Viruses (Oct 2021)

The Value of Rapid Antigen Tests for Identifying Carriers of Viable SARS-CoV-2

  • Elena V. Shidlovskaya,
  • Nadezhda A. Kuznetsova,
  • Elizaveta V. Divisenko,
  • Maria A. Nikiforova,
  • Andrei E. Siniavin,
  • Daria A. Ogarkova,
  • Aleksandr V. Shagaev,
  • Maria A. Semashko,
  • Artem P. Tkachuk,
  • Olga A. Burgasova,
  • Vladimir A. Gushchin

DOI
https://doi.org/10.3390/v13102012
Journal volume & issue
Vol. 13, no. 10
p. 2012

Abstract

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The search for effective methods to detect patients who excrete a viable virus is one of the urgent tasks of modern biomedicine. In the present study, we examined the diagnostic value of two antigen tests, BIOCREDIT COVID-19 Ag (RapiGEN Inc., Anyang, Korea) and SGTI-flex COVID-19 Ag (Sugentech Inc., Cheongju, Korea), for their diagnostic value in identifying patients who excrete viable SARS-CoV-2. As part of the study, we examined samples from 106 patients who had just been admitted to the hospital and who had undergone quantitative RT-PCR and assessment of viability of SARS-CoV-2 using cell culture. Assessment of the tests’ value for detecting samples containing viable virus showed high sensitivity for both tests. Sensitivity was 78.6% (95% CI, from 49.2% to 95.3%) for SGTI-flex COVID-19 Ag and 100% (95% CI, from 76.8% to 100%) for Biocredit COVID-19 Ag. The specificity of rapid tests was significantly higher than that of RT-PCR and was 66.3% (95% CI, from 55.7% to 75.8%) and 67.4% (95% CI, from 56.8% to 76.8%) for SGTI-flex COVID-19 Ag and Biocredit COVID-19 Ag versus 30.4% (95% CI, from 21.3% to 40.9%) obtained for PCR. Thus, for tasks of identifying viable SARS-CoV-2 during screening of conditionally healthy people, as well as monitoring those quarantined, rapid tests show significantly better results.

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