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在法国南部的三例聚集性病例中培养并鉴定出一种“德尔塔-奥密克戎” SARS-CoV-2。

Culture and identification of a "Deltamicron" SARS-CoV-2 in a three cases cluster in southern France.

机构信息

IHU Méditerranée Infection, Marseille, France.

Aix-Marseille Univ., Institut de Recherche pour le Développement (IRD), Microbes Evolution Phylogeny and Infections (MEPHI), Marseille, France.

出版信息

J Med Virol. 2022 Aug;94(8):3739-3749. doi: 10.1002/jmv.27789. Epub 2022 May 6.

Abstract

Multiple SARS-CoV-2 variants have successively, or concomitantly spread worldwide since the summer of 2020. A few co-infections with different variants were reported and genetic recombinations, common among coronaviruses, were reported or suspected based on co-detection of signature mutations of different variants in a given genome. Here we report three infections in southern France with a Delta 21J_AY.4-Omicron 21K/BA.1 "Deltamicron" recombinant. The hybrid genome harbors signature mutations of the two lineages, supported by a mean sequencing depth of 1163-1421 reads and a mean nucleotide diversity of 0.1%-0.6%. It is composed of the near full-length spike gene (from codons 156-179) of an Omicron 21K/BA.1 variant in a Delta 21J/AY.4 lineage backbone. Importantly, we cultured an isolate of this recombinant and sequenced its genome. It was observed by scanning electron microscopy. As it is misidentified with current variant screening quantitative polymerase chain reaction (qPCR), we designed and implemented for routine diagnosis a specific duplex qPCR. Finally, structural analysis of the recombinant spike suggested its hybrid content could optimize viral binding to the host cell membrane. These findings prompt further studies of the virological, epidemiological, and clinical features of this recombinant.

摘要

自 2020 年夏天以来,多种 SARS-CoV-2 变异株相继或同时在全球范围内传播。据报道,有少数几种不同变异株的合并感染病例,并且根据在给定基因组中同时检测到不同变异株的特征突变,报告或怀疑存在冠状病毒中的基因重组。在这里,我们报告了法国南部的三例感染,涉及 Delta 21J_AY.4-Omicron 21K/BA.1“Deltamicron”重组病毒。杂交基因组携带有这两个谱系的特征突变,这得到了平均测序深度为 1163-1421 个读数和平均核苷酸多样性为 0.1%-0.6%的支持。它由一个 Omicron 21K/BA.1 变体的全长近 Spike 基因(从密码子 156-179)组成,位于 Delta 21J/AY.4 谱系的主干上。重要的是,我们培养了该重组病毒的一个分离株并对其基因组进行了测序。它通过扫描电子显微镜观察到。由于它与当前的变异株筛选定量聚合酶链反应(qPCR)错误识别,因此我们设计并实施了一种用于常规诊断的特异性双重 qPCR。最后,对重组 Spike 的结构分析表明,其杂交内容可以优化病毒与宿主细胞膜的结合。这些发现促使对该重组病毒的病毒学、流行病学和临床特征进行进一步研究。

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