Author: Goncharova, Ekaterina A.; Dedkov, Vladimir G.; Dolgova, Anna S.; Kassirov, Ilia S.; Safonova, Marina V.; Voytsekhovskaya, Yana; Totolian, Areg A.
Title: Oneâ€step quantitative RTâ€PCR assay with armored RNA controls for detection of SARSâ€CoVâ€2 Cord-id: dzpn1159 Document date: 2020_10_5
ID: dzpn1159
Snippet: Coronavirus disease 2019 (COVIDâ€19) has become pandemic since March 11, 2020. Thus, development and integration in clinics of fast and sensitive diagnostic tools are essential. The aim of the study is a development and evaluation of a oneâ€step quantitative reverse transcriptionâ€polymerase chain reaction (RTâ€qPCR) assay (COVIDâ€19 Amp) for severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) detection with an armored positive control and internal controls constructed from syn
Document: Coronavirus disease 2019 (COVIDâ€19) has become pandemic since March 11, 2020. Thus, development and integration in clinics of fast and sensitive diagnostic tools are essential. The aim of the study is a development and evaluation of a oneâ€step quantitative reverse transcriptionâ€polymerase chain reaction (RTâ€qPCR) assay (COVIDâ€19 Amp) for severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) detection with an armored positive control and internal controls constructed from synthetic MS2â€phageâ€based RNA particles. The COVIDâ€19 Amp assay limit of detection was 10(3) copies/ml, the analytical specificity was 100%. A total of 109 biological samples were examined using COVIDâ€19 Amp and World Health Organization (WHO)â€based assay. Discordance in nine samples was observed (negative by the WHOâ€based assay) and discordant samples were retested as positive according to the results obtained from the Vectorâ€PCRrvâ€2019â€nCoVâ€RG assay. The developed COVIDâ€19 Amp assay has high sensitivity and specificity, includes virus particlesâ€based controls, provides the direct definition of the SARSâ€CoVâ€2 RdRp gene partial sequence, and is suitable for any hospital and laboratory equipped for RTâ€qPCR.
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