School of Chemistry and Molecular Biosciences, University of Queensland, St. Lucia, QLD, Australia.
Australian Institute for Biotechnology and Nanotechnology, University of Queensland, St. Lucia, QLD, Australia.
Front Immunol. 2022 Jun 10;13:926262. doi: 10.3389/fimmu.2022.926262. eCollection 2022.
Since the start of the COVID-19 pandemic, multiple waves of SARS-CoV-2 variants have emerged. Of particular concern is the omicron variant, which harbors 28 mutations in the spike glycoprotein receptor binding and N-terminal domains relative to the ancestral strain. The high mutability of SARS-CoV-2 therefore poses significant hurdles for development of universal assays that rely on spike-specific immune detection. To address this, more conserved viral antigens need to be targeted. In this work, we comprehensively demonstrate the use of nucleocapsid (N)-specific detection across several assays using previously described nanobodies C2 and E2. We show that these nanobodies are highly sensitive and can detect divergent SARS-CoV-2 ancestral, delta and omicron variants across several assays. By comparison, spike-specific antibodies S309 and CR3022 only disparately detect SARS-CoV-2 variant targets. As such, we conclude that N-specific detection could provide a standardized universal target for detection of current and emerging SARS-CoV-2 variants of concern.
自 COVID-19 大流行开始以来,已经出现了多波 SARS-CoV-2 变体。特别值得关注的是奥密克戎变体,它相对于原始毒株在刺突糖蛋白受体结合和 N 端结构域中具有 28 个突变。因此,SARS-CoV-2 的高变异性给依赖刺突特异性免疫检测的通用检测方法的开发带来了重大障碍。为了解决这个问题,需要针对更保守的病毒抗原。在这项工作中,我们使用先前描述的纳米抗体 C2 和 E2 在几种检测方法中全面证明了核衣壳 (N)-特异性检测的用途。我们表明,这些纳米抗体具有高度的敏感性,可以在几种检测方法中检测到不同的 SARS-CoV-2 原始、德尔塔和奥密克戎变体。相比之下,刺突特异性抗体 S309 和 CR3022 仅离散地检测 SARS-CoV-2 变体靶标。因此,我们得出结论,N-特异性检测可以为当前和新出现的 SARS-CoV-2 变体提供标准化的通用检测目标。