Analytical opportunities of quantitative polymerase chain reaction in dairy microbiology

被引:23
作者
Boyer, Mickael [1 ]
Combrisson, Jerome [1 ]
机构
[1] Danone Res, Ctr Daniel Carasso, RD 128, F-91700 Palaiseau, France
关键词
REAL-TIME PCR; LISTERIA-MONOCYTOGENES CELLS; ESCHERICHIA-COLI O157; GENE-BASED PRIMERS; 16S RIBOSOMAL-RNA; PROPIDIUM MONOAZIDE; ETHIDIUM MONOAZIDE; SALMONELLA SPP; BIFIDOBACTERIUM-LONGUM; FERMENTED MILK;
D O I
10.1016/j.idairyj.2012.11.008
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Recent developments in molecular methods aid in detecting and quantifying food microorganisms through faster, more sensitive and more specific procedures than classical microbiology techniques. Molecular tools were widely used to detect pathogens in food but yet remain insufficient to directly quantify them in food products. Nevertheless, recent studies show that quantitative PCR (qPCR)-based methods are applied with success in enumerating fermenting microbes and health promoting bacteria in dairy products. The increasing number of sequenced genomes is now a crucial support to designing specific primers and probes. Technological advances in qPCR-based methods including viable quantitative PCR are also highlighted and could be promising strategies for quantifying merely viable cells, detecting multiple microorganisms in a single reaction and constructing high throughput PCR work-flows. Application of real-time PCR in the food industry has proven its reliability nevertheless its widespread use in the dairy industry will need technical recommendations and standardisation methods. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:45 / 52
页数:8
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