September through October 2010 multi-centre study in the Netherlands examining laboratory ability to detect enterovirus 68, an emerging respiratory pathogen

► Respiratory pathogen enterovirus 68 is phenotypic and genotypic alike rhinovirus. ► Rhinovirus RT-PCR assays of 8/11 laboratories were positive with enterovirus 68. ► Enterovirus two-step RT-PCR assays were more sensitive than one-step RT-PCR assays. ► Enterovirus 68 is likely underreported due to...

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Published in:Journal of virological methods Vol. 190; no. 1-2; pp. 53 - 62
Main Authors: Jaramillo-Gutierrez, Giovanna, Benschop, Kimberley S.M., Claas, Eric C.J., de Jong, Arjan S., van Loon, Anton M., Pas, Suzan D., Pontesilli, Oscar, Rossen, John W., Swanink, Caroline M.A., Thijsen, Steven, van der Zanden, Adri G.M., van der Avoort, Harrie G.A.M., Koopmans, Marion P.G., Meijer, Adam
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 01-06-2013
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Summary:► Respiratory pathogen enterovirus 68 is phenotypic and genotypic alike rhinovirus. ► Rhinovirus RT-PCR assays of 8/11 laboratories were positive with enterovirus 68. ► Enterovirus two-step RT-PCR assays were more sensitive than one-step RT-PCR assays. ► Enterovirus 68 is likely underreported due to positivity in rhinovirus RT-PCR. ► Molecular diagnosis of respiratory disease should include enterovirus detection. During September and October 2010, the Dutch Public Health Institute detected an enterovirus (EV) 68 (EV68) epidemic in the Netherlands through general practitioner-based surveillance of acute respiratory infections. EV68 shares phenotypic and genotypic properties with human rhinovirus (HRV). Despite increased EV and HRV detections, Dutch clinical laboratories did not identify EV68. To assess the capability of Dutch clinical laboratories to detect EV68, ten laboratories with more than eight detected EV and HRV cases in September and October 2010 provided information about their detection algorithms and testing results for a 2010 Dutch EV68 strain. For EV detection mostly stool specimens (median 49%), respiratory specimens (median 27%) and cerebrospinal fluid (median 22%) were used. For HRV detection only respiratory specimens were used. Except for the Seeplex® RV15ACE EV-specific assay, all EV and 73% of HRV assays, including those of the Public Health Institute, were able to detect EV68. Two-step EV RT-PCR protocols were the most sensitive. Thus, laboratories might have misidentified EV68 as HRV. In addition, EV68 cases might have also been missed because patients with respiratory diseases are usually not tested for EV infection. Therefore, clinical laboratories should include EV detection in the differential diagnosis of patients presenting with respiratory symptoms.
Bibliography:http://dx.doi.org/10.1016/j.jviromet.2013.02.010
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ISSN:0166-0934
1879-0984
DOI:10.1016/j.jviromet.2013.02.010