A multiparametric PCR-based tool for fast detection and identification of spore-forming bacteria in food

被引:14
|
作者
Postollec, Florence [1 ]
Bonilla, Stephane [2 ]
Baron, Florence [3 ]
Jan, Sophie [3 ]
Gautier, Michel [3 ]
Mathot, Anne Gabrielle [4 ]
Hallier-Soulier, Sylvie [2 ]
Pavan, Sonia
Sohier, Daniele
机构
[1] PHYSIOpt, ADRIA Dev, UMT 083, ZA Creach Gwen, F-29196 Quimper, France
[2] Pall GeneSyst, Bruz, France
[3] INRA, UMR 1253, Rennes, France
[4] France Univ Brest, Univ Europeenne Bretagne, Lab Univ Biodiversite & Ecol Microbienne, E43882,IFR148 ScinBios,UMT 083,PHYSiOpt, F-29334 Quimper, France
关键词
Spore-forming; Bacillus; Clostridium; PCR; Specificity; Validation; Food; Spoilage; BACILLUS-CEREUS GROUP; REAL-TIME PCR; CLOSTRIDIUM-TYROBUTYRICUM SPORES; SP-NOV; 100; MILLILITERS; RAW-MILK; GEN-NOV; PROPOSAL; STRAINS; RDNA;
D O I
10.1016/j.ijfoodmicro.2010.06.005
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The presence of psychrotrophic or highly thermoresistant spore-forming bacteria in food and feedstuff responsible for food poisoning and spoilage raises major safety and economical issues. The aim of this study was to evaluate the performances of a ready-to-use PCR assay (alternative method) in comparison with the standard microbiological plating method regarding spore-forming bacteria detection in food samples. An overnight sample enrichment was selected to increase sporeformer diversity recovery, spore germination, bacterial growth and favour DNA extraction. A total of 180 sporeformer isolates representing 38 different species and 8 genera were tested in the PCR assays. Inclusivity and exclusivity results ensured specific detection and identification of the majority of targeted genera and species. Validation studies carried on artificially contaminated food samples showed detection of the inoculated contaminants in most cases, with increased detection limit for the alternative method which enabled detection with up 1 spore of B. cereus in 25 g food sample. Using naturally contaminated food samples, standard method comforted the alternative method. In a number of cases, the alternative method was able to identify species not detected with the standard method. In addition, identification and discrimination between the B. cereus group members was possible. Thus, associated to a key element, i.e., the enrichment step, the developed multiparametric PCR-based assays reported in this study provide a fast, sensitive and reliable detection and identification tool for mostly encountered spore-forming food contaminants. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:78 / 88
页数:11
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