A straightforward molecular strategy to retrospectively investigate the spread of SARS-CoV-2 VOC202012/01 B.1.1.7 variant

被引:10
作者
Ibba, Gabriele [1 ,2 ]
Sau, Rosangela [1 ]
Angioj, Flavia [2 ]
Abbondio, Marcello [1 ]
Rubino, Salvatore [1 ,2 ]
Uzzau, Sergio [1 ,2 ]
机构
[1] Univ Sassari, Div Microbiol & Virol, Dept Biomed Sci, I-07100 Sassari, Italy
[2] Azienda Osped Univ, Microbiol & Virol, I-07100 Sassari, Italy
来源
JOURNAL OF INFECTION IN DEVELOPING COUNTRIES | 2021年 / 15卷 / 02期
基金
加拿大健康研究院;
关键词
SARS-CoV-2; B.1.1.7; variant; RT-PCR; molecular diagnostics;
D O I
10.3855/jidc.14972
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The spread of new SARS-CoV-2 variants represents a serious threat worldwide, thus rapid and cost-effective methods are required for their identification. Since November 2020, the TaqPath COVID-19 assay (Thermo Fisher Scientific) has been used to identify viral strains of the new lineage B.1.1.7, since it fails to detect the S-gene with Delta 69/70 deletion. Here, we proposed S-gene mutations screening with the Allplex SARS-CoV-2 assay (Seegene), another widely used RT-PCR test that targets Sarbecovirus E, SARS-CoV-2 N, and RdRp/S genes. Accordingly, we evaluated the S gene amplification curve pattern compared to those of the other genes. Exploiting an Allplex assay-generated dataset, we screened 663 RT-PCR digital records, including all SARS-CoV-2 respiratory samples tested in our laboratory with the Allplex assay between January 1st and February 25th, 2021. This approach enabled us to detect 64 samples with peculiar non-sigmoidal amplification curves. Sequencing a selected group of 4 RNA viral genomes demonstrated that those curves were associated with B.1.1.7 variant strains. Our results strongly suggest that B.1.1.7 variant spread has begun in this area at least since January and imply the potential of these analytical methods to track and characterize the spread of B.1.1.7 strains in those areas where Allplex SARS-CoV-2 datasets have been previously recorded.
引用
收藏
页码:242 / +
页数:6
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