Suppr超能文献

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)德尔塔基因组中刺突蛋白第142位的变异是由测序扩增子缺失导致的技术假象。

Variation at Spike position 142 in SARS-CoV-2 Delta genomes is a technical artifact caused by dropout of a sequencing amplicon.

作者信息

Sanderson Theo, Barrett Jeffrey C

机构信息

Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.

Francis Crick Institute, London, NW1 1AT, UK.

出版信息

Wellcome Open Res. 2021 Nov 10;6:305. doi: 10.12688/wellcomeopenres.17295.1. eCollection 2021.

Abstract

Public SARS-CoV-2 genomes from the Delta lineage show complex and confusing patterns of mutations at Spike codon 142, and at another nearby position, Spike codon 95. It has been hypothesised that these represent recurrent mutations with interesting evolutionary dynamics, and that these mutations may affect viral load. Here we show that these patterns, and the relationship with viral load, are artifacts of sequencing difficulties in this region of the Delta genome caused be a deletion in the binding site for the 72_RIGHT primer of the ARTIC V3 schema. Spike G142D should be considered a lineage-defining mutation of Delta.

摘要

来自德尔塔谱系的新冠病毒公共基因组在刺突蛋白密码子142以及附近另一个位置——刺突蛋白密码子95处,呈现出复杂且令人困惑的突变模式。据推测,这些代表了具有有趣进化动态的反复突变,并且这些突变可能会影响病毒载量。在此我们表明,这些模式以及与病毒载量的关系,是由ARTIC V3方案中72_RIGHT引物结合位点的缺失导致的德尔塔基因组该区域测序困难所造成的假象。刺突蛋白G142D应被视为德尔塔谱系定义性突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74eb/9117943/c5e0b57506d2/wellcomeopenres-6-19122-g0000.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