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. 2022 May 26;17(5):e0268692. doi: 10.1371/journal.pone.0268692

Table 1. Direct comparison of SARS-CoV-2 detection using RT-qPCR and extraction-free RT-LAMP.

Samples Purified Saliva RNA Saliva Lysate
RT-qPCR N1 (Cq) RT-qPCR N2 (Cq) COVID LAMP (Tt) COVID LAMP (Tt)
1 24.8 24.8 24.2 24.3 8.9 8.9 8.7 8.6
2 26.2 26.3 25.8 25.8 9.9 9.9 9.8 10.1
3 27.3 27.2 26.9 27.0 8.5 8.4 10.7 10.3
4 28.6 28.7 28.2 28.2 9.5 9.6 9.4 9.4
5 30.1 30.2 29.8 29.8 9.2 8.9 10.7 10.3
6 31.6 31.7 31.1 31.1 9.4 9.2 13.3 11.5
7 31.7 32.0 31.2 31.6 10.3 9.8 11.3 11.0
8 32.0 32.0 31.3 31.3 9.5 9.6 12.0 11.9
9 32.9 33.3 36.1 36.5 12.1 12.0 13.6 13.6
10 34.3 34.5 33.4 34.0 10.3 10.9 10.6 11.6
11 34.7 34.7 N/A N/A 14.0 13.3 16.5 14.7
12 35.3 35.5 35.4 35.2 12.0 11.7 22.9 N/A
13 37.5 N/A N/A N/A N/A N/A 16.4 N/A
14 37.8 37.5 37.9 38.3 13.8 28.4 N/A N/A
15 38.4 38.1 N/A N/A N/A 19.8 N/A N/A
16 38.8 39.1 N/A N/A N/A N/A N/A N/A

16 saliva samples containing a range of viral load were tested in RT-qPCR (N1 and N2 targets) and RT-LAMP(SARS-CoV-2). For RT-LAMP, both saliva lysate and purified RNA were used as input, whereas RT-qPCR was performed using only purified RNA. Cq values for RT-qPCR and Tt for RT-LAMP are shown. No amplification is denoted N/A.