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亚美尼亚的 SARS-CoV-2 谱系的分子分析。

Molecular Analysis of SARS-CoV-2 Lineages in Armenia.

机构信息

Laboratory of Human Genomics, Institute of Molecular Biology NAS RA, Yerevan 0014, Armenia.

Institute of Biomedicine and Pharmacy, Russian-Armenian University, Yerevan 0051, Armenia.

出版信息

Viruses. 2022 May 17;14(5):1074. doi: 10.3390/v14051074.

DOI:10.3390/v14051074
PMID:35632815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9142918/
Abstract

The sequencing of SARS-CoV-2 provides essential information on viral evolution, transmission, and epidemiology. In this paper, we performed the whole-genome sequencing of SARS-CoV-2 using nanopore and Illumina sequencing to describe the circulation of the virus lineages in Armenia. The analysis of 145 full genomes identified six clades (19A, 20A, 20B, 20I, 21J, and 21K) and considerable intra-clade PANGO lineage diversity. Phylodynamic and transmission analysis allowed to attribute specific clades as well as infer their importation routes. Thus, the first two waves of positive case increase were caused by the 20B clade, the third peak caused by the 20I (Alpha), while the last two peaks were caused by the 21J (Delta) and 21K (Omicron) variants. The functional analyses of mutations in sequences largely affected epitopes associated with protective HLA loci and did not cause the loss of the signal in PCR tests targeting ORF1ab and N genes as confirmed by RT-PCR. We also compared the performance of nanopore and Illumina short-read sequencing and showed the utility of nanopore sequencing as an efficient and affordable alternative for large-scale molecular epidemiology research. Thus, our paper describes new data on the genomic diversity of SARS-CoV-2 variants in Armenia in the global context of the virus molecular genomic surveillance.

摘要

对 SARS-CoV-2 的测序提供了关于病毒进化、传播和流行病学的重要信息。在本文中,我们使用纳米孔和 Illumina 测序对 SARS-CoV-2 进行了全基因组测序,以描述病毒谱系在亚美尼亚的传播情况。对 145 个全基因组的分析确定了六个分支(19A、20A、20B、20I、21J 和 21K)和相当大的分支内 PANGO 谱系多样性。系统发育和传播分析可以确定特定的分支,并推断它们的传入途径。因此,前两波阳性病例的增加是由 20B 分支引起的,第三波是由 20I(Alpha)引起的,而最后两波是由 21J(Delta)和 21K(Omicron)变体引起的。序列中突变的功能分析在很大程度上影响了与保护性 HLA 位点相关的表位,并且没有导致针对 ORF1ab 和 N 基因的 PCR 测试的信号丢失,这一点通过 RT-PCR 得到了证实。我们还比较了纳米孔和 Illumina 短读测序的性能,并展示了纳米孔测序作为大规模分子流行病学研究的高效且经济实惠的替代方法的实用性。因此,我们的论文在病毒分子基因组监测的全球背景下,描述了亚美尼亚 SARS-CoV-2 变体基因组多样性的新数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/32f0a040b741/viruses-14-01074-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/8dcbca5d6924/viruses-14-01074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/1c682174e9e5/viruses-14-01074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/7199877cc127/viruses-14-01074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/b44e071cdc43/viruses-14-01074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/32f0a040b741/viruses-14-01074-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/8dcbca5d6924/viruses-14-01074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/1c682174e9e5/viruses-14-01074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/7199877cc127/viruses-14-01074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/b44e071cdc43/viruses-14-01074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc67/9142918/32f0a040b741/viruses-14-01074-g005.jpg

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