Su Kunkai, Huang Xin, Xu Kaijin, Du Weibo, Zhu Danhua, Yang Meifang, Yuan Wenji, Li Lanjuan
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
KS and XH contributed equally to this study.
Infect Microbes Dis. 2020 May 6;2(2):42-47. doi: 10.1097/IM9.0000000000000025. eCollection 2020 Jun.
The pandemic of coronavirus disease 2019 (COVID-19), a respiratory disease caused by a novel severe acute respiratory syndrome coronavirus-2, is causing substantial morbidity and mortality. Along with the respiratory symptoms, underlying diseases in senior patients, such as diabetes, hypertension, and coronary heart disease, are the most common comorbidities, which cause more severe outcomes and even death. During cellular attachment and entry of severe acute respiratory syndrome coronavirus-2, the key protein involved is the angiotensin I converting enzyme 2 (ACE2), which is located on the membrane of host cells. Here, we aim to curate an expression profile of and other COVID-19 related genes across the available diabetes murine strains. Based on strictly manual curation and bioinformatics analysis of the publicly deposited expression datasets, and other potentially involved genes such as , , , and were examined. We found that expression is rather ubiquitous in three selected diabetes prone strains (db/db, ob/ob and diet-induced obese). With the most abundant datasets present, the liver shows a medium expression level compared with the lungs, pancreatic islets, brain and even T cells. Age is a more critical factor for expression in db/db compared with the other two strains. Besides , the other four host genes showed varied levels of correlation to each other. To accelerate research on the interaction between COVID-19 and underlying diseases, the Murine4Covid transcriptomics database (www.geneureka.org/Murine4Covid) will facilitate the design of research on COVID-19 and comorbidities.
2019冠状病毒病(COVID-19)大流行,这是一种由新型严重急性呼吸综合征冠状病毒2引起的呼吸道疾病,正在导致大量发病和死亡。除呼吸道症状外,老年患者的基础疾病,如糖尿病、高血压和冠心病,是最常见的合并症,这些疾病会导致更严重的后果甚至死亡。在严重急性呼吸综合征冠状病毒2的细胞附着和进入过程中,涉及的关键蛋白是血管紧张素I转换酶2(ACE2),它位于宿主细胞膜上。在此,我们旨在梳理出在现有糖尿病小鼠品系中ACE2及其他与COVID-19相关基因的表达谱。基于对公开存放的表达数据集进行严格的人工整理和生物信息学分析,对ACE2及其他潜在相关基因,如[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]进行了研究。我们发现,ACE2在三种选定的糖尿病易患品系(db/db、ob/ob和饮食诱导肥胖)中表达相当普遍。由于存在最丰富的数据集,与肺、胰岛、脑甚至T细胞相比,肝脏显示出中等水平的ACE2表达。与其他两个品系相比,年龄是db/db品系中ACE2表达的一个更关键因素。除ACE2外,其他四个宿主基因彼此之间呈现出不同程度的相关性。为了加速对COVID-19与基础疾病之间相互作用的研究,小鼠4Covid转录组学数据库(www.geneureka.org/Murine4Covid)将有助于设计关于COVID-19与合并症的研究。