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. 2020 Jul 24;15(7):e0236564. doi: 10.1371/journal.pone.0236564

Table 1. Direct RT-qPCR on SARS-CoV-2 positive and negative NPFS specimens after heating at 65°C for 10 minutes with different RT-qPCR master mixes.

Sample No. SARS-CoV-2 CT
Standard method Quantifast Pathogen RT-PCR + IC Master Mix PrimeDirect Probe RT-qPCR Mix TaqPath 1-Step RT-qPCR Master Mix
1 21.5 29.4 24.6 22.8
2 34.5 Undetermined Undetermined 35.3
3 24.5 30.4 28.7 25.5
4 22 29.9 31.4 25.8
5 Undetermined Undetermined Undetermined Undetermined

NPFS specimens were either subjected to viral RNA extraction by standard method using the NucliSENS easyMAG automated extraction system (bioMerieux), or diluted 4-fold with NFW followed by incubation at 65°C for 5 minutes. All samples were tested for SARS-CoV-2 RNA by standard RT-qPCR using different master mixes in duplicate and mean CT values were compared.