Department of Molecular and Translational Medicine, Section of Microbiology, University of Brescia, Brescia, Italy.
Instituto Rene Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Minas Gerais, Brazil.
J Med Virol. 2023 Jun;95(6):e28848. doi: 10.1002/jmv.28848.
During COVID-19 pandemic, consensus genomic sequences were used for rapidly monitor the spread of the virus worldwide. However, less attention was paid to intrahost genetic diversity. In fact, in the infected host, SARS-CoV-2 consists in an ensemble of replicating and closely related viral variants so-called quasispecies. Here we show that intrahost single nucleotide variants (iSNVs) represent a target for contact tracing analysis. Our data indicate that in the acute phase of infection, in highly likely transmission links, the number of viral particles transmitted from one host to another (bottleneck size) is large enough to propagate iSNVs among individuals. Furthermore, we demonstrate that, during SARS-CoV-2 outbreaks when the consensus sequences are identical, it is possible to reconstruct the transmission chains by genomic investigations of iSNVs. Specifically, we found that it is possible to identify transmission chains by limiting the analysis of iSNVs to only three well-conserved genes, namely nsp2, ORF3, and ORF7.
在 COVID-19 大流行期间,共识基因组序列被用于快速监测病毒在全球范围内的传播。然而,人们对宿主内遗传多样性的关注较少。事实上,在感染宿主中,SARS-CoV-2 由一组复制和密切相关的病毒变体组成,即准种。在这里,我们表明宿主内单核苷酸变异(iSNVs)是接触追踪分析的一个目标。我们的数据表明,在感染的急性期,在高度可能的传播联系中,从一个宿主传播到另一个宿主的病毒颗粒数量(瓶颈大小)足够大,可以在个体之间传播 iSNVs。此外,我们证明,在共识序列相同时爆发 SARS-CoV-2 时,可以通过对 iSNVs 的基因组研究来重建传播链。具体来说,我们发现通过将 iSNVs 的分析仅限于三个保守性较好的基因(nsp2、ORF3 和 ORF7),就有可能识别传播链。