Kumar Nilesh, Mishra Bharat, Mehmood Adeel
Department of Biology, University of Alabama at Birmingham, 464 Campbell Hall, 1300 University Boulevard, AL 35294, USA.
Department of Computer Science, University of Alabama at Birmingham, 1402 10th Avenue S., Birmingham, AL 35294, USA.
iScience. 2020 Sep 25;23(9):101526. doi: 10.1016/j.isci.2020.101526. Epub 2020 Sep 3.
COVID-19 (coronavirus disease 2019) is a respiratory illness caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although the pathophysiology of this virus is complex and largely unknown, we employed a network-biology-fueled approach and integrated transcriptome data pertaining to lung epithelial cells with human interactome to generate Calu-3-specific human-SARS-CoV-2 interactome (CSI). Topological clustering and pathway enrichment analysis show that SARS-CoV-2 targets central nodes of the host-viral network, which participate in core functional pathways. Network centrality analyses discover 33 high-value SARS-CoV-2 targets, which are possibly involved in viral entry, proliferation, and survival to establish infection and facilitate disease progression. Our probabilistic modeling framework elucidates critical regulatory circuitry and molecular events pertinent to COVID-19, particularly the host-modifying responses and cytokine storm. Overall, our network-centric analyses reveal novel molecular components, uncover structural and functional modules, and provide molecular insights into the pathogenicity of SARS-CoV-2 that may help foster effective therapeutic design.
2019冠状病毒病(COVID-19)是一种由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的呼吸道疾病。尽管这种病毒的病理生理学很复杂且很大程度上未知,但我们采用了一种由网络生物学推动的方法,将与肺上皮细胞相关的转录组数据与人类相互作用组整合,以生成Calu-3特异性的人类-SARS-CoV-2相互作用组(CSI)。拓扑聚类和通路富集分析表明,SARS-CoV-2靶向宿主-病毒网络的中心节点,这些节点参与核心功能通路。网络中心性分析发现了33个高价值的SARS-CoV-2靶点,它们可能参与病毒进入、增殖和存活以建立感染并促进疾病进展。我们的概率建模框架阐明了与COVID-19相关的关键调控电路和分子事件,特别是宿主修饰反应和细胞因子风暴。总体而言,我们以网络为中心的分析揭示了新的分子成分,发现了结构和功能模块,并提供了对SARS-CoV-2致病性的分子见解,这可能有助于促进有效的治疗设计。