Suppr超能文献

全基因组分析揭示了 SARS-CoV-2 病毒密码子使用模式的全球异质性,表明 COVID-19 具有全球差异性。

Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19.

机构信息

Henan International Joint Laboratory for Nuclear Protein Regulation, School of Basic Medical Sciences, Henan University, Kaifeng 475004, Henan, China.

School of Life Sciences, Henan University, Kaifeng 475004, Henan, China.

出版信息

Biomolecules. 2021 Jun 18;11(6):912. doi: 10.3390/biom11060912.

Abstract

The ongoing outbreak of coronavirus disease COVID-19 is significantly implicated by global heterogeneity in the genome organization of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The causative agents of global heterogeneity in the whole genome of SARS-CoV-2 are not well characterized due to the lack of comparative study of a large enough sample size from around the globe to reduce the standard deviation to the acceptable margin of error. To better understand the SARS-CoV-2 genome architecture, we have performed a comprehensive analysis of codon usage bias of sixty (60) strains to get a snapshot of its global heterogeneity. Our study shows a relatively low codon usage bias in the SARS-CoV-2 viral genome globally, with nearly all the over-preferred codons' A.U. ended. We concluded that the SARS-CoV-2 genome is primarily shaped by mutation pressure; however, marginal selection pressure cannot be overlooked. Within the A/U rich virus genomes of SARS-CoV-2, the standard deviation in G.C. (42.91% ± 5.84%) and the GC3 value (30.14% ± 6.93%) points towards global heterogeneity of the virus. Several SARS-CoV-2 viral strains were originated from different viral lineages at the exact geographic location also supports this fact. Taking all together, these findings suggest that the general root ancestry of the global genomes are different with different genome's level adaptation to host. This research may provide new insights into the codon patterns, host adaptation, and global heterogeneity of SARS-CoV-2.

摘要

持续爆发的冠状病毒病 COVID-19 与严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)基因组组织的全球异质性有明显的关联。由于缺乏对来自全球各地足够大的样本量进行比较研究,以将标准差降低到可接受的误差范围内,因此全球 SARS-CoV-2 全基因组的变因尚未得到很好的描述。为了更好地了解 SARS-CoV-2 基因组结构,我们对六十(60)株病毒的密码子使用偏性进行了全面分析,以了解其全球异质性。我们的研究表明,SARS-CoV-2 病毒基因组的密码子使用偏性相对较低,几乎所有过度偏好的密码子的 A.U. 都已结束。我们得出的结论是,SARS-CoV-2 基因组主要受突变压力的影响;但是,不能忽视微小的选择压力。在 SARS-CoV-2 的 A/U 丰富病毒基因组中,G.C. 的标准差(42.91% ± 5.84%)和 GC3 值(30.14% ± 6.93%)表明了病毒的全球异质性。来自不同病毒谱系的几种 SARS-CoV-2 病毒株起源于同一地理位置,也证实了这一事实。总的来说,这些发现表明,全球基因组的一般根源不同,不同的基因组对宿主的适应程度也不同。这项研究可能为 SARS-CoV-2 的密码子模式、宿主适应性和全球异质性提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/102d/8233742/e86622e51241/biomolecules-11-00912-g001.jpg

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