RAPID DETECTION OF listeria monocytogenes IN FOOD BY POLYMERASE CHAIN REACTION

被引:1
作者
Ennaji, H. [1 ]
Timinouni, M. [2 ]
Ennaji, M. M. [3 ]
Ait, M'Hand R. [3 ]
Hassar, M. [3 ]
Cohen, N. [1 ]
机构
[1] Inst Pasteur Maroc 1, Lab Microbiol & Hyg Aliments & Environm, Casablanca 20100, Morocco
[2] Inst Pasteur 1, Lab Microbiol & Biol Mol, Casablanca 20100, Morocco
[3] Univ Hassan 2, Lab Virol Hyg & Microbiol, Fac Sci & Tech Mohammedia, Mohammadia 20650, Morocco
关键词
Cheese; Listeria monocytogenes; meats; milk; Polymerase Chain Reaction; PCR; MILK; INHIBITION; PRODUCTS; OUTBREAK; CELLS; SPP; GENE;
D O I
10.1170/126
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The standard conventional methods for the detection of Listeria monocytogenes in foods require high time 7 to 10 days to give ready results. To dissolve this problem we have evaluate a short method using Polymerase Chain Reaction (PCR) to analyze food samples. In parallel with this study, a comparison was made between PCR amplification from templates directly prepared from food and the official standard ISO procedure 11290-1. In this study we have used a Half Frazer broth as an enrichment medium; there were positive results of PCR detection of L. monocytogenes in different food sample analyzed (milk, cheese and meat) with approximately 1.5 10(1) Colony Forming Units /25g in less than 36 h. This PCR procedure has proved to be rapid and sensitive method suitable for the routine analysis; firstly, because this assay required just a short pre-enrichment step before PCR. Secondly, this procedure is very simple and time-saving; it could take less than one working day to obtain results if initial microbiological load was very important.
引用
收藏
页码:OL1104 / OL1110
页数:7
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