Detection of Listeria monocytogenes in vacuum-packed meat products using real-time PCR, immunoassay and culturing

被引:3
作者
Netschajew, Andrej [2 ]
Fredriksson-Ahomaa, Maria [1 ]
Sperner, Brigitte [1 ]
Stolle, Andreas [1 ]
机构
[1] Univ Munich, Lehrstuhl Hyg & Technol Lebensmittel Tier Ursprun, Tierarztl Fak, D-85764 Oberschleissheim, Germany
[2] Staatl Akad Vet Med, St Petersburg, Russia
来源
ARCHIV FUR LEBENSMITTELHYGIENE | 2009年 / 60卷 / 01期
关键词
Listeria monocytogenes; meat products; real-time PCR; VIDAS; FOOD; EPIDEMIOLOGY; ENUMERATION; SAUSAGES; SAMPLES; FRESH;
D O I
10.2376/0003-925X-60-12
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
During the past ten years, several Listeria (L.) monocytogenes outbreaks with febrile gastroenteritis as the predominant clinical manifestation affecting healthy adults have been reported. The main transmission route to humans is believed to be through consumption of contaminated food, especially ready-to-eat (RTE) foods. Rapid and specific detection of L. monocytogenes in food is critical for ensuring the safety of consumers. The aim of this work was to study the occurrence of L. monocytogenes in vacuum-packed meat products using real-time PCR, immunoassay and culturing. In total, 50 vacuum-packed meat products collected 2007 were studied using real-time PCR (iQ-Check (TM) real-time PCR kit), immunoassay (VIDAS LMO2 test) and culturing (L 00.00-22:1998, Official Collection of Examination Methods according to 64 LFGB). Thirty-two of 50 (64%) vacuum-packed meat products were L. monocytogenes positive by real-time PCR. The occurrence was especially high in heat-treated sausages (80%). Only two products (two bacons) were VIDAS and culture positive. Additionally, L. monocytogenes was isolated from one heat-treated sausage, which was VIDAS negative. All VIDAS and culture-positive samples were also PCR positive. In two (12%) out of 17 vacuum-packed RTE products, the number of L. monocytogenes was over 100 cfu/g demonstrating that the shelf life assigned to some vacuum-packed products is not appropriate. Real-time PCR based on iQ-Check (TM) real-time PCR kit was shown to be very sensitive to detect L. monocytogenes in foods and thus a useful tool for screening.
引用
收藏
页码:12 / 17
页数:6
相关论文
共 28 条
[11]   History and epidemiology of listeriosis [J].
Hof, H .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2003, 35 (03) :199-202
[12]  
*ISO, 2004, HOR METH DET EN LI 1
[13]   Listeria monocytogenes in multiple habitats and host populations:: Review of available data for mathematical modeling [J].
Ivanek, Renata ;
Groehn, Yrjoe T. ;
Wiedmann, Martin .
FOODBORNE PATHOGENS AND DISEASE, 2006, 3 (04) :319-336
[14]   Preparation of Listeria monocytogenes specimens for molecular detection and identification [J].
Liu, Dongyou .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2008, 122 (03) :229-242
[15]   Validation of NMKL method No. 136 -: Listeria monocytogenes, detection and enumeration in foods and feed [J].
Loncarevic, S. ;
Okland, M. ;
Sehic, E. ;
Norli, H. S. ;
Johansson, T. .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2008, 124 (02) :154-163
[16]   Incidence and control of Listeria monocytogenes in foods in Denmark [J].
Norrung, B ;
Andersen, JK ;
Schlundt, J .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1999, 53 (2-3) :195-203
[17]   Rapid real-time PCR detection of Listeria monocytogenes in enriched food samples based on the ssr A gene, a novel diagnostic target [J].
O' Grady, Justin ;
Sedano-Balbas, Sara ;
Maher, Majella ;
Smith, Terry ;
Barry, Thomas .
FOOD MICROBIOLOGY, 2008, 25 (01) :75-84
[18]   Limitation in the detection of Listeria monocytogenes in food in the presence of competing Listeria innocua [J].
Oravcova, K. ;
Trncikova, T. ;
Kuchta, T. ;
Kaclikova, E. .
JOURNAL OF APPLIED MICROBIOLOGY, 2008, 104 (02) :429-437
[19]   A novel real-time PCR-based method for the detection of Listeria monocytogenes in food [J].
Oravcova, K. ;
Kuchta, T. ;
Kaclikova, E. .
LETTERS IN APPLIED MICROBIOLOGY, 2007, 45 (05) :568-573
[20]   Detection, quantification and vitality of Listeria monocytogenes in food as detennined by quantitative PCR [J].
Rantsiou, Kalliopi ;
Alessandria, Valentina ;
Urso, Rosalinda ;
Dolci, Paola ;
Cocolin, Luca .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2008, 121 (01) :99-105