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使用变异特异性仓鼠血清进行抗原作图显示,奥密克戎亚变体之间存在大量抗原变异。

Antigenic cartography using variant-specific hamster sera reveals substantial antigenic variation among Omicron subvariants.

机构信息

Institute of Virology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin 10117, Germany.

German Centre for Infection Research (Deutsches Zentrum für Infektionsforschung), Berlin 10117, Germany.

出版信息

Proc Natl Acad Sci U S A. 2024 Aug 6;121(32):e2310917121. doi: 10.1073/pnas.2310917121. Epub 2024 Jul 30.

DOI:10.1073/pnas.2310917121
PMID:39078681
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11317614/
Abstract

Severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2) has developed substantial antigenic variability. As the majority of the population now has pre-existing immunity due to infection or vaccination, the use of experimentally generated animal immune sera can be valuable for measuring antigenic differences between virus variants. Here, we immunized Syrian hamsters by two successive infections with one of nine SARS-CoV-2 variants. Their sera were titrated against 16 SARS-CoV-2 variants, and the resulting titers were visualized using antigenic cartography. The antigenic map shows a condensed cluster containing all pre-Omicron variants (D614G, Alpha, Delta, Beta, Mu, and an engineered B.1+E484K variant) and considerably more diversity among a selected panel of Omicron subvariants (BA.1, BA.2, BA.4/BA.5, the BA.5 descendants BF.7 and BQ.1.18, the BA.2.75 descendant BN.1.3.1, the BA.2-derived recombinants XBB.2 and EG.5.1, and the BA.2.86 descendant JN.1). Some Omicron subvariants were as antigenically distinct from each other as the wildtype is from the Omicron BA.1 variant. Compared to titers measured in human sera, titers in hamster sera are of higher magnitude, show less fold change, and result in a more compact antigenic map topology. The results highlight the potential of sera from hamsters for the continued antigenic characterization of SARS-CoV-2.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)已经产生了大量的抗原变异性。由于大多数人现在因感染或接种疫苗而具有预先存在的免疫力,因此使用实验生成的动物免疫血清可用于测量病毒变异体之间的抗原差异。在这里,我们通过连续两次用九种 SARS-CoV-2 变体之一感染叙利亚仓鼠来免疫它们。他们的血清针对 16 种 SARS-CoV-2 变体进行滴定,并使用抗原图谱可视化得到的滴度。抗原图谱显示一个包含所有前奥密克戎变体(D614G、Alpha、Delta、Beta、Mu 和一种工程化的 B.1+E484K 变体)的浓缩簇,并且在奥密克戎亚变体(BA.1、BA.2、BA.4/BA.5、BA.5 后代 BF.7 和 BQ.1.18、BA.2.75 后代 BN.1.3.1、BA.2 衍生的重组体 XBB.2 和 EG.5.1 以及 BA.2.86 后代 JN.1)的选定面板中存在更多的多样性。一些奥密克戎亚变体彼此之间的抗原差异与野生型与奥密克戎 BA.1 变体之间的差异一样大。与在人血清中测量的滴度相比,仓鼠血清中的滴度幅度更高,折叠变化更小,并且产生更紧凑的抗原图谱拓扑结构。这些结果突出了仓鼠血清在 SARS-CoV-2 持续抗原特征分析方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd21/11317614/6161c3e7531e/pnas.2310917121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd21/11317614/afdf56c03bc2/pnas.2310917121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd21/11317614/4ebabedda1e6/pnas.2310917121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd21/11317614/6161c3e7531e/pnas.2310917121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd21/11317614/afdf56c03bc2/pnas.2310917121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd21/11317614/4ebabedda1e6/pnas.2310917121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd21/11317614/6161c3e7531e/pnas.2310917121fig03.jpg

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