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RNA依赖的RNA聚合酶(RdRp)突变与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)基因组进化相关。

RdRp mutations are associated with SARS-CoV-2 genome evolution.

作者信息

Eskier Doğa, Karakülah Gökhan, Suner Aslı, Oktay Yavuz

机构信息

Izmir Biomedicine and Genome Center (IBG), Izmir, Turkey.

Izmir International Biomedicine and Genome Institute, Dokuz Eylül University, Izmir, Turkey.

出版信息

PeerJ. 2020 Jul 21;8:e9587. doi: 10.7717/peerj.9587. eCollection 2020.

DOI:10.7717/peerj.9587
PMID:32742818
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7380272/
Abstract

COVID-19, caused by the novel SARS-CoV-2 virus, started in China in late 2019, and soon became a global pandemic. With the help of thousands of viral genome sequences that have been accumulating, it has become possible to track the evolution of the viral genome over time as it spread across the world. An important question that still needs to be answered is whether any of the common mutations affect the viral properties, and therefore the disease characteristics. Therefore, we sought to understand the effects of mutations in RNA-dependent RNA polymerase (RdRp), particularly the common 14408C>T mutation, on mutation rate and viral spread. By focusing on mutations in the slowly evolving M or E genes, we aimed to minimize the effects of selective pressure. Our results indicate that 14408C>T mutation increases the mutation rate, while the third-most common RdRp mutation, 15324C>T, has the opposite effect. It is possible that 14408C>T mutation may have contributed to the dominance of its co-mutations in Europe and elsewhere.

摘要

由新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)于2019年末在中国爆发,并迅速演变成一场全球大流行。借助不断积累的数千个病毒基因组序列,追踪病毒基因组在全球传播过程中的随时间演变已成为可能。一个仍有待解答的重要问题是,是否有任何常见突变会影响病毒特性,进而影响疾病特征。因此,我们试图了解RNA依赖性RNA聚合酶(RdRp)中的突变,特别是常见的14408C>T突变,对突变率和病毒传播的影响。通过关注缓慢进化的M或E基因中的突变,我们旨在将选择压力的影响降至最低。我们的结果表明,14408C>T突变会增加突变率,而第三常见的RdRp突变15324C>T则有相反的效果。14408C>T突变可能促成了其共突变在欧洲和其他地区的主导地位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a03/7380272/eeb7314b4d84/peerj-08-9587-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a03/7380272/0db5fc817f72/peerj-08-9587-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a03/7380272/eeb7314b4d84/peerj-08-9587-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a03/7380272/0db5fc817f72/peerj-08-9587-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a03/7380272/eeb7314b4d84/peerj-08-9587-g002.jpg

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本文引用的文献

1
The protein expression profile of ACE2 in human tissues.ACE2 在人体组织中的蛋白表达谱。
Mol Syst Biol. 2020 Jul;16(7):e9610. doi: 10.15252/msb.20209610.
2
Potential implications of novel coronavirus disease (COVID-19) related gastrointestinal symptoms for abdominal imaging.新型冠状病毒肺炎(COVID-19)相关胃肠道症状对腹部影像学检查的潜在影响
Radiography (Lond). 2020 Aug;26(3):274. doi: 10.1016/j.radi.2020.04.016. Epub 2020 May 1.
3
Emerging Evidence for Neuropsycho-Consequences of COVID-19.COVID-19 相关神经精神后果的新证据。
基因特异性ω的渐进进化动力学导致具有超级感染力和毒力的新型 SARS-CoV-2 菌株的出现,这些菌株具有疫苗中和作用。
Int J Mol Sci. 2024 Jun 7;25(12):6306. doi: 10.3390/ijms25126306.
4
The RdRp genotyping of SARS-CoV-2 isolated from patients with different clinical spectrum of COVID-19.从不同临床谱 COVID-19 患者中分离的 SARS-CoV-2 的 RdRp 基因分型。
BMC Infect Dis. 2024 Mar 4;24(1):281. doi: 10.1186/s12879-024-09146-x.
5
Sequence analysis of the Spike, RNA-dependent RNA polymerase, and protease genes reveals a distinct evolutionary pattern of SARS-CoV-2 variants circulating in Yogyakarta and Central Java provinces, Indonesia.对 Spike、RNA 依赖性 RNA 聚合酶和蛋白酶基因进行序列分析,揭示了印度尼西亚日惹特区和中爪哇省流行的 SARS-CoV-2 变异株的独特进化模式。
Virus Genes. 2024 Apr;60(2):105-116. doi: 10.1007/s11262-023-02048-1. Epub 2024 Jan 20.
6
Sequence Analysis of Hot Spot Regions of Spike and RNA-dependent-RNA polymerase (RdRp) Genes of SARS-CoV-2 in Kerman, Iran.伊朗克尔曼2019冠状病毒病刺突蛋白和RNA依赖性RNA聚合酶(RdRp)基因热点区域的序列分析
Mediterr J Hematol Infect Dis. 2023 Jul 1;15(1):e2023042. doi: 10.4084/MJHID.2023.042. eCollection 2023.
7
Molecular Epidemiology of SARS-CoV-2 during Five COVID-19 Waves and the Significance of Low-Frequency Lineages.SARS-CoV-2 的分子流行病学在五次 COVID-19 浪潮期间以及低频谱系的意义。
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8
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Inform Med Unlocked. 2023;39:101256. doi: 10.1016/j.imu.2023.101256. Epub 2023 Apr 25.
9
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J Clin Med. 2023 Mar 19;12(6):2371. doi: 10.3390/jcm12062371.
10
Genomic Surveillance of SARS-CoV-2 in the Southern Province of Zambia: Detection and Characterization of Alpha, Beta, Delta, and Omicron Variants of Concern.赞比亚南部省份 SARS-CoV-2 的基因组监测:关注的 Alpha、Beta、Delta 和奥密克戎变异株的检测和特征分析。
Viruses. 2022 Aug 24;14(9):1865. doi: 10.3390/v14091865.
Curr Neuropharmacol. 2021;19(1):92-96. doi: 10.2174/1570159X18666200507085335.
4
Codon Usage and Phenotypic Divergences of SARS-CoV-2 Genes.SARS-CoV-2 基因的密码子使用和表型差异。
Viruses. 2020 Apr 30;12(5):498. doi: 10.3390/v12050498.
5
Genotyping coronavirus SARS-CoV-2: methods and implications.冠状病毒 SARS-CoV-2 的基因分型:方法与意义。
Genomics. 2020 Sep;112(5):3588-3596. doi: 10.1016/j.ygeno.2020.04.016. Epub 2020 Apr 27.
6
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J Transl Med. 2020 Apr 22;18(1):179. doi: 10.1186/s12967-020-02344-6.
7
A Genomic Perspective on the Origin and Emergence of SARS-CoV-2.从基因组角度看 SARS-CoV-2 的起源与出现。
Cell. 2020 Apr 16;181(2):223-227. doi: 10.1016/j.cell.2020.03.035. Epub 2020 Mar 26.
8
Potent binding of 2019 novel coronavirus spike protein by a SARS coronavirus-specific human monoclonal antibody.一种严重急性呼吸系统综合征冠状病毒特异性人源单克隆抗体对 2019 新型冠状病毒刺突蛋白的有效结合。
Emerg Microbes Infect. 2020 Feb 17;9(1):382-385. doi: 10.1080/22221751.2020.1729069. eCollection 2020.
9
Pattern of early human-to-human transmission of Wuhan 2019 novel coronavirus (2019-nCoV), December 2019 to January 2020.2019 年 12 月至 2020 年 1 月期间武汉 2019 年新型冠状病毒(2019-nCoV)人传人模式。
Euro Surveill. 2020 Jan;25(4). doi: 10.2807/1560-7917.ES.2020.25.4.2000058.
10
A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster.一个涉及 2019 年新型冠状病毒的家庭聚集性肺炎病例,提示存在人际传播:一项家庭聚集性研究。
Lancet. 2020 Feb 15;395(10223):514-523. doi: 10.1016/S0140-6736(20)30154-9. Epub 2020 Jan 24.