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. 2021 Oct 13;4:1196. doi: 10.1038/s42003-021-02728-4

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — The most representative amino acid mutations of each variant were selected to construct pseudotyped virus for this study. Each mutation in each SARS-CoV-2 variant is indicated relative to the reference D614G sequence. A dot indicates an identical amino acid at the indicated position, while a dash indicates a deletion at that point. SP sigmal peptide, TM transmembrane domain, RBD Receptor-binding domain.