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Re-analysis of SARS-CoV-2-infected host cell proteomics time-course data by impact pathway analysis and network analysis: a potential link with inflammatory response

机译:通过影响途径分析和网络分析重新分析SARS-CoV-2感染的宿主细胞蛋白质组学时程数据:与炎症反应的潜在联系

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摘要

Coronavirus disease 2019 (COVID-19), caused by an outbreak of the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) in Wuhan, China, has led to an unprecedented health and economic crisis worldwide. To develop treatments that can stop or lessen the symptoms and severity of SARS-CoV-2 infection, it is critical to understand how the virus behaves inside human cells, and so far studies in this area remain scarce. A recent study investigated translatome and proteome host cell changes induced by SARS-CoV-2. Here, we use the publicly available proteomics data from this study to re-analyze the cellular consequences of SARS-CoV-2 infection by impact pathways analysis and network analysis. Notably, proteins linked to the inflammatory response, but also proteins related to chromosome segregation during mitosis, were found to be altered in response to viral infection. Upregulation of inflammatory response proteins is in line with the propagation of inflammatory reaction and lung injury that is observed in advanced stages of COVID-19 patients and which worsens with age.
机译:在中国武汉爆发的严重急性呼吸系统综合症冠状病毒2(SARS-CoV-2)引起的冠状病毒病2019(COVID-19)已导致全球范围内前所未有的健康和经济危机。为了开发出可以停止或减轻SARS-CoV-2感染的症状和严重程度的治疗方法,至关重要的是要了解该病毒在人体细胞内部的行为方式,迄今为止,在这一领域的研究仍然很少。最近的研究调查了SARS-CoV-2诱导的转录组和蛋白质组宿主细胞的变化。在这里,我们使用来自这项研究的公共蛋白质组学数据,通过影响途径分析和网络分析来重新分析SARS-CoV-2感染的细胞后果。值得注意的是,发现与炎症反应相关的蛋白质,以及与有丝分裂过程中与染色体分离有关的蛋白质,都可以响应病毒感染而发生改变。炎性反应蛋白的上调与在COVID-19患者的晚期观察到的炎性反应和肺损伤的传播相一致,并且随着年龄的增长而恶化。

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