Screening of food raw materials for the presence of Shiga toxin-producing Escherichia coli O91:H21

被引:12
作者
Madic, J. [1 ,2 ]
Lecureuil, C. [1 ]
Dilasser, F. [1 ]
Derzelle, S. [1 ]
Jamet, E. [2 ]
Fach, P. [1 ]
Auvray, F. [1 ]
机构
[1] AFSSA LERQAP, F-94706 Maisons Alfort, France
[2] ACTILAIT, LEAMIL, La Roche Sur Foron, France
关键词
atypical EHEC; E; coli; O91:H21; real-time PCR; saa; STEC; stx; HEMOLYTIC-UREMIC SYNDROME; 5'-NUCLEASE PCR; SAA GENE; MOLECULAR CHARACTERIZATION; PUTATIVE ADHESINS; INTESTINAL MUCUS; STRAINS; VIRULENCE; IDENTIFICATION; VARIANTS;
D O I
10.1111/j.1472-765X.2008.02549.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To provide information on the prevalence and detection, in foods, of Shiga toxin-producing Escherichia coli (STEC) O91:H21. Seven hundred fifteen minced beef meats and 205 raw milk samples were analysed by stx-specific PCR-ELISA. Samples positive for stx were subsequently tested for the presence of wzy-O91, fliC-H21 and the adhesin-encoding gene saa. For minced meat, 16 (2.2%) and 11 (1.5%) samples were found positive for (stx, wzy-O91, fliC-H21) and (stx, wzy-O91, fliC-H21, saa) combinations, respectively. For raw milk, seven (3.4%) samples were found positive for the (stx, wzy-O91, fliC-H21) combination but none of these contained saa. Two STEC O91:H21 saa-positive strains and three STEC O91 H21- and saa-negative strains were isolated by colony hybridization. A low prevalence of potentially pathogenic STEC O91:H21 in food products was found using a combination of PCR assays targeting stx, wzy-O91, fliC-H21 and saa. The PCR-based approach described here represents a valuable method for rapid screening of food samples contaminated by STEC O91:H21.
引用
收藏
页码:447 / 451
页数:5
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