iScience (Mar 2022)

Assessment of the Abbott BinaxNOW SARS-CoV-2 rapid antigen test against viral variants of concern

  • Anuradha Rao,
  • Leda Bassit,
  • Jessica Lin,
  • Kiran Verma,
  • Heather B. Bowers,
  • Kimberly Pachura,
  • Morgan Greenleaf,
  • Julie Sullivan,
  • Eric Lai,
  • Richard S. Creager,
  • Thomas Pribyl,
  • John Blackwood,
  • Anne L. Piantadosi,
  • Raymond Schinazi,
  • Greg S. Martin,
  • Wilbur A. Lam

Journal volume & issue
Vol. 25, no. 3
p. 103968

Abstract

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Summary: As the emergence of SARS-CoV-2 variants brings the global pandemic to new levels, the performance of current rapid antigen tests against variants of concern and interest (VOC/I) is of significant public health concern. Here, we report assessment of the Abbot BinaxNOW COVID-19 Antigen Self-Test. Using genetically sequenced remnant clinical samples collected from individuals positive for SARS-CoV-2, we assessed the performance of BinaxNOW against the variants that currently pose public health threats. We measured the limit of detection of BinaxNOW against various VOC/I in a blinded manner. BinaxNOW successfully detected the Omicron (B.1.1.529), Mu (B.1.621), Delta (B.1.617.2), Lambda (C.37), Gamma (P.1), Alpha (B.1.1.7), Beta (B.1.351), Eta (B.1.525), and P.2 variants and at low viral concentrations. BinaxNOW also detected the Omicron variant in individual remnant clinical samples. Overall, these data indicate that this inexpensive and simple-to-use, FDA-authorized and broadly distributed rapid test can reliably detect Omicron, Delta, and other VOC/I.

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