ICMR-Laboratory, ICMR-NICED, P-33, C.I.T. Road, Scheme XM, Beliaghata, Kolkata, West Bengal 700010, India.
Department of Cell Biology and Physiology, CSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal 700032, India.
J Proteome Res. 2024 Sep 6;23(9):3731-3745. doi: 10.1021/acs.jproteome.3c00751. Epub 2024 Aug 12.
Dengue fever is a rapidly emerging tropical disease and an important cause of morbidity in its severe form worldwide. A wide spectrum of the pathophysiology is associated with the transition of dengue fever to severe dengue, which is driven by the host immune response and might reflect in patients' proteome profile. This study aims to analyze the plasma from different phases of dengue-infected patients at two time points. A mass-spectrometry-based proteomic approach was utilized to understand the involvement of probable candidate proteins toward developing a more severe, hemorrhagic form of dengue fever. Dengue-infected hospital-admitted patients with <5 days of fever were included in this study. Patient samples from the acute phase were screened for the presence of NS1 antigen using ELISA and subjected to molecular serotyping. Dengue molecular serotype-confirmed patient samples, pairwise from acute and critical phases with healthy control were subjected to qualitative and quantitative proteomic analysis, and then pathway analysis was performed. The protein-protein interaction network between the dengue virus and host proteins was depicted in the search for proteins associated with severe dengue pathophysiology. An array of apolipoprotein, cytokines, and endothelial proteins in association with virus replication and endothelial dysfunction were validated as biomolecules involved in severe dengue pathophysiology.
登革热是一种迅速出现的热带病,也是全球严重形式下发病率的重要原因。广泛的病理生理学与登革热向重症登革热的转变有关,这是由宿主免疫反应驱动的,可能反映在患者的蛋白质组谱中。本研究旨在分析两个时间点不同阶段感染登革热患者的血浆。利用基于质谱的蛋白质组学方法来了解可能的候选蛋白的参与,以开发更严重的出血性登革热形式。本研究纳入了发热<5 天的住院登革热感染患者。使用 ELISA 筛选急性阶段患者样本中是否存在 NS1 抗原,并进行分子血清型鉴定。对急性和危急阶段与健康对照组的登革分子血清型确认患者样本进行定性和定量蛋白质组学分析,然后进行途径分析。描绘了登革病毒和宿主蛋白之间的蛋白质-蛋白质相互作用网络,以寻找与重症登革热病理生理学相关的蛋白质。一系列载脂蛋白、细胞因子和内皮蛋白与病毒复制和内皮功能障碍相关,被验证为重症登革热病理生理学相关的生物分子。