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. 2008 Dec 1;75(3):618–624. doi: 10.1128/AEM.01507-08

TABLE 2.

Reproducibility of method B for NoV detection for six naturally contaminated samples, each extracted three times

Sample Genogroup I NoV
Genogroup II NoV
rRT-PCR efficiency (%)a Concnb (RNA copies/g DT)
rRT-PCR efficiency (%)a Concnb (RNA copies/g DT)
Assay 1 Assay 2 Assay 3 Assay 1 Assay 2 Assay 3
1 97.0 ± 1.7 330 +DLc 100.7 ± 0.6 16 43 38
2 95.6 ± 2.5 100.9 ± 2.6 +DL
3 94.8 ± 4.3 98.2 ± 5.2
4 96.7 ± 1.9 250 102.4 ± 0.3 110 +DL 88
5 97.6 ± 1.7 840 99.7 ± 3.9 190 58
6 94.8 ± 5.0 910 100.1 ± 1.8 110 +DL 53
a

rRT-PCR efficiency was calculated based on coamplification of genogroup I and II RNA external controls with pure and 10-fold-diluted nucleic acid extract.

b

The genogroup I or II NoV concentration was calculated based on CT values obtained for pure and 10-fold-diluted nucleic acid extract and the corresponding standard curve.

c

+DL, positive sample, but the level was too close to the limit of detection for quantification.