Frontiers in Immunology (Jun 2022)

Nucleocapsid Specific Diagnostics for the Detection of Divergent SARS-CoV-2 Variants

  • Ariel Isaacs,
  • Alberto A. Amarilla,
  • Julio Aguado,
  • Naphak Modhiran,
  • Eduardo A. Albornoz,
  • Alireza A. Baradar,
  • Christopher L. D. McMillan,
  • Jovin J. Y. Choo,
  • Adi Idris,
  • Aroon Supramaniam,
  • Nigel A. J. McMillan,
  • David A. Muller,
  • David A. Muller,
  • Paul R. Young,
  • Paul R. Young,
  • Trent M. Woodruff,
  • Ernst J. Wolvetang,
  • Keith J. Chappell,
  • Keith J. Chappell,
  • Keith J. Chappell,
  • Daniel Watterson,
  • Daniel Watterson,
  • Daniel Watterson

DOI
https://doi.org/10.3389/fimmu.2022.926262
Journal volume & issue
Vol. 13

Abstract

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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.

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