• 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

冠状病毒全长基因组和缺陷型病毒基因组在不同选择压力下的刺突蛋白进化。

Evolution of the coronavirus spike protein in the full-length genome and defective viral genome under diverse selection pressures.

机构信息

Graduate Institute of Veterinary Pathobiology, College of Veterinary Medicine, National Chung Hsing University, Taichung 40227, Taiwan, ROC.

Department of Veterinary Medicine, College of Veterinary Medicine, National Chung Hsing University, Taichung 40227, Taiwan, ROC.

出版信息

J Gen Virol. 2023 Nov;104(11). doi: 10.1099/jgv.0.001920.

DOI:10.1099/jgv.0.001920
PMID:37997889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10768696/
Abstract

How coronaviruses evolve by altering the structures of their full-length genome and defective viral genome (DVG) under dynamic selection pressures has not been studied. In this study, we aimed to experimentally identify the dynamic evolutionary patterns of the S protein sequence in the full-length genome and DVG under diverse selection pressures, including persistence, innate immunity and antiviral drugs. The evolutionary features of the S protein sequence in the full-length genome and in the DVG under diverse selection pressures are as follows: (i) the number of nucleotide (nt) mutations does not necessarily increase with the number of selection pressures; (ii) certain types of selection pressure(s) can lead to specific nt mutations; (iii) the mutated nt sequence can be reverted to the wild-type nt sequence under the certain type of selection pressure(s); (iv) the DVG can also undergo mutations and evolve independently of the full-length genome; and (v) DVG species are regulated during evolution under diverse selection pressures. The various evolutionary patterns of the S protein sequence in the full-length genome and DVG identified in this study may contribute to coronaviral fitness under diverse selection pressures.

摘要

冠状病毒如何通过改变其全长基因组和缺陷型病毒基因组(DVG)的结构,在动态选择压力下进化,尚未得到研究。在这项研究中,我们旨在通过实验确定全长基因组和 DVG 中 S 蛋白序列在不同选择压力下(包括持续性、先天免疫和抗病毒药物)的动态进化模式。在不同选择压力下,全长基因组和 DVG 中 S 蛋白序列的进化特征如下:(i)核苷酸(nt)突变的数量不一定随选择压力的增加而增加;(ii)某些类型的选择压力可以导致特定的 nt 突变;(iii)在特定类型的选择压力下,突变的 nt 序列可以恢复为野生型 nt 序列;(iv)DVG 也可以独立于全长基因组发生突变和进化;以及(v)在不同选择压力下,DVG 物种在进化过程中受到调控。本研究中鉴定的全长基因组和 DVG 中 S 蛋白序列的各种进化模式可能有助于冠状病毒在不同选择压力下的适应性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/2c4f864d4ad5/jgv-104-1920-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/00454871072b/jgv-104-1920-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/63f5abddc494/jgv-104-1920-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/4d982c4b6f84/jgv-104-1920-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/5c58061c937f/jgv-104-1920-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/b7713c1bfadd/jgv-104-1920-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/9578cf5295d5/jgv-104-1920-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/2c4f864d4ad5/jgv-104-1920-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/00454871072b/jgv-104-1920-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/63f5abddc494/jgv-104-1920-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/4d982c4b6f84/jgv-104-1920-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/5c58061c937f/jgv-104-1920-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/b7713c1bfadd/jgv-104-1920-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/9578cf5295d5/jgv-104-1920-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a9/10768696/2c4f864d4ad5/jgv-104-1920-g007.jpg

相似文献

1
Evolution of the coronavirus spike protein in the full-length genome and defective viral genome under diverse selection pressures.冠状病毒全长基因组和缺陷型病毒基因组在不同选择压力下的刺突蛋白进化。
J Gen Virol. 2023 Nov;104(11). doi: 10.1099/jgv.0.001920.
2
Unveiling the biology of defective viral genomes in vitro and in vivo: implications for gene expression and pathogenesis of coronavirus.揭示缺陷型病毒基因组在体外和体内的生物学特性:对冠状病毒基因表达和发病机制的影响。
Virol J. 2023 Oct 6;20(1):225. doi: 10.1186/s12985-023-02189-7.
3
Bovine Coronavirus: Variability, Evolution, and Dispersal Patterns of a No Longer Neglected Betacoronavirus.牛冠状病毒:一种不再被忽视的β冠状病毒的变异性、进化和传播模式。
Viruses. 2020 Nov 10;12(11):1285. doi: 10.3390/v12111285.
4
Comparative analysis of the genome structure and organization of the Middle East respiratory syndrome coronavirus (MERS-CoV) 2012 to 2019 revealing evidence for virus strain barcoding, zoonotic transmission, and selection pressure.2012 年至 2019 年中东呼吸综合征冠状病毒(MERS-CoV)基因组结构和组织的比较分析显示了病毒株条形码、人畜共患传播和选择压力的证据。
Rev Med Virol. 2021 Jan;31(1):1-12. doi: 10.1002/rmv.2150. Epub 2020 Aug 17.
5
Identification of the protein coding capability of coronavirus defective viral genomes by mass spectrometry.通过质谱法鉴定冠状病毒缺陷病毒基因组的蛋白编码能力。
Virol J. 2023 Dec 7;20(1):290. doi: 10.1186/s12985-023-02252-3.
6
Genomic Epidemiology, Evolution, and Transmission Dynamics of Porcine Deltacoronavirus.猪德尔塔冠状病毒的基因组流行病学、进化和传播动力学。
Mol Biol Evol. 2020 Sep 1;37(9):2641-2654. doi: 10.1093/molbev/msaa117.
7
Molecular Evolution and Structural Mapping of N-Terminal Domain in Spike Gene of Middle East Respiratory Syndrome Coronavirus (MERS-CoV).中东呼吸综合征冠状病毒(MERS-CoV)刺突基因 N 端结构域的分子进化与结构定位。
Viruses. 2020 May 2;12(5):502. doi: 10.3390/v12050502.
8
A Novel Potentially Recombinant Rodent Coronavirus with a Polybasic Cleavage Site in the Spike Protein.一种新型具有多碱性裂解位点的 Spike 蛋白的潜在重组啮齿动物冠状病毒。
J Virol. 2021 Oct 27;95(22):e0117321. doi: 10.1128/JVI.01173-21. Epub 2021 Aug 25.
9
Longitudinal analysis of SARS-CoV-2 spike and RNA-dependent RNA polymerase protein sequences reveals the emergence and geographic distribution of diverse mutations.对 SARS-CoV-2 刺突蛋白和 RNA 依赖性 RNA 聚合酶蛋白序列的纵向分析揭示了多种突变的出现和地理分布。
Infect Genet Evol. 2022 Jan;97:105153. doi: 10.1016/j.meegid.2021.105153. Epub 2021 Nov 18.
10
In-silico nucleotide and protein analyses of S-gene region in selected zoonotic coronaviruses reveal conserved domains and evolutionary emergence with trajectory course of viral entry from SARS-CoV-2 genomic data.对选定的人畜共患冠状病毒 S 基因区域进行的核苷酸和蛋白质计算机分析揭示了保守结构域,并从 SARS-CoV-2 基因组数据中推断出病毒进入的轨迹和进化起源。
Pan Afr Med J. 2020 Nov 30;37:285. doi: 10.11604/pamj.2020.37.285.24663. eCollection 2020.

引用本文的文献

1
Diverse effects of coronavirus-defective viral genomes on the synthesis of IFNβ and ISG15 mRNAs and coronavirus replication.冠状病毒缺陷病毒基因组对IFNβ和ISG15 mRNA合成及冠状病毒复制的多样影响。
Virol J. 2025 Feb 14;22(1):37. doi: 10.1186/s12985-025-02654-5.
2
Accumulation Dynamics of Defective Genomes during Experimental Evolution of Two Betacoronaviruses.两种β冠状病毒实验进化过程中缺陷基因组的积累动态
Viruses. 2024 Apr 20;16(4):644. doi: 10.3390/v16040644.

本文引用的文献

1
SARS-CoV-2 variant biology: immune escape, transmission and fitness.SARS-CoV-2 变体生物学:免疫逃逸、传播和适应性。
Nat Rev Microbiol. 2023 Mar;21(3):162-177. doi: 10.1038/s41579-022-00841-7. Epub 2023 Jan 18.
2
Spike and nsp6 are key determinants of SARS-CoV-2 Omicron BA.1 attenuation.刺突蛋白和非结构蛋白6是新冠病毒奥密克戎BA.1毒株致病性减弱的关键决定因素。
Nature. 2023 Mar;615(7950):143-150. doi: 10.1038/s41586-023-05697-2. Epub 2023 Jan 11.
3
Remdesivir-induced emergence of SARS-CoV2 variants in patients with prolonged infection.
瑞德西韦在延长感染患者体内诱导出现 SARS-CoV2 变异株。
Cell Rep Med. 2022 Sep 20;3(9):100735. doi: 10.1016/j.xcrm.2022.100735. Epub 2022 Aug 16.
4
Pango lineage designation and assignment using SARS-CoV-2 spike gene nucleotide sequences.使用 SARS-CoV-2 刺突基因核苷酸序列对 Pango 谱系进行指定和分配。
BMC Genomics. 2022 Feb 11;23(1):121. doi: 10.1186/s12864-022-08358-2.
5
In vitro selection of Remdesivir resistance suggests evolutionary predictability of SARS-CoV-2.在体外筛选瑞德西韦耐药性表明了 SARS-CoV-2 的进化可预测性。
PLoS Pathog. 2021 Sep 17;17(9):e1009929. doi: 10.1371/journal.ppat.1009929. eCollection 2021 Sep.
6
Increased transmissibility and global spread of SARS-CoV-2 variants of concern as at June 2021.截至2021年6月,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变异株的传播性增加及其在全球的传播情况。
Euro Surveill. 2021 Jun;26(24). doi: 10.2807/1560-7917.ES.2021.26.24.2100509.
7
SARS-CoV-2 spike protein interacts with and activates TLR41.严重急性呼吸综合征冠状病毒2刺突蛋白与Toll样受体4相互作用并激活它。
Cell Res. 2021 Jul;31(7):818-820. doi: 10.1038/s41422-021-00495-9. Epub 2021 Mar 19.
8
Quasispecies Theory in Virology.病毒学中的准种理论
J Virol. 2002 Jan 1;76(1):463-465. doi: 10.1128/JVI.76.1.463-465.2002.
9
Coronavirus biology and replication: implications for SARS-CoV-2.冠状病毒的生物学与复制:对 SARS-CoV-2 的启示。
Nat Rev Microbiol. 2021 Mar;19(3):155-170. doi: 10.1038/s41579-020-00468-6. Epub 2020 Oct 28.
10
Effects of Coronavirus Persistence on the Genome Structure and Subsequent Gene Expression, Pathogenicity and Adaptation Capability.冠状病毒持续存在对基因组结构和随后的基因表达、致病性和适应能力的影响。
Cells. 2020 Oct 19;9(10):2322. doi: 10.3390/cells9102322.