP)和代谢物(DAM)。对 DAP 和 DAM 的富集分析(即生物学过程和分子途径)使我们能够确定 ECM 组织和蛋白聚糖、氨基酸代谢和花生四烯酸代谢是 CZS 的特征。选择了 5 种蛋白质和 4 种代谢物作为 CZS 生物标志物候选物。血清多组学分析使我们提出了 9 种具有高灵敏度和特异性的用于预测 CZS 的潜在生物标志物。