Simultaneous detection of pathogenic Listeria including atypical Listeria innocua in vegetables by a quadruplex PCR method

被引:14
|
作者
Rosimin, Aurelius Albert [1 ]
Kim, Min-Ju [1 ]
Joo, In-Sun [2 ]
Suh, Soo-Hwan [2 ]
Kim, Keun-Sung [1 ]
机构
[1] Chung Ang Univ, Dept Food Sci & Technol, Ansung 456756, Kyungki Do, South Korea
[2] Minist Food & Drug Safety, Food Microbiol Div, Cheongju 363700, Chungcheongbuk, South Korea
关键词
Quadruplex PCR; Pathogenic Listeria; Listeria monocytogenes; Listeria ivanovii; Atypical Listeria innocua; POLYMERASE-CHAIN-REACTION; MULTIPLEX PCR; IAP-GENE; MONOCYTOGENES; IDENTIFICATION; VIRULENCE; IVANOVII; FOOD; DIFFERENTIATION; PRODUCTS;
D O I
10.1016/j.lwt.2016.02.007
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Listeria species are major foodborne pathogens that are the causative agents of listeriosis, a severe infection with high fatality rates. The development of rapid methods to detect the potential presence of pathogenic Listeria is important, particularly in the food industry. In this study, we developed a quadruplex PCR method for simultaneous detection and differentiation of Listeria monocytogenes, Listeria ivanovii, Listeria innocua, and atypical L. innocua. The specificity of this PCR method was tested with 28 strains, including 15 Listeria strains and 13 other bacterial strains. The developed PCR method could detect target sequences in 0.1 ng/mu L of genomic DNA present in the reaction mixtures. By employing a combination of four primer pairs, all targeted Listeria species were successfully differentiated within a single reaction. Up to 1-10 CFU in 20 g green romaine vegetable samples could be detected after 24 h enrichment. The quadruplex PCR method developed in this study may be a useful alternative to culture based methods for the routine detection of Listeria in the food industry. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:601 / 607
页数:7
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