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10.1556/1886.2020.00017

http://scihub22266oqcxt.onion/10.1556/1886.2020.00017
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32804668!7592518!32804668
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suck abstract from ncbi


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pmid32804668      Eur+J+Microbiol+Immunol+(Bp) 2020 ; 10 (3): 156-164
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  • Evaluation of the automated cartridge-based ARIES SARS-CoV-2 Assay (RUO) against automated Cepheid Xpert Xpress SARS-CoV-2 PCR as gold standard #MMPMID32804668
  • Tanida K; Koste L; Koenig C; Wenzel W; Fritsch A; Frickmann H
  • Eur J Microbiol Immunol (Bp) 2020[Aug]; 10 (3): 156-164 PMID32804668show ga
  • INTRODUCTION: To evaluate the automated cartridge-based PCR approach ARIES SARS-CoV-2 Assay targeting the ORF-sequence and the N-gene of SARS-CoV-2. METHODS: In line with the suggestions by Rabenau and colleagues, the automated ARIES SARS-CoV-2 Assay was challenged with strongly positive samples, weakly positive samples and negative samples. Further, intra-assay and inter-assay precision as well as the limit-of-detection (lod) were defined with quantified target RNA and DNA. The Cepheid Xpert Xpress SARS-Cov-2 Assay was used as gold standard. RESULTS: Concordance between the ARIES assay and the Cepheid assay was 100% for strongly positive samples and for negative samples, respectively. For weakly positive samples as confirmed applying the Cepheid assay, a relevant minority of 4 out of 15 samples (26.7%) went undetected by the ARIES assay. Intra- and inter-assay precision were satisfactory, while the lod was in the 103 DNA copies/reaction-range, in the 103 virus copies/reaction-range, or in the 103-104 free RNA copies/reaction-range in our hands. CONCLUSIONS: The automated ARIES assay shows comparable test characteristics as the Cepheid assay focusing on strongly positive and negative samples but a slightly reduced sensitivity with weakly positive samples. Decisions on diagnostic use should include considerations on the lod.
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