Sanderson Theo, Barrett Jeffrey C
Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
Francis Crick Institute, London, NW1 1AT, UK.
Wellcome Open Res. 2021 Nov 10;6:305. doi: 10.12688/wellcomeopenres.17295.1. eCollection 2021.
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.
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。