International Collaborative Study To Compare Reverse Transcriptase PCR Assays for Detection and Genotyping of Noroviruses

Author:

Vinjé Jan1,Vennema Harry1,Maunula Leena2,von Bonsdorff Carl-Henrik2,Hoehne Marina3,Schreier Eckart3,Richards Alison4,Green Jon4,Brown David4,Beard Suzanne S.5,Monroe Stephan S.5,de Bruin Erwin1,Svensson Lennart6,Koopmans Marion P. G.1

Affiliation:

1. Research Laboratory for Infectious Diseases, National Institute of Public Health and the Environment, Bilthoven, The Netherlands

2. Haartman Institute, Department of Virology, Helsinki, Finland

3. Robert Koch-Institute, Berlin, Germany

4. Central Public Health Laboratory, London, United Kingdom

5. Viral Gastroenteritis Section, Centers for Disease Control and Prevention, Atlanta, Georgia

6. Swedish Institute for Infectious Disease Control, Solna, Sweden

Abstract

ABSTRACT To allow more rapid and internationally standardized assessment of the spread of noroviruses (previously called Norwalk-like viruses [NLVs]) as important food-borne pathogens, harmonization of methods for their detection is needed. Diagnosis of NLVs in clinical diagnostic laboratories is usually performed by reverse transciptase PCR (RT-PCR) assays. In the present study, the performance of five different RT-PCR assays for the detection of NLVs was evaluated in an international collaborative study by five laboratories in five countries with a coded panel of 91 fecal specimens. The assays were tested for their sensitivity, detection limit, and ease of standardization. In total, NLVs could be detected by at least one RT-PCR assay in 69 (84%) of the samples that originally tested positive. Sensitivity ranged from 52 to 73% overall and from 54 to 100% and 58 to 85% for genogroup I and II viruses, respectively. In all, 64% of the false-negative results were obtained with a set of diluted stools ( n = 20) that may have lost quality upon storage. Sensitivity was improved when these samples were excluded from analysis. No one single assay stood out as the best, although the p1 assay demonstrated the most satisfactory overall performance. To promote comparability of data, this assay will be recommended for newly starting groups in future collaborative studies.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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