Development and Clinical Performance of InteliSwab® COVID-19 Rapid Test: Evaluation of Antigen Test for the Diagnosis of SARS-CoV-2 and Analytical Sensitivity to Detect Variants of Concern Including Omicron and Subvariants

Author:

Fischl Mark J.1,Young Janean1,Kardos Keith1,Roehler Michele1,Miller Tiffany1,Wooten Melinda1,Holmes Natalie1,Gula Nicole1,Baglivo Mia1,Steen Justin1,Zelenz Nori1,Joyee Antony George1,Munster Vincent2ORCID,Weishampel Zack2,Yinda Claude Kwe2,Rouse Kevin G.3,Gvozden Cathy4,Wever David5,Yanez Giralt6,Anderson Marc7,Yu Song8,Bearie Brian9,Young Stephen10,Berry Jody D.1

Affiliation:

1. OraSure Technologies, Inc., 220 East First St., Bethlehem, PA 18015, USA

2. Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, Hamilton, MT 59840, USA

3. The Children’s Clinic, Jonesboro, AR 72401, USA

4. Gvozden Pediatrics, Millersville, MD 21108, USA

5. Cahaba Research Inc., Pelham, AL 35124, USA

6. South Florida Research Organization, Medley, FL 33166, USA

7. Tanner Clinic, Layton, UT 84041, USA

8. Cahaba Research Inc., MedHelp Urgent Care, Birmingham, AL 32535, USA

9. Urgent Care of Colton, Benchmark Research Group, Colton, CA 92324, USA

10. TriCore Reference Laboratories, Albuquerque, NM 87102, USA

Abstract

Background and objectives: Timely detection of SARS-CoV-2 infection with subsequent contact tracing and rapid isolation are considered critical to containing the pandemic, which continues with the emergence of new variants. Hence, there is an ongoing need for reliable point-of-care antigen rapid diagnostic tests (Ag-RDT). This report describes the development, evaluation, and analytical sensitivity of the diagnostic performance of the InteliSwab® COVID-19 Rapid Test. Methods: Samples from 165 symptomatic subjects were tested with InteliSwab® and the results were compared to RT-PCR to determine the antigen test performance. The analytical sensitivity of InteliSwab® for the detection of different variants was assessed by limit of detection (LOD) determination using recombinant nucleocapsid proteins (NPs) and testing with virus isolates. Western immunoblot independently confirmed that each monoclonal Ab is capable of binding to all variants tested thus far. Results: The overall positivity rate by RT-PCR was 37% for the 165 symptomatic subjects. Based on RT-PCR results as the reference standard, InteliSwab® showed clinical sensitivity and specificity of 85.2% (95% CI, 74.3–92.0%) and 98.1% (95% CI, 93.3–99.7%), respectively. The overall agreement was 93.3% (Kappa index value 0.85; 95% CI, 0.77–0.74) between RT-PCR and InteliSwab® test results. Furthermore, the evaluation of analytical sensitivity for different SARS-CoV-2 variants by InteliSwab® was comparable in the detection of all the variants tested, including Omicron subvariants, BA.4, BA.5, and BQ.1. Conclusions: Due to the surge of infections caused by different variants from time to time, there is a critical need to evaluate the sensitivity of rapid antigen-detecting tests for new variants. The study findings showed the robust diagnostic performance of InteliSwab® and analytical sensitivity in detecting different SARS-CoV-2 variants, including the Omicron subvariants. With the integrated swab and excellent sensitivity and variant detection, this test has high potential as a point-of-care Ag-RDT in various settings when molecular assays are in limited supply and rapid diagnosis of SARS-CoV-2 is necessary.

Funder

U.S. Department of Health and Human Services

Administration for Strategic Preparedness and Response

Biomedical Advanced Research and Development Authority

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference23 articles.

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5. World Health Organisation (2020). Laboratory Testing Strategy Recommendations for COVID-19 Interim Guidance, World Health Organization. Available online: https://apps.who.int/iris/handle/10665/331509.

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