Simultaneous quantitative detection of Listeria spp. and Listeria monocytogenes using a duplex real-time PCR-based assay

被引:2
作者
Rodríguez-Lázaro, D
Hernández, M
Pla, M [1 ]
机构
[1] Univ Girona, Inst Food & Agr Technol, INTEA, E-17071 Girona, Spain
[2] CSIC, Inst Mol Biol, IBMB, E-08034 Barcelona, Spain
关键词
Listeria spp; Listeria monocytogenes; real-time PCR; multiplex; food-borne pathogen detection;
D O I
10.1016/j.femsle.2004.02.018
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report a duplex real-time PCR-based assay for the simultaneous quantitative detection of Lisieria spp. and the food-borne pathogen Listeria monocytogenes. The targets of this single tube reaction were the 23S rDNA and hly genes of Listeria spp. and L. monocytogenes, respectively. Our assay was efficient, 100% selective (i.e., it allowed accurate simultaneous identification of 52 L. monocytogenes and 120 Lisieria spp. strains through the FAM-labelled hly and the VIC-labelled 23S rDNA probes, respectively); and had a detection limit of one target molecule in 100% (23S rDNA) and 56% (hly) of the reactions. Simultaneous quantification was possible along a 5-log dynamic range, with an upper limit of 30 target molecules and R-2 values > 0.995 in both cases. Our results indicate that this assay based on the amplification of the 23S rDNA gene can accurately quantify any mixture of Listeria species and simultaneously unambiguously quantify L. monocytogenes. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 267
页数:11
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