IHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005, Marseille, France.
Microbes Evolution Phylogeny and Infections (MEPHI), Institut de Recherche Pour Le Développement (IRD), Assistance Publique-Hôpitaux de Marseille (AP-HM), MEPHI, Aix-Marseille Univ., 27 Boulevard Jean Moulin, 13005, Marseille, France.
Sci Rep. 2022 Nov 4;12(1):18721. doi: 10.1038/s41598-022-22060-z.
At the time of a new and unprecedented viral pandemic, many questions are being asked about the genomic evolution of SARS-CoV-2 and the emergence of different variants, leading to therapeutic and immune evasion and survival of this genetically highly labile RNA virus. The nasopharyngeal persistence of infectious virus beyond 17 days proves its constant interaction with the human immune system and increases the intra-individual mutational possibilities. We performed a prospective high-throughput sequencing study (ARTIC Nanopore) of SARS-CoV-2 from so-called "persistent" patients, comparing them with a non-persistent population, and analyzing the quasi-species present in a single sample at time t. Global intra-individual variability in persistent patients was found to be higher than in controls (mean 5.3%, Standard deviation 0.9 versus 4.6% SD 0.3, respectively, p < 0.001). In the detailed analysis, we found a greater difference between persistent and non-persistent patients with non-severe COVID 19, and between the two groups infected with clade 20A. Furthermore, we found minority N501Y and P681H mutation clouds in all patients, with no significant differences found both groups. The question of the SARS-CoV-2 viral variants' genesis remains to be further investigated, with the need to prevent new viral propagations and their consequences, and quasi-species analysis could be an important key to watch out.
在新的、前所未有的病毒大流行时期,人们对 SARS-CoV-2 的基因组进化以及不同变体的出现提出了许多问题,这些变体导致了治疗和免疫逃逸,以及这种遗传上高度不稳定的 RNA 病毒的存活。传染性病毒在鼻咽部持续存在超过 17 天,证明了它与人体免疫系统的持续相互作用,并增加了个体内突变的可能性。我们对所谓的“持续性”患者进行了 SARS-CoV-2 的前瞻性高通量测序研究(ARTIC Nanopore),将其与非持续性人群进行了比较,并分析了单个样本在 t 时存在的准种。我们发现,持续性患者的个体内全球变异性高于对照组(分别为 5.3%,标准差 0.9 与 4.6%,标准差 0.3,p<0.001)。在详细分析中,我们发现非严重 COVID-19 的持续性和非持续性患者之间存在更大差异,并且在感染 20A 谱系的两组患者之间也存在更大差异。此外,我们在所有患者中均发现了少数 N501Y 和 P681H 突变云,但两组之间均未发现显著差异。SARS-CoV-2 病毒变体的起源问题仍有待进一步研究,需要防止新的病毒传播及其后果,而准种分析可能是一个值得关注的重要关键。