Decreased Sensitivity of Rapid Antigen Test Is Associated with a Lower Viral Load of Omicron than Delta SARS-CoV-2 Variant.

Microbiol Spectr

INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, Service, Department of Virology, Sorbonne Université, Paris, France.

Published: October 2022

AI Article Synopsis

  • Large-scale screening for SARS-CoV-2 is crucial for controlling outbreaks, but new variants like Delta and Omicron may affect the reliability of rapid diagnostic tests (RDTs).
  • A study compared clinical and virological data from Delta and Omicron infections and found that the sensitivity of RDTs was significantly lower for Omicron (53.8%) compared to Delta (74.7%).
  • The research revealed that higher viral loads (VL) were present in Delta cases, which correlated with better test performance, suggesting that RDT sensitivity varies based on the variant, and repeated testing may be necessary if Omicron is suspected.

Article Abstract

Large-scale screening for SARS-CoV-2 infection is an important tool for epidemic prevention and control. The appearance of new variants associated with specific mutations can call into question the effectiveness of rapid diagnostic tests (RDTs) deployed massively at national and international levels. We compared the clinical and virological characteristics of individuals infected by Delta or Omicron variants to assess which factors were associated with a reduced performance of RDT. A commercially available RDT as well as the evaluation of the viral load (VL) and the detection of replicate intermediates (RIs) were carried out retrospectively on positive SARS-CoV-2 nasopharyngeal specimens from health care workers of the Pitié-Salpêtrière Hospital infected by the Delta or Omicron variant between July 2021 and January 2022. Of the 205 samples analyzed (104 from individuals infected with Delta and 101 with Omicron), 176 were analyzed by RDT and 200 by RT-PCR for VL and RIs. The sensitivity of the TDR for Omicron was significantly lower than that observed for Delta (53.8% 74.7%, respectively,  < 0.01). Moreover, the Delta VL was significantly higher than that measured for Omicron (median Ct 21.2 24.1, respectively,  < 0.01) and associated with the positivity of the RDT in multivariate analysis. We demonstrate a lower RDT sensitivity associated with a lower VL at the time of diagnosis on Omicron-infected individuals in comparison to those infected with the Delta variant. This RDT lower sensitivity should be taken into account in the large-scale screening strategy and in particular in case of strong suspicion of infection where testing should be repeated. Previous reports have shown a variability in the diagnostic performance of RDTs. In the era of SARS-CoV-2 variants and the use of RDT, mutation associated with these variants could affect the test performance. We evaluate the sensitivity of the RDT Panbio COVID-19 Ag (Abbott) with two variants of concern (VOC), the Delta and Omicron variants. In order to investigate whether clinical characteristics or virological characteristics can affect this sensitivity, we collected clinical information and performed a specific RT-PCR that detected the RIs as a marker of the viral replication and viral cycle stage. Our results showed that Omicron was less detected than the Delta variant. A lower viral load of Omicron variant in comparison to Delta variant explained this decreased sensitivity, even if they are at the same stage of the disease and the viral cycle and should be taken into account with the use of RDT as diagnostic tool.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9603576PMC
http://dx.doi.org/10.1128/spectrum.01922-22DOI Listing

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