Evaluation of RIDA®GENE Norovirus GI/GII Real Time RT-PCR Using Stool Specimens Collected from Children and Adults with Acute Gastroenteritis

Publication date: Available online 10 April 2018
Source:Journal of Clinical Virology
Author(s): N. Kanwar, F. Hassan, L. Barclay, C. Langley, J. Vinjé, P.W. Bryant, K. St. George, L. Mosher, J.M. Matthews-Greer, M.A. Rocha, D.O. Beenhouwer, C.J. Harrison, M. Moffatt, N. Shastri, R. Selvarangan
BackgroundNorovirus is the leading cause of epidemic and sporadic acute gastroenteritis (AGE) in the United States. Widespread prevalence necessitates implementation of accurate norovirus detection assays in clinical diagnostic laboratories.ObjectiveTo evaluate RIDA^®GENE norovirus GI/GII real-time RT-PCR assay (RGN RT-PCR) using stool samples from patients with sporadic AGE.Study designPatients between 14 days to 101 years of age with symptoms of AGE were enrolled prospectively at four sites across the United States during 2014-2015. Stool specimens were screened for the presence of norovirus RNA by the RGN RT-PCR assay. Results were compared with a reference method that included conventional RT-PCR and sequencing of a partial region of the 5'end of the norovirus ORF2 gene.ResultsA total of 259 (36.0%) of 719 specimens tested positive for norovirus by the reference method. The RGN RT-PCR assay detected norovirus in 244 (94%) of these 259 norovirus positive specimens. The sensitivity and specificity (95% confidence interval) of the RGN RT-PCR assay for detecting norovirus genogroup (G) I was 82.8% (63.5-93.5) and 99.1% (98.0-99.6) and for GII was 94.8% (90.8-97.2) and 98.6% (96.9-99.4), respectively. Seven specimens tested positive by the RGN-RT PCR that were negative by the reference method. The fifteen false negative samples were typed as GII.4 Sydney, GII.13, GI.3, GI.5, GI.2, GII.1, and GII.3 in the reference method.ConclusionsThe RGN RT-PCR assay had a high sensitivity and specificity for the detection of norovirus in stool specimens from patients with sporadic AGE.



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