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2019冠状病毒病的病毒学与分子发病机制:最新进展

Virology and Molecular Pathogenesis of Coronavirus Disease 2019: An Update.

作者信息

Panati Kalpana, Timmana Lokesh V, Reddy AT Venkatramana, Reddy Saddala Rajeswara, Ramireddy Narala Venkata

机构信息

Department of Biotechnology, Government College for Men, Kadapa, A.P, India

Department of Zoology, Yogi Vemana University, Kadapa, A.P, India

出版信息

Eurasian J Med. 2022 Oct;54(3):299-304. doi: 10.5152/eurasianjmed.2022.21133.

DOI:10.5152/eurasianjmed.2022.21133
PMID:35971283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9797742/
Abstract

The pandemic coronavirus disease 2019 outbreak's causative agent was identified as severe acute respiratory syndrome coronavirus 2. It is a positive-sense single-stranded RNA virus with a ~30 kb size genome that belongs to the Nidovirales. Molecular analysis revealed that severe acute respiratory syndrome coronavirus 2 is a variant of severe acute respiratory syndrome coronavirus and Middle East respiratory syndrome coronavirus with some sequence similarity. The confirmed cases and death toll are high in severe acute respiratory syndrome coronavirus 2 compared to severe acute respiratory syndrome coronavirus and the estimated R0 is >1. The data on pathological findings on severe acute respiratory syndrome coronavirus 2 are scarce and present treatment management is based on symptoms that are similar to severe acute respiratory syndrome coronavirus. In this review, we have discussed the transmission, viral replication, and cytokine storm and highlighted the recent pathological findings of coronavirus disease 2019. The reported severe acute respiratory syndrome coronavirus 2 pathological findings were similar to that of severe acute respiratory syndrome coronavirus. Though these findings help notify the clinical course of the disease, it warrants further in vivo and ex vivo studies with larger samples obtained from the coronavirus disease 2019 patients.

摘要

2019年大流行性冠状病毒病疫情的病原体被确定为严重急性呼吸综合征冠状病毒2。它是一种正链单链RNA病毒,基因组大小约为30 kb,属于尼多病毒目。分子分析显示,严重急性呼吸综合征冠状病毒2是严重急性呼吸综合征冠状病毒和中东呼吸综合征冠状病毒的变种,具有一些序列相似性。与严重急性呼吸综合征冠状病毒相比,严重急性呼吸综合征冠状病毒2的确诊病例和死亡人数较高,估计R0大于1。关于严重急性呼吸综合征冠状病毒2的病理结果的数据很少,目前的治疗管理是基于与严重急性呼吸综合征冠状病毒相似的症状。在这篇综述中,我们讨论了传播、病毒复制和细胞因子风暴,并强调了2019年冠状病毒病的最新病理结果。报告的严重急性呼吸综合征冠状病毒2的病理结果与严重急性呼吸综合征冠状病毒相似。尽管这些发现有助于了解疾病的临床过程,但仍需要对从2019年冠状病毒病患者中获得的更大样本进行进一步的体内和体外研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88eb/9797742/e21e11be8ab8/eajm-54-3-299_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88eb/9797742/9e1a864bea6f/eajm-54-3-299_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88eb/9797742/e21e11be8ab8/eajm-54-3-299_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88eb/9797742/9e1a864bea6f/eajm-54-3-299_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88eb/9797742/e21e11be8ab8/eajm-54-3-299_f002.jpg

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本文引用的文献

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Discoveries (Craiova). 2021 Mar 31;9(1):e126. doi: 10.15190/d.2021.5.
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Getting to the Heart of the Matter: Myocardial Injury, Coagulopathy, and Other Potential Cardiovascular Implications of COVID-19.直击问题核心:新型冠状病毒肺炎的心肌损伤、凝血功能障碍及其他潜在心血管影响
Int J Vasc Med. 2021 Apr 22;2021:6693895. doi: 10.1155/2021/6693895. eCollection 2021.
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Rise of the phoenix: Mucormycosis in COVID-19 times.
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Mutational heterogeneity in spike glycoproteins of severe acute respiratory syndrome coronavirus 2.严重急性呼吸综合征冠状病毒2刺突糖蛋白的突变异质性
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Casirivimab-imdevimab for Treatment of COVID-19 in Solid Organ Transplant Recipients: An Early Experience.卡西瑞维单抗-英夫西单抗用于实体器官移植受者治疗COVID-19:早期经验
Transplantation. 2021 Jul 1;105(7):e68-e69. doi: 10.1097/TP.0000000000003737.
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An overview of vaccine development for COVID-19.新冠病毒疫苗的开发概述。
Ther Deliv. 2021 Mar;12(3):235-244. doi: 10.4155/tde-2020-0129. Epub 2021 Feb 24.
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The Review of Histopathological Pulmonary Findings of COVID-19: What We Learned from Postmortem Biopsy and Autopsies; Beyond the Horizon.新型冠状病毒肺炎组织病理学肺部表现综述:我们从尸检活检和解剖中学到了什么;展望未来。
Eurasian J Med. 2020 Oct;52(3):307-308. doi: 10.5152/eurasianjmed.2020.20170.
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Coagulopathy, Venous Thromboembolism, and Anticoagulation in Patients with COVID-19.新型冠状病毒肺炎患者的凝血病、静脉血栓栓塞和抗凝治疗。
Pharmacotherapy. 2020 Nov;40(11):1130-1151. doi: 10.1002/phar.2465. Epub 2020 Nov 3.
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COVID-19: Coagulopathy, Risk of Thrombosis, and the Rationale for Anticoagulation.COVID-19:凝血功能障碍、血栓形成风险和抗凝治疗的理由。
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