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    Test results of serotyping Salmonella strains in the Member States of the European Union (A collaborative study amongst the National Reference Laboratories for Salmonella)

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    Authors
    Voogt N
    Maas HME
    Leeuwen WJ van
    Henken AM
    Series/Report no.
    RIVM rapport 284500008
    Type
    Report
    Language
    en
    
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    Title
    Test results of serotyping Salmonella strains in the Member States of the European Union (A collaborative study amongst the National Reference Laboratories for Salmonella)
    Translated Title
    Serotyperingsuitslagen van Salmonella stammen in de lidstaten van de Europese Unie (Een ringonderzoek met de Nationale Referentie Laboratoria voor Salmonella)
    Publiekssamenvatting
    A second collaborative study on Salmonella serotyping was organised by the Community Reference Laboratory (CRL) for Salmonella, with participation of the National Reference Laboratories (NRLs) for Salmonella from 14 of the 15 Member States of the European Union. The objective of the study was to investigate the capacity of the NRLs for correctly identifying serovars of Salmonella enterica subsp. enterica. Twenty serovars of Salmonella enterica subsp. enterica selected by the CRL had to be examined by all NRLs according to their routine serotyping method. Thanks to the use of many frequently occurring serovars and the possibility of NRLs to send strains to another specialized laboratory, better results were obtained than for an earlier study. The incorrect detection of H antigens was the reason for most of the incorrect identifications.
    Het Communautair Referentie Laboratorium (CRL) voor Salmonella heeft een ringonderzoek voor de serotypering van Salmonella georganiseerd. De Nationale Referentie Laboratoria (NRLs) voor Salmonella uit 14 van de 15 lidstaten van de Europese Unie deden aan het onderzoek mee. Het doel was te onderzoeken of de NRLs serotypen van Salmonella enterica subsp. enterica correct konden identificeren. Twintig serotypen van Salmonella enterica subsp. enterica werden door het CRL geselecteerd. Deze moesten door de NRLs met de routinematig gebruikte serotyperingsmethode worden onderzocht. Door het gebruik van veel voorkomende serotypen en de mogelijkheid voor een NRL stammen door te sturen naar een ander gespecialiseerd laboratorium, werden betere resultaten verkregen vergeleken met een eerder ringonderzoek. De reden voor de meeste incorrecte identificaties was een incorrecte detectie van H antigenen.
    Publisher
    Rijksinstituut voor Volksgezondheid en Milieu RIVM
    URI
    http://hdl.handle.net/10029/9961
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    RIVM official reports

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