Author: Vogels, Chantal B F; Brito, Anderson F; Wyllie, Anne L; Fauver, Joseph R; Ott, Isabel M; Kalinich, Chaney C; Petrone, Mary E; Casanovas-Massana, Arnau; Catherine Muenker, M; Moore, Adam J; Klein, Jonathan; Lu, Peiwen; Lu-Culligan, Alice; Jiang, Xiaodong; Kim, Daniel J; Kudo, Eriko; Mao, Tianyang; Moriyama, Miyu; Oh, Ji Eun; Park, Annsea; Silva, Julio; Song, Eric; Takahashi, Takehiro; Taura, Manabu; Tokuyama, Maria; Venkataraman, Arvind; Weizman, Orr-El; Wong, Patrick; Yang, Yexin; Cheemarla, Nagarjuna R; White, Elizabeth B; Lapidus, Sarah; Earnest, Rebecca; Geng, Bertie; Vijayakumar, Pavithra; Odio, Camila; Fournier, John; Bermejo, Santos; Farhadian, Shelli; Dela Cruz, Charles S; Iwasaki, Akiko; Ko, Albert I; Landry, Marie L; Foxman, Ellen F; Grubaugh, Nathan D
                    Title: Analytical sensitivity and efficiency comparisons of SARS-CoV-2 RT-qPCR primer-probe sets.  Cord-id: s1hvcpaq  Document date: 2020_7_10
                    ID: s1hvcpaq
                    
                    Snippet: The recent spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) exemplifies the critical need for accurate and rapid diagnostic assays to prompt clinical and public health interventions. Currently, several quantitative reverse transcription-PCR (RT-qPCR) assays are being used by clinical, research and public health laboratories. However, it is currently unclear whether results from different tests are comparable. Our goal was to make independent evaluations of primer-probe sets
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: The recent spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) exemplifies the critical need for accurate and rapid diagnostic assays to prompt clinical and public health interventions. Currently, several quantitative reverse transcription-PCR (RT-qPCR) assays are being used by clinical, research and public health laboratories. However, it is currently unclear whether results from different tests are comparable. Our goal was to make independent evaluations of primer-probe sets used in four common SARS-CoV-2 diagnostic assays. From our comparisons of RT-qPCR analytical efficiency and sensitivity, we show that all primer-probe sets can be used to detect SARS-CoV-2 at 500 viral RNA copies per reaction. The exception for this is the RdRp-SARSr (Charité) confirmatory primer-probe set which has low sensitivity, probably due to a mismatch to circulating SARS-CoV-2 in the reverse primer. We did not find evidence for background amplification with pre-COVID-19 samples or recent SARS-CoV-2 evolution decreasing sensitivity. Our recommendation for SARS-CoV-2 diagnostic testing is to select an assay with high sensitivity and that is regionally used, to ease comparability between outcomes.
 
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