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Validation of EN ISO method 10273 - Detection of pathogenic Yersinia enterocolitica in foods.
Hallanvuo, Saija; Herranen, Mirkka; Jaakkonen, Anniina; Nummela, Maria; Ranta, Jukka; Botteldoorn, Nadine; De Zutter, Lieven; Fredriksson-Ahomaa, Maria; Hertwig, Stefan; Johannessen, Gro S; Ludewig, Martina; Messelhäußer, Ute; Sigvart-Mattila, Pia; Thisted-Lambertz, Susanne; Thure, Tiina; Vatunen, Elina.
Afiliação
  • Hallanvuo S; Food and Feed Microbiology Research Unit, Research and Laboratory Services Department, Finnish Food Safety Authority Evira, Mustialankatu 3, 00790, Helsinki, Finland. Electronic address: saija.hallanvuo@evira.fi.
  • Herranen M; Food and Feed Microbiology Research Unit, Research and Laboratory Services Department, Finnish Food Safety Authority Evira, Mustialankatu 3, 00790, Helsinki, Finland.
  • Jaakkonen A; Food and Feed Microbiology Research Unit, Research and Laboratory Services Department, Finnish Food Safety Authority Evira, Mustialankatu 3, 00790, Helsinki, Finland.
  • Nummela M; Food and Feed Microbiology Research Unit, Research and Laboratory Services Department, Finnish Food Safety Authority Evira, Mustialankatu 3, 00790, Helsinki, Finland.
  • Ranta J; Risk Assessment Research Unit, Research and Laboratory Services Department, Finnish Food Safety Authority Evira, Mustialankatu 3, 00790 Helsinki, Finland.
  • Botteldoorn N; Service food pathogens, Institute of Public health, Juliette Wijtsmans street 14, 1050 Brussels, Belgium.
  • De Zutter L; Department of Veterinary Public Health and Food Safety, Faculty of Veterinary Medicine, Ghent University, Salisburylaan, 133, 9820 Merelbeke, Belgium.
  • Fredriksson-Ahomaa M; Faculty of Veterinary Medicine, University of Helsinki, P.O. Box 66, FI-00014, Finland.
  • Hertwig S; Federal Institute for Risk Assessment (BfR), Diedersdorfer Weg 1, 12277 Berlin, Germany.
  • Johannessen GS; Norwegian Veterinary Institute, Ullevålsveien 68, 0454 Oslo, Norway.
  • Ludewig M; Institute of Food Hygiene, Faculty of Veterinary Medicine, University of Leipzig, An den Tierkliniken 1, 04103 Leipzig, Germany.
  • Messelhäußer U; Laboratory of food microbiology, Bavarian Health and Food Safety Authority, Veterinärstr. 2, 85764 Oberschleißheim, Germany.
  • Sigvart-Mattila P; Water Protection Association of the River Kokemäki, Patamäenkatu 24, 33900 Tampere, Finland.
  • Thisted-Lambertz S; Microbiology division, National Food Agency, Strandbodgatan 4, 75323 Uppsala, Sweden.
  • Thure T; Metropolilab Oy, Viikinkaari 4, 00790 Helsinki, Finland.
  • Vatunen E; Finnish Customs Laboratory, Tekniikantie 13, 02150 Espoo, Finland.
Int J Food Microbiol ; 288: 66-74, 2019 Jan 02.
Article em En | MEDLINE | ID: mdl-29395387
ABSTRACT
EN ISO 10273 method for the detection of pathogenic Yersinia enterocolitica in foods was validated in the project Mandate M/381 funded by European Commission. A total of 14 laboratories from five European countries participated in the interlaboratory study (ILS) organized during 2013 and 2014. Before the ILS, the method was revised by an international group of experts and the performance of the revised method was assessed in an ILS study. The results are published as a part of the standard EN ISO 10273 revision. The study included three rounds with different sample types; raw milk, iceberg lettuce and minced meat, inoculated with a low and high level of pathogenic Y. enterocolitica strains representing major pathogenic bioserotypes 4/O3 and 2/O9. The homogeneity and stability of the samples were verified before dispatching them to the laboratories. The results demonstrated the method sensitivity of 96% in raw milk, 97% in minced meat, and 98% in lettuce at high inoculation level of pathogenic Y. enterocolitica. The specificity was 100% in raw milk, 96% in minced meat, and 98% in lettuce. The level of detection, LOD50, varied between study rounds, being 9.4 CFU/25 ml in raw milk, 9.9 CFU/25 g in minced meat and 63 CFU/25 g in lettuce samples. During the study, confirmation by using real-time PCR method ISO/TS 18867 together with pyrazinamidase testing was also validated, as alternative to conventional biochemical confirmation. When comparing different isolation steps used in the revised method during the study rounds, PSB enrichment and plating on CIN after alkaline (KOH) treatment showed the highest sensitivity (52-92%) in raw milk and minced meat samples. In lettuce samples, however, ITC with KOH treatment before plating on CIN showed higher sensitivity (64% at low level; 82% at high level) than plating on CIN from PSB with KOH treatment (44% at low level; 74% at high level). Statistical analysis of different isolation steps supported the use of two enrichment media, PSB and ITC, in the revised method. Recovery of pathogenic Y. enterocolitica on CIN was most efficient after KOH treatment and, based on the analysis, plating on CIN agar without KOH treatment could be left as optional procedure in the method.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Yersinia enterocolitica / Microbiologia de Alimentos Tipo de estudo: Diagnostic_studies Limite: Animals País/Região como assunto: Europa Idioma: En Revista: Int J Food Microbiol Assunto da revista: CIENCIAS DA NUTRICAO / MICROBIOLOGIA Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Yersinia enterocolitica / Microbiologia de Alimentos Tipo de estudo: Diagnostic_studies Limite: Animals País/Região como assunto: Europa Idioma: En Revista: Int J Food Microbiol Assunto da revista: CIENCIAS DA NUTRICAO / MICROBIOLOGIA Ano de publicação: 2019 Tipo de documento: Article