• 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

全球 SARS-CoV-2 刺突蛋白受体结合域中适应性和持续性感染突变的流行情况。

Global Prevalence of Adaptive and Prolonged Infections' Mutations in the Receptor-Binding Domain of the SARS-CoV-2 Spike Protein.

机构信息

Department of Medical Sciences, Section of Clinical Microbiology, Uppsala University, 751 85 Uppsala, Sweden.

Chester Medical School, University of Chester, Chester CH2 1BR, UK.

出版信息

Viruses. 2021 Sep 30;13(10):1974. doi: 10.3390/v13101974.

DOI:10.3390/v13101974
PMID:34696404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8538289/
Abstract

Several vaccines with varying efficacies have been developed and are currently administered globally to minimize the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Despite having an RNA-dependent RNA polymerase with a proofreading activity, new variants of SARS-CoV-2 are on the rise periodically. Some of the mutations in these variants, especially mutations on the spike protein, aid the virus in transmission, infectivity and host immune evasion. Further, these mutations also reduce the effectiveness of some of the current vaccines and monoclonal antibodies (mAbs). In the present study, using the available 984,769 SARS-CoV-2 nucleotide sequences on the NCBI database from the end of 2019 till 28 July 2021, we have estimated the global prevalence of so-called 'adaptive mutations' and 'mutations identified in the prolonged infections', in the receptor-binding domain (RBD) of the spike (S) protein. Irrespective of the geographical region, in the case of the adaptive mutations, N501Y (48.38%) was found to be the dominant mutation followed by L452R (17.52%), T478K (14.31%), E484K (4.69%), S477N (3.29%), K417T (1.64%), N439K (0.7%) and S494P (0.7%). Other mutations were found to be less prevalent (less than 0.7%). Since the last two months, there has been a massive increase of L452R and T478K mutations (delta variant) in certain areas. In the case of prolonged infections' mutations (long-term SARS-CoV-2 infections), V483A (0.009%) was found to be dominant followed by Q493R (0.009%), while other mutations were found in less than 0.007% of the studied sequences. The data obtained in this study will aid in the development of better infection control policies, thereby curbing the spread of this virus.

摘要

已经开发出了几种具有不同功效的疫苗,目前正在全球范围内使用,以最大限度地减少严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的传播。尽管具有具有校对活性的 RNA 依赖性 RNA 聚合酶,但 SARS-CoV-2 的新变体仍在定期出现。这些变体中的一些突变,特别是刺突蛋白上的突变,有助于病毒传播、感染性和宿主免疫逃逸。此外,这些突变还降低了一些当前疫苗和单克隆抗体(mAbs)的有效性。在本研究中,使用 NCBI 数据库中 2019 年底至 2021 年 7 月 28 日期间可用的 984,769 个 SARS-CoV-2 核苷酸序列,我们估计了 Spike(S)蛋白受体结合域(RBD)中所谓的“适应性突变”和“在长时间感染中鉴定出的突变”的全球流行率。无论地理位置如何,在适应性突变的情况下,发现 N501Y(48.38%)是主要突变,其次是 L452R(17.52%)、T478K(14.31%)、E484K(4.69%)、S477N(3.29%)、K417T(1.64%)、N439K(0.7%)和 S494P(0.7%)。其他突变的发生率较低(低于 0.7%)。在过去的两个月中,某些地区 L452R 和 T478K 突变(delta 变体)大量增加。在长时间感染的突变(长期 SARS-CoV-2 感染)中,发现 V483A(0.009%)是主要突变,其次是 Q493R(0.009%),而其他突变的发生率低于研究序列的 0.007%。本研究获得的数据将有助于制定更好的感染控制政策,从而遏制该病毒的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbf2/8538289/36df1f2cde0c/viruses-13-01974-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbf2/8538289/b3b397d2bfbc/viruses-13-01974-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbf2/8538289/36df1f2cde0c/viruses-13-01974-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbf2/8538289/b3b397d2bfbc/viruses-13-01974-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbf2/8538289/36df1f2cde0c/viruses-13-01974-g002.jpg

相似文献

1
Global Prevalence of Adaptive and Prolonged Infections' Mutations in the Receptor-Binding Domain of the SARS-CoV-2 Spike Protein.全球 SARS-CoV-2 刺突蛋白受体结合域中适应性和持续性感染突变的流行情况。
Viruses. 2021 Sep 30;13(10):1974. doi: 10.3390/v13101974.
2
Vaccine-escape and fast-growing mutations in the United Kingdom, the United States, Singapore, Spain, India, and other COVID-19-devastated countries.疫苗逃逸和快速突变在英国、美国、新加坡、西班牙、印度和其他受 COVID-19 肆虐的国家。
Genomics. 2021 Jul;113(4):2158-2170. doi: 10.1016/j.ygeno.2021.05.006. Epub 2021 May 15.
3
Effects of common mutations in the SARS-CoV-2 Spike RBD and its ligand, the human ACE2 receptor on binding affinity and kinetics.常见突变对 SARS-CoV-2 刺突 RBD 及其配体人 ACE2 受体结合亲和力和动力学的影响。
Elife. 2021 Aug 26;10:e70658. doi: 10.7554/eLife.70658.
4
GB-2 blocking the interaction between ACE2 and wild type and mutation of spike protein of SARS-CoV-2.GB-2阻断ACE2与新型冠状病毒野生型及刺突蛋白突变体之间的相互作用。
Biomed Pharmacother. 2021 Oct;142:112011. doi: 10.1016/j.biopha.2021.112011. Epub 2021 Aug 5.
5
Variants of SARS-CoV-2, their effects on infection, transmission and neutralization by vaccine-induced antibodies.SARS-CoV-2 的变异体及其对感染、传播和疫苗诱导抗体中和作用的影响。
Eur Rev Med Pharmacol Sci. 2021 Sep;25(18):5857-5864. doi: 10.26355/eurrev_202109_26805.
6
RBD Double Mutations of SARS-CoV-2 Strains Increase Transmissibility through Enhanced Interaction between RBD and ACE2 Receptor.SARS-CoV-2 株的 RBD 双重突变通过增强 RBD 与 ACE2 受体之间的相互作用增加传染性。
Viruses. 2021 Dec 21;14(1):1. doi: 10.3390/v14010001.
7
Possible Link between Higher Transmissibility of Alpha, Kappa and Delta Variants of SARS-CoV-2 and Increased Structural Stability of Its Spike Protein and hACE2 Affinity.可能与 SARS-CoV-2 的 Alpha、Kappa 和 Delta 变体更高的传染性以及其刺突蛋白和 hACE2 亲和力的结构稳定性增加有关。
Int J Mol Sci. 2021 Aug 24;22(17):9131. doi: 10.3390/ijms22179131.
8
Comprehensive mapping of binding hot spots of SARS-CoV-2 RBD-specific neutralizing antibodies for tracking immune escape variants.全面绘制 SARS-CoV-2 RBD 特异性中和抗体的结合热点,用于跟踪免疫逃逸变异株。
Genome Med. 2021 Oct 14;13(1):164. doi: 10.1186/s13073-021-00985-w.
9
Receptor binding, immune escape, and protein stability direct the natural selection of SARS-CoV-2 variants.受体结合、免疫逃逸和蛋白稳定性指导 SARS-CoV-2 变体的自然选择。
J Biol Chem. 2021 Oct;297(4):101208. doi: 10.1016/j.jbc.2021.101208. Epub 2021 Sep 17.
10
A comprehensive overview of identified mutations in SARS CoV-2 spike glycoprotein among Iranian patients.伊朗患者中鉴定出的 SARS CoV-2 刺突糖蛋白突变的综合概述。
Gene. 2022 Mar 1;813:146113. doi: 10.1016/j.gene.2021.146113. Epub 2021 Dec 9.

引用本文的文献

1
Cell type-specific adaptation of the SARS-CoV-2 spike.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白的细胞类型特异性适应性
Virus Evol. 2024 Apr 25;10(1):veae032. doi: 10.1093/ve/veae032. eCollection 2024.
2
Prevalence of SARS-CoV-2 Omicron Sublineages and Spike Protein Mutations Conferring Resistance against Monoclonal Antibodies in a Swedish Cohort during 2022-2023.2022 - 2023年瑞典队列中严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎亚谱系及赋予对单克隆抗体抗性的刺突蛋白突变的流行情况
Microorganisms. 2023 Sep 27;11(10):2417. doi: 10.3390/microorganisms11102417.
3
Lessons learned and implications of early therapies for coronavirus disease in a territorial service centre in the Calabria region: a retrospective study.

本文引用的文献

1
The N501Y spike substitution enhances SARS-CoV-2 infection and transmission.N501Y 刺突突变增强了 SARS-CoV-2 的感染和传播。
Nature. 2022 Feb;602(7896):294-299. doi: 10.1038/s41586-021-04245-0. Epub 2021 Nov 24.
2
Molecular rationale for SARS-CoV-2 spike circulating mutations able to escape bamlanivimab and etesevimab monoclonal antibodies.SARS-CoV-2 刺突循环突变逃避巴美替尼和埃特司韦单抗单克隆抗体的分子原理。
Sci Rep. 2021 Oct 12;11(1):20274. doi: 10.1038/s41598-021-99827-3.
3
Detection and characterization of the SARS-CoV-2 lineage B.1.526 in New York.
卡拉布里亚地区一个地区服务中心的冠状病毒病早期治疗的经验教训和影响:一项回顾性研究。
BMC Infect Dis. 2022 Oct 20;22(1):793. doi: 10.1186/s12879-022-07774-9.
4
SARS-CoV-2 variants of concern and spike protein mutational dynamics in a Swedish cohort during 2021, studied by Nanopore sequencing.2021 年在瑞典队列中通过纳米孔测序研究的关注的 SARS-CoV-2 变体和刺突蛋白突变动态。
Virol J. 2022 Oct 18;19(1):164. doi: 10.1186/s12985-022-01896-x.
5
Dynamics of the interaction between the receptor-binding domain of SARS-CoV-2 Omicron (B.1.1.529) variant and human angiotensin-converting enzyme 2.SARS-CoV-2 奥密克戎(B.1.1.529)变体受体结合域与人血管紧张素转化酶 2 相互作用的动力学。
PeerJ. 2022 Jul 5;10:e13680. doi: 10.7717/peerj.13680. eCollection 2022.
6
Spike protein of SARS-CoV-2 variants: a brief review and practical implications.SARS-CoV-2 变体的刺突蛋白:简要综述及实际意义。
Braz J Microbiol. 2022 Sep;53(3):1133-1157. doi: 10.1007/s42770-022-00743-z. Epub 2022 Apr 9.
7
Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles.基于整合到慢病毒颗粒中的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白建立假病毒中和试验。
Biosaf Health. 2022 Feb;4(1):38-44. doi: 10.1016/j.bsheal.2021.12.006. Epub 2022 Jan 3.
8
COVID-19 in 2021.2021 年的 COVID-19。
Viruses. 2021 Oct 18;13(10):2098. doi: 10.3390/v13102098.
在纽约检测和描述 SARS-CoV-2 谱系 B.1.526。
Nat Commun. 2021 Aug 9;12(1):4886. doi: 10.1038/s41467-021-25168-4.
4
Affinity maturation of SARS-CoV-2 neutralizing antibodies confers potency, breadth, and resilience to viral escape mutations.SARS-CoV-2 中和抗体的亲和力成熟赋予了对病毒逃逸突变的效力、广度和恢复能力。
Immunity. 2021 Aug 10;54(8):1853-1868.e7. doi: 10.1016/j.immuni.2021.07.008. Epub 2021 Jul 30.
5
Effect of natural mutations of SARS-CoV-2 on spike structure, conformation, and antigenicity.SARS-CoV-2 天然突变对刺突结构、构象和抗原性的影响。
Science. 2021 Aug 6;373(6555). doi: 10.1126/science.abi6226. Epub 2021 Jun 24.
6
The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies.单克隆抗体组合药物 REGEN-COV 可预防 SARS-CoV-2 突变逃逸,这一结论在临床前和人体研究中得到验证。
Cell. 2021 Jul 22;184(15):3949-3961.e11. doi: 10.1016/j.cell.2021.06.002. Epub 2021 Jun 5.
7
E484K as an innovative phylogenetic event for viral evolution: Genomic analysis of the E484K spike mutation in SARS-CoV-2 lineages from Brazil.E484K 作为病毒进化的创新性进化事件:来自巴西的 SARS-CoV-2 谱系中 E484K 刺突突变的基因组分析。
Infect Genet Evol. 2021 Sep;93:104941. doi: 10.1016/j.meegid.2021.104941. Epub 2021 May 25.
8
SARS-CoV-2 mutations, vaccines, and immunity: implication of variants of concern.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)突变、疫苗与免疫:关注变异株的影响
Signal Transduct Target Ther. 2021 May 22;6(1):203. doi: 10.1038/s41392-021-00623-2.
9
Structural and functional ramifications of antigenic drift in recent SARS-CoV-2 variants.近期 SARS-CoV-2 变异株中抗原漂移的结构和功能影响。
Science. 2021 Aug 13;373(6556):818-823. doi: 10.1126/science.abh1139. Epub 2021 May 20.
10
Preliminary report on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Spike mutation T478K.关于严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突突变 T478K 的初步报告。
J Med Virol. 2021 Sep;93(9):5638-5643. doi: 10.1002/jmv.27062. Epub 2021 May 15.