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Volume 47, Issue 1, Pages 54-59 (January 2010)


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Multicenter evaluation of the ENTEROVIRUS R-gene™ real-time RT-PCR assay for the detection of enteroviruses in clinical specimens

Sylvie Pilleta, Geneviève Billaudb, Shabir Omara, Bruno Linab, Bruno Pozzettoa, Isabelle SchuffeneckerbCorresponding Author Informationemail address

Received 22 September 2009; accepted 25 September 2009. published online 30 October 2009.

Abstract 

Background

The rapid molecular diagnosis of enteroviral meningitis has been shown important for an adequate management of the patients.

Objectives

A new CE-marked real-time RT-PCR assay (ENTEROVIRUS R-gene™, Argene) was evaluated in two university hospital virology laboratories.

Study design

Reactivity, analytical sensitivity and specificity were evaluated using 54 prototype and 173 clinical human enterovirus (HEV) strains, a 12-sample HEV proficiency panel, and 30 non-HEV microorganisms. The clinical performance of the ENTEROVIRUS R-gene™ assay was evaluated by testing 197 cerebrospinal fluid (CSF) and 103 respiratory specimens, comparatively to the routinely used diagnostic techniques.

Results

Sixty-four out of the 65 HEV serotypes tested were detected. The analytical sensitivity ranged between 10−2.64 and 102.39TCID50/50μl. Cross-reactivity was observed with four human rhinoviruses. On 59 CSF specimens analyzed prospectively, the results of the ENTEROVIRUS R-gene™ assay showed a 94.8% concordance with those of the Smart enterovirus (EV) assay (Cepheid). On 138 CSF specimens tested retrospectively, the results of the ENTEROVIRUS R-gene™ assay showed a 97.1% concordance with those of either the GeneXpert EV assay (Cepheid) or the in-house RT-PCR HEV assays used at the time of specimen collection. On 103 respiratory specimens, the concordance between the results of the ENTEROVIRUS R-gene™ assay and those of the routine RT-PCRs or viral culture was 90.2% and 96.1% before and after retest, respectively.

Conclusions

The new test was found able to detect a large panel of enterovirus serotypes; it was sensitive when used on clinical specimens; and, easy and rapid to perform on a routine basis.

a Laboratoire de Bactériologie-Virologie, GIMAP EA 3064 and University Hospital of Saint-Etienne, 42023 Saint-Etienne Cedex 2, France

b Centre National de Référence des Enterovirus, Laboratoire de Virologie Est des Hospices Civils de Lyon, Centre Hospitalier Universitaire de Lyon, 59 Boulevard Pinel, 69677 Bron Cedex, France

Corresponding Author InformationCorresponding author. Tel.: +33 4 72 12 96 47; fax: +33 4 72 12 95 00.

PII: S1386-6532(09)00481-8

doi:10.1016/j.jcv.2009.09.033


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