• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

SARS-CoV-2:追溯起源,追踪进化。

SARS-CoV-2: tracing the origin, tracking the evolution.

机构信息

Department of Basic and Clinical Sciences, University of Nicosia Medical School, Nicosia, Cyprus.

出版信息

BMC Med Genomics. 2022 Mar 18;15(1):62. doi: 10.1186/s12920-022-01208-w.

DOI:10.1186/s12920-022-01208-w
PMID:35303887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8931788/
Abstract

The origin of SARS-CoV-2 is uncertain. Findings support a "bat origin" but results are not highly convincing. Studies found evidence that SARS-CoV-2 was around for many years before the pandemic outbreak. Evidence has been published that the progenitor of SARS-CoV-2 already had the capability to bind strongly to the human ACE2 receptor. This may be an indication that many other animal viruses are capable to jump to humans, having already affinity for a human receptor. This is quite worrying since current ecosystems' collapse brings people to high proximity with animals, increasing probabilities for random viral transitions. On the other hand, future adaptation of SARS-CoV-2 is of great concern. Virus-host interactions are complicated and unfortunately, we still do not have accurate tools for predicting viruses' future evolution. Viral adaptation is a multifactorial process and probably SARS-CoV-2 will not become soon, as we wish, a harmless infection. However, humanity is currently under the largest vaccination program and it's of great interest to see if vaccinations will change the evolutionary game against the virus.

摘要

新冠病毒(SARS-CoV-2)的起源尚不确定。有研究结果支持其“源自蝙蝠”,但说服力不够强。有研究发现,在此次大流行爆发之前,SARS-CoV-2 已经存在多年。有证据表明,SARS-CoV-2 的祖先进化而来的病毒株已经具备与人类 ACE2 受体强力结合的能力。这表明,许多其他动物病毒也有可能感染人类,因为它们已经对人类受体具有亲和力。鉴于当前生态系统的崩溃使人类与动物更加接近,增加了随机病毒传播的可能性,这种情况令人担忧。另一方面,人们非常关注 SARS-CoV-2 的未来适应性。病毒与宿主的相互作用非常复杂,不幸的是,我们仍然没有准确的工具来预测病毒未来的进化。病毒适应是一个多因素的过程,SARS-CoV-2 可能不会像我们希望的那样很快成为一种无害的感染。然而,人类目前正在实施有史以来最大规模的疫苗接种计划,人们非常关注疫苗接种是否会改变与病毒的进化博弈。

相似文献

1
SARS-CoV-2: tracing the origin, tracking the evolution.SARS-CoV-2:追溯起源,追踪进化。
BMC Med Genomics. 2022 Mar 18;15(1):62. doi: 10.1186/s12920-022-01208-w.
2
SARS-CoV-2 Evolutionary Adaptation toward Host Entry and Recognition of Receptor O-Acetyl Sialylation in Virus-Host Interaction.SARS-CoV-2 进化适应宿主进入和识别病毒-宿主相互作用中受体 O-乙酰神经氨酸糖基化。
Int J Mol Sci. 2020 Jun 26;21(12):4549. doi: 10.3390/ijms21124549.
3
The expression of hACE2 receptor protein and its involvement in SARS-CoV-2 entry, pathogenesis, and its application as potential therapeutic target.hACE2 受体蛋白的表达及其在 SARS-CoV-2 进入、发病机制中的作用及其作为潜在治疗靶点的应用。
Tumour Biol. 2021;43(1):177-196. doi: 10.3233/TUB-200084.
4
[Source of the COVID-19 pandemic: ecology and genetics of coronaviruses (Betacoronavirus: Coronaviridae) SARS-CoV, SARS-CoV-2 (subgenus Sarbecovirus), and MERS-CoV (subgenus Merbecovirus).].[新冠疫情的源头:冠状病毒(β冠状病毒:冠状病毒科)、严重急性呼吸综合征冠状病毒(SARS-CoV)、严重急性呼吸综合征冠状病毒2(SARS-CoV-2,Sarbecovirus亚属)和中东呼吸综合征冠状病毒(MERS-CoV,Merbecovirus亚属)的生态学与遗传学。]
Vopr Virusol. 2020;65(2):62-70. doi: 10.36233/0507-4088-2020-65-2-62-70.
5
In silico studies on the comparative characterization of the interactions of SARS-CoV-2 spike glycoprotein with ACE-2 receptor homologs and human TLRs.基于 SARS-CoV-2 刺突糖蛋白与 ACE-2 受体同源物和人类 TLR 相互作用的比较特征的计算机研究。
J Med Virol. 2020 Oct;92(10):2105-2113. doi: 10.1002/jmv.25987. Epub 2020 May 17.
6
Molecular evolution and phylogenetic analysis of SARS-CoV-2 and hosts ACE2 protein suggest Malayan pangolin as intermediary host.SARS-CoV-2 与宿主 ACE2 蛋白的分子进化和系统发育分析提示马来穿山甲可能为中间宿主。
Braz J Microbiol. 2020 Dec;51(4):1593-1599. doi: 10.1007/s42770-020-00321-1. Epub 2020 Jun 26.
7
Molecular dynamic simulation analysis of SARS-CoV-2 spike mutations and evaluation of ACE2 from pets and wild animals for infection risk.SARS-CoV-2 刺突突变的分子动力学模拟分析及宠物和野生动物 ACE2 感染风险评估。
Comput Biol Chem. 2022 Feb;96:107613. doi: 10.1016/j.compbiolchem.2021.107613. Epub 2021 Dec 1.
8
Evaluating angiotensin-converting enzyme 2-mediated SARS-CoV-2 entry across species.评估血管紧张素转化酶 2 介导的 SARS-CoV-2 在物种间的进入。
J Biol Chem. 2021 Jan-Jun;296:100435. doi: 10.1016/j.jbc.2021.100435. Epub 2021 Feb 19.
9
Impact of Genetic Variability in ACE2 Expression on the Evolutionary Dynamics of SARS-CoV-2 Spike D614G Mutation.ACE2 表达中的遗传变异性对 SARS-CoV-2 刺突 D614G 突变进化动态的影响。
Genes (Basel). 2020 Dec 24;12(1):16. doi: 10.3390/genes12010016.
10
Mutational landscape and in silico structure models of SARS-CoV-2 spike receptor binding domain reveal key molecular determinants for virus-host interaction.SARS-CoV-2 刺突受体结合域的突变景观和计算机结构模型揭示了病毒-宿主相互作用的关键分子决定因素。
BMC Mol Cell Biol. 2022 Jan 7;23(1):2. doi: 10.1186/s12860-021-00403-4.

引用本文的文献

1
The Batalogue: an overview of betacoronaviruses with future pandemic potential.《目录:具有未来大流行潜力的β冠状病毒概述》
FEMS Microbiol Rev. 2025 Jan 14;49. doi: 10.1093/femsre/fuaf023.
2
RAB5 is a host dependency factor for the generation of SARS-CoV-2 replication organelles.RAB5是新冠病毒复制细胞器生成的宿主依赖因子。
mBio. 2025 May 14;16(5):e0331424. doi: 10.1128/mbio.03314-24. Epub 2025 Apr 1.
3
Genetic diversity and genomic epidemiology of SARS-CoV-2 during the first 3 years of the pandemic in Morocco: comprehensive sequence analysis, including the unique lineage B.1.528 in Morocco.摩洛哥疫情头三年期间严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的遗传多样性和基因组流行病学:全面序列分析,包括摩洛哥独特的B.1.528谱系
Access Microbiol. 2024 Oct 7;6(10). doi: 10.1099/acmi.0.000853.v4. eCollection 2024.
4
Neutrophil Activity and Extracellular Matrix Degradation: Drivers of Lung Tissue Destruction in Fatal COVID-19 Cases and Implications for Long COVID.中性粒细胞活性和细胞外基质降解:致死性 COVID-19 病例中肺组织破坏的驱动因素及对长新冠的影响。
Biomolecules. 2024 Feb 17;14(2):236. doi: 10.3390/biom14020236.
5
Features of SARS-CoV-2 Replication in Various Types of Reptilian and Fish Cell Cultures.各种类型的爬行动物和鱼类细胞培养物中 SARS-CoV-2 的复制特征。
Viruses. 2023 Nov 29;15(12):2350. doi: 10.3390/v15122350.
6
Analyses of S Protein Homology Using the Genomes of SARS-CoV-2 Specimens Unveil Missing Links in the Temporal Order of Mutations in Its Variants.利用 SARS-CoV-2 样本的基因组进行 S 蛋白同源性分析揭示了其变异体中突变的时间顺序中的缺失环节。
Viruses. 2023 Oct 30;15(11):2182. doi: 10.3390/v15112182.
7
Have Diagnostics, Therapies, and Vaccines Made the Difference in the Pandemic Evolution of COVID-19 in Comparison with "Spanish Flu"?与“西班牙流感”相比,诊断方法、治疗手段和疫苗对新冠疫情演变产生了影响吗?
Pathogens. 2023 Jun 23;12(7):868. doi: 10.3390/pathogens12070868.
8
Role of Spillover and Spillback in SARS-CoV-2 Transmission and the Importance of One Health in Understanding the Dynamics of the COVID-19 Pandemic.人畜共患病溢出和回溢在 SARS-CoV-2 传播中的作用,以及在理解 COVID-19 大流行动态方面的“One Health”理念的重要性。
J Clin Microbiol. 2023 Jul 20;61(7):e0161022. doi: 10.1128/jcm.01610-22. Epub 2023 Apr 26.
9
Functional evolution of SARS-CoV-2 spike protein: Maintaining wide host spectrum and enhancing infectivity via surface charge of spike protein.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白的功能进化:通过刺突蛋白的表面电荷维持广泛宿主谱并增强传染性
Comput Struct Biotechnol J. 2023;21:2068-2074. doi: 10.1016/j.csbj.2023.03.010. Epub 2023 Mar 12.
10
Immunological Studies to Understand Hybrid/Recombinant Variants of SARS-CoV-2.旨在了解新冠病毒杂交/重组变体的免疫学研究。
Vaccines (Basel). 2022 Dec 25;11(1):45. doi: 10.3390/vaccines11010045.

本文引用的文献

1
Exploring the Natural Origins of SARS-CoV-2 in the Light of Recombination.在重组的背景下探索 SARS-CoV-2 的自然起源。
Genome Biol Evol. 2022 Feb 4;14(2). doi: 10.1093/gbe/evac018.
2
ACE2 binding is an ancestral and evolvable trait of sarbecoviruses.ACE2 结合是沙贝病毒科的一个祖传且可进化的特征。
Nature. 2022 Mar;603(7903):913-918. doi: 10.1038/s41586-022-04464-z. Epub 2022 Feb 3.
3
The Remarkable Evolutionary Plasticity of Coronaviruses by Mutation and Recombination: Insights for the COVID-19 Pandemic and the Future Evolutionary Paths of SARS-CoV-2.冠状病毒通过突变和重组实现的惊人进化可塑性:对 COVID-19 大流行及 SARS-CoV-2 未来进化路径的启示。
Viruses. 2022 Jan 2;14(1):78. doi: 10.3390/v14010078.
4
The pandemic's true death toll: millions more than official counts.疫情的真实死亡人数:比官方统计多出数百万。
Nature. 2022 Jan;601(7893):312-315. doi: 10.1038/d41586-022-00104-8.
5
Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa.南非 SARS-CoV-2 奥密克戎变异株的快速流行扩张。
Nature. 2022 Mar;603(7902):679-686. doi: 10.1038/s41586-022-04411-y. Epub 2022 Jan 7.
6
Beyond Omicron: what's next for COVID's viral evolution.超越奥密克戎:新冠病毒进化的下一步是什么
Nature. 2021 Dec;600(7888):204-207. doi: 10.1038/d41586-021-03619-8.
7
Where did 'weird' Omicron come from?“诡异”的奥密克戎毒株源自何处?
Science. 2021 Dec 3;374(6572):1179. doi: 10.1126/science.acx9738. Epub 2021 Dec 2.
8
Phylogenetic and Ancestral Sequence Reconstruction of SARS-CoV-2 Reveals Latent Capacity to Bind Human ACE2 Receptor.SARS-CoV-2 的系统发生和祖先序列重建揭示了潜在的与人 ACE2 受体结合的能力。
J Mol Evol. 2021 Dec;89(9-10):656-664. doi: 10.1007/s00239-021-10034-0. Epub 2021 Nov 5.
9
The Neighborhood of the Spike Gene Is a Hotspot for Modular Intertypic Homologous and Nonhomologous Recombination in Coronavirus Genomes.刺突基因附近是冠状病毒基因组中模块间异源和非同源重组的热点区域。
Mol Biol Evol. 2022 Jan 7;39(1). doi: 10.1093/molbev/msab292.
10
Dating the Common Ancestor from an NCBI Tree of 83688 High-Quality and Full-Length SARS-CoV-2 Genomes.从 83688 个高质量和全长 SARS-CoV-2 基因组的 NCBI 树中追溯共同祖先。
Viruses. 2021 Sep 8;13(9):1790. doi: 10.3390/v13091790.