Journal Home
Search for

Volume 60, Issue 5, Pages 354-359 (May 2010)


View previous. 7 of 18 View next.

A new multiplex PCR assay for the simultaneous detection of vancomycin-resistant enterococci from rectal swabs

Dona Benadofa, Marcela San Martínb, Judith Aguirrea, Liliana Paredesb, Rodrigo Maligc, Francisco Melod, Gaëlle LehouquecCorresponding Author Informationemail address

Accepted 24 February 2010. published online 29 March 2010.

Summary 

Objectives

This study describes the diagnostic performance of a recently available multiplex PCR-based kit for the simultaneous detection and identification of Enterococcus faecium, Enterococcus faecalis, vanA, vanB, vanC1 and vanC2/C3 genes, directly from rectal swabs constituting the most complete existing molecular assay currently available.

Methods

The diagnostic performance of this assay was evaluated by a multicenter study involving three independent public hospitals and consisted in the analysis of 187 rectal swabs from patients at high risk for vancomycin-resistant enterococci colonization.

Results

When bacteria culture was used as the gold standard, the sensitivity, specificity, positive and negative predicted values for the assay were 96.8%, 76.0%, 67.7% and 97.9%, respectively. When a composite reference standard consisting of culture and DNA sequencing of PCR products was used as the gold standard, the sensitivity, specificity, positive and negative predicted values for the PCR-based assay were 97.8%, 96.9%, 96.7% and 97.9%, respectively.

Conclusions

Based on these results, we conclude that this assay is considerably more sensitive than traditional microbiological methods for detecting vancomycin-resistant enterococci from rectal swabs. It is also much faster than culture. We believe that the implementation of this assay in routine clinical laboratories could help to reduce hospital-acquired vancomycin-resistant enterococci infections.

a Laboratorio de Microbiología, Roberto del Rio Hospital, Zañartu Ave. 1085, Santiago, Chile

b Laboratorio de Microbiología, Barros Luco Trudeau Hospital, José Miguel Carrera Ave. 3204, Santiago, Chile

c Departamento de Investigación y Desarrollo, TAAG Genetics S.A., Antonio Bellet 77, Of. 703. Providencia, Santiago, Chile

d Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Alameda 340, Santiago, Chile

Corresponding Author InformationCorresponding author. Tel.: +56 2 264 38 76, fax: +56 2 264 27 95.

PII: S0163-4453(10)00054-X

doi:10.1016/j.jinf.2010.02.011


View previous. 7 of 18 View next.