Department of Biochemistry, School of Life Sciences, Nanjing Normal University, Nanjing 210023, China.
COVID-19 Research Center, Institute of Laboratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing University and Southern Medical University, Nanjing 210002, China.
Bioinformatics. 2021 Jan 29;36(21):5133-5138. doi: 10.1093/bioinformatics/btaa725.
There are seven known coronaviruses that infect humans: four mild coronaviruses, including HCoV-229E, HCoV-OC43, HCoV-NL63 and HCoV-HKU1, only cause mild respiratory diseases, and three severe coronaviruses, including SARS-CoV, MERS-CoV and SARS-CoV-2, can cause severe respiratory diseases even death of infected patients. Both infection and death caused by SARS-CoV-2 are still rapidly increasing worldwide. In this study, we demonstrate that viral coding proteins of SARS-CoV-2 have distinct features and are most, medium and least conserved with SARS-CoV, MERS-CoV and the rest four mild coronaviruses (HCoV-229E, HCoV-OC43, HCoV-NL63 and HCoV-HKU1), respectively. Moreover, expression of host responsive genes (HRG), HRG-enriched biological processes and HRG-enriched KEGG pathways upon infection of SARS-CoV-2 shows slightly overlapping with SARS-CoV and MERS-CoV but distinctive to the four mild coronaviruses. Interestingly, enrichment of overactivation of neutrophil by HRGs is only and commonly found in infections of severe SARS-CoV-2, SARS-CoV and MERS-CoV but not in the other four mild coronaviruses, and the related gene networks show different patterns. Clinical data support that overactivation of neutrophil for severe patients can be one major factor for the similar clinical symptoms observed in SARS-CoV-2 infection compared to infections of the other two severe coronavirus (SARS-CoV and MERS-CoV). Taken together, our study provides a mechanistic insight into SARS-CoV-2 epidemic via revealing the conserved and distinct features of SARS-CoV-2, raising the critical role of dysregulation of neutrophil for SARS-CoV-2 infection.
All data sources and analysis methods related to this manuscript are available in the methods, supplementary materials and GEO database (https://www.ncbi.nlm.nih.gov/geo/).
Supplementary data are available at Bioinformatics online.
目前已知有七种可感染人类的冠状病毒:其中四种为温和冠状病毒,包括 HCoV-229E、HCoV-OC43、HCoV-NL63 和 HCoV-HKU1,仅引起轻微的呼吸道疾病;另外三种为严重冠状病毒,包括 SARS-CoV、MERS-CoV 和 SARS-CoV-2,可导致严重的呼吸道疾病甚至感染患者死亡。目前,SARS-CoV-2 的感染和死亡人数仍在全球范围内迅速增加。在本研究中,我们证明了 SARS-CoV-2 的病毒编码蛋白具有独特的特征,分别与 SARS-CoV、MERS-CoV 和另外四种温和冠状病毒(HCoV-229E、HCoV-OC43、HCoV-NL63 和 HCoV-HKU1)具有最大、中等和最小的保守性。此外,SARS-CoV-2 感染后宿主反应基因(HRG)的表达、HRG 富集的生物学过程和 HRG 富集的 KEGG 途径显示与 SARS-CoV 和 MERS-CoV 略有重叠,但与另外四种温和冠状病毒明显不同。有趣的是,HRG 引起的中性粒细胞过度激活仅在 SARS-CoV-2、SARS-CoV 和 MERS-CoV 的严重感染中普遍存在,而在另外四种温和冠状病毒中则不存在,且相关基因网络显示出不同的模式。临床数据支持,严重患者中性粒细胞的过度激活可能是 SARS-CoV-2 感染与另外两种严重冠状病毒(SARS-CoV 和 MERS-CoV)感染观察到相似临床症状的一个主要因素。综上所述,本研究通过揭示 SARS-CoV-2 的保守和独特特征,为 SARS-CoV-2 流行提供了一种机制上的见解,提出了中性粒细胞失调对 SARS-CoV-2 感染的关键作用。
本文涉及的所有数据源和分析方法均可在方法、补充材料和 GEO 数据库(https://www.ncbi.nlm.nih.gov/geo/)中获得。
补充数据可在生物信息学在线获得。