Generation of false-positive SARS-CoV-2 antigen results with testing conditions outside manufacturer recommendations: A scientific approach to pandemic misinformation

Glenn Patriquin, Ross J. Davidson, Todd F. Hatchette, Breanne M. Head, Edgard Mejia, Michael G. Becker, Adrienne Meyers, Paul Sandstrom, Jacob Hatchette, Ava Block, Nicole Smith, John Ross, Jason J. LeBlanc

Résultat de recherche: Articleexamen par les pairs

30 Citations (Scopus)

Résumé

Antigen-based rapid diagnostics tests (Ag-RDTs) are useful tools for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection. However, misleading demonstrations of the Abbott Panbio coronavirus disease 2019 (COVID- 19) Ag-RDT on social media claimed that SARS-CoV-2 antigen could be detected in municipal water and food products. To offer a scientific rebuttal to pandemic misinformation and disinformation, this study explored the impact of using the Panbio SARS-CoV-2 assay with conditions falling outside manufacturer recommendations. Using Panbio, various water and food products, laboratory buffers, and SARS-CoV-2- negative clinical specimens were tested with and without manufacturer buffer. Additional experiments were conducted to assess the role of each Panbio buffer component (tricine, NaCl, pH, and Tween 20) as well as the impact of temperature (4°C, 20°C, and 45°C) and humidity (90%) on assay performance. Direct sample testing (without the kit buffer) resulted in false-positive signals resembling those obtained with SARS-CoV-2 positive controls tested under proper conditions. The likely explanation of these artifacts is nonspecific interactions between the SARSCoV- 2-specific conjugated and capture antibodies, as proteinase K treatment abrogated this phenomenon, and thermal shift assays showed pH-induced conformational changes under conditions promoting artifact formation. Omitting, altering, and reverse engineering the kit buffer all supported the importance of maintaining buffering capacity, ionic strength, and pH for accurate kit function. Interestingly, the Panbio assay could tolerate some extremes of temperature and humidity outside manufacturer claims. Our data support strict adherence to manufacturer instructions to avoid false-positive SARS-CoV-2 Ag-RDT reactions, otherwise resulting in anxiety, overuse of public health resources, and dissemination of misinformation. IMPORTANCE With the Panbio severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen test being deployed in over 120 countries worldwide, understanding conditions required for its ideal performance is critical. Recently on social media, this kit was shown to generate false positives when manufacturer recommendations were not followed. While erroneous results from improper use of a test may not be surprising to some health care professionals, understanding why false positives occur can help reduce the propagation of misinformation and provide a scientific rebuttal for these aberrant findings. This study demonstrated that the kit buffer's pH, ionic strength, and buffering capacity were critical components to ensure proper kit function and avoid generation of false-positive results. Typically, false positives arise from cross-reacting or interfering substances; however, this study demonstrated a mechanism where false positives were generated under conditions favoring nonspecific interactions between the two antibodies designed for SARS-CoV-2 antigen detection. Following the manufacturer instructions is critical for accurate test results.

Langue d'origineEnglish
Numéro d'articlee00683-21
JournalMicrobiology spectrum
Volume9
Numéro de publication2
DOI
Statut de publicationPublished - oct. 2021

Note bibliographique

Funding Information:
This work received no private or public funding, with the exception of the Panbio kits that were provided in-kind from the Public Health Agency of Canada (PHAC). We thank the Special Pathogens Program of the National Microbiology Laboratory (NML) (Winnipeg, Manitoba) for the gamma-irradiated SARS-CoV-2 virus used in this study. We would also like to recognize the ongoing efforts of all the NML and NSH staff for their dedication and exceptional services throughout the pandemic, including the help with RT-PCR testing during this evaluation. We also thank all the volunteers and health care professionals who dedicate their time at popup clinics and other settings that use Ag- RDTs or NAATs. You are all instrumental for our pandemic responses and safety in our communities.

Publisher Copyright:
© Crown copyright 2021.

ASJC Scopus Subject Areas

  • Physiology
  • Ecology
  • General Immunology and Microbiology
  • Genetics
  • Microbiology (medical)
  • Cell Biology
  • Infectious Diseases

PubMed: MeSH publication types

  • Journal Article

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