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European validation of Real-Time PCR method for detection of Salmonella spp. in pork meat

Authors :
Javier Butrón
Patricia González-García
Džiuginta Jakočiūnė
Antonietta Gattuso
Dario De Medici
Françoise Le Gall
John Elmerdahl Olsen
Frederique Pasquali
Ségolène Quesne
Claudia Zampieron
Gro S. Johannessen
Enrico Pavoni
Alessandra De Cesare
Danijela Horvatek Tomić
Marianne Chemaly
Elisabetta Delibato
Estella Prukner-Radovčić
Zuzsanna Sreter-Lancz
Barbara Bertasi
Gerardo Manfreda
David Rodríguez-Lázaro
Federico Capuano
Paola De Santis
M. Gianfranceschi
Maja Lukač
Javier Pérez-De-Juan
Marta Hernández
Sarah Lovari
Antonia Anna Lettini
María-José Saiz-Abajo
Michele Sonnessa
Damiano Comin
Yolande Therese Rose Proroga
Elisabetta Delibato
David Rodriguez Lazaro
Monica Gianfranceschi
Alessandra De Cesare
Damiano Comin
Antonietta Gattuso
Marta Hernandez
Michele Sonnessa
Frédérique Pasquali
Zuzsanna Sreter-Lancz
María-José Saiz-Abajo
Javier Pérez-De-Juan
Javier Butrón
Estella Prukner-Radovcic
Danijela Horvatek Tomic
Gro S. Johannessen
Džiuginta Jakočiūnė
John E. Olsen
Marianne Chemaly
Francoise Le Gall
Patricia González-García
Antonia Anna Lettini
Maja Lukac
Segolénè Quesne
Claudia Zampieron
Paola De Santi
Sarah Lovari
Barbara Bertasi
Enrico Pavoni
Yolande T.R. Proroga
Federico Capuano
Gerardo Manfreda
Dario De Medici
Source :
International Journal of Food Microbiology
Publication Year :
2013

Abstract

The classical microbiological method for detection of Salmonella spp. requires more than five days for final confirmation, and consequently there is a need for an alternative methodology for detection of this pathogen particularly in those food categories with a short shelf-life. This study presents an international (at European level) ISO 16140-based validation study of a non-proprietary Real-Time PCR-based method that can generate final results the day following sample analysis. It is based on an ISO compatible enrichment coupled to an easy and inexpensive DNA extraction and a consolidated Real-Time PCR assay. Thirteen laboratories from seven European Countries participated to this trial, and pork meat was selected as food model. The limit of detection observed was down to 10 CFU per 25 g of sample, showing excellent concordance and accordance values between samples and laboratories (100%). In addition, excellent values were obtained for relative accuracy, specificity and sensitivity (100%) when the results obtained for the Real-Time PCR-based methods were compared to those of the ISO 6579:2002 standard method. The results of this international trial demonstrate that the evaluated Real-Time PCR-based method represents an excellent alternative to the ISO standard. In fact, it shows an equal and solid performance as well as it reduces dramatically the extent of the analytical process, and can be easily implemented routinely by the Competent Authorities and Food Industry laboratories.

Details

ISSN :
18793460
Volume :
184
Database :
OpenAIRE
Journal :
International journal of food microbiology
Accession number :
edsair.doi.dedup.....7930d283200a167c756476ae01c9f37b