Evaluation of the clinical and analytical performance of the Seegene allplexTM SARS-CoV-2 variants I assay for the detection of variants of concern (VOC) and variants of interests (VOI)

Background: High-throughput assays for the detection of SARS-CoV-2 variants of concern (VOC) and interest (VOI) are a diagnostic alternative when whole genome sequencing (WGS) is unavailable or limited. Objective: This study evaluated the clinical and analytical performance of the Seegene AllplexTM SARS-CoV-2 Variants I assay, which detects the HV69/70 deletion, N501Y and E484K mutations of the S gene. Methods: Genotyping was evaluated on-871 SARS-CoV-2 RNA positive specimens, 408 nasopharyngeal (NP) swabs and 463 saline gargle (SG) specimens, with WGS used as the reference standard. Analytical performance was assessed including stability, reproducibility, limit of detection (LOD), cross-reactivity and interference with various respiratory microorganisms. Results: The clinical study revealed sensitivity of 100% (95% CI 99.27%-100%) and specificity of 100% (95% CI 98.99%-100%) for HV69/70 deletion, sensitivity of 100% (95% CI 99.55%-100%) and specificity of 100% (95% CI 93.73% - 100%) for N501Y, and sensitivity of 100% (95% CI 98.94% - 100%) and specificity of 98.10% (95% CI 96.53% - 99.08%) for E484K mutation. The E484Q mutation was detected in 10 specimens of the Kappa variant (B.1.627.1). Analytical performance demonstrated stability and reproducibility over 7 days, and LOD was calculated at 698 cp/mL for NP swab specimens, and 968 cp/mL for SG specimens. No interference or cross reactivity with other microorganisms was noted. Conclusion: The AllplexTM SARS-CoV-2 Variants I assay is acceptable for clinical use for the detection of variant of concern and variant of interest.

Automated summary

The Seegene AllplexTM SARS-CoV-2 Variants I assay shows 100% sensitivity and specificity for detecting the HV69/70 deletion, N501Y, and E484K mutations of the S gene of SARS-CoV-2. The assay is found to be stable, reproducible, and has a high limit of detection, making it acceptable for clinical use in detecting variants of concern and interest.