de Cesare A, Manfreda G, Macrì M, Cantoni C
Department of Food Science, Alma Mater Studiorum, University of Bologna, Via S. Giacomo 9, 40126 Bologna, Italy.
J Food Prot. 2007 May;70(5):1116-21. doi: 10.4315/0362-028x-70.5.1116.
In March 2005, Listeria monocytogenes was detected on the rinds of Taleggio cheeses produced in an Italian plant. To identify the pathogen source, 154 rinds of cheeses that had been manually and automatically salinated and 52 environmental swabs collected from salting equipment, ripening cloths, and ripening boxes were tested for L. monocytogenes. Twenty-seven strains isolated from cheese samples and 16 strains isolated from environmental samples were genotyped by EcoRI and PvuII automated ribotyping. The microbiological results revealed a significant incidence of contamination of cheeses that were automatically salinated and contamination on the salting equipment, ripening cloths, and boxes. All cheese and environmental strains had the same EcoRI and PvuII ribotyping profiles, designated 153-204-S5 and 153-210-S-2, respectively. The only exception were three Taleggio strains, isolated from the same lot of product, that had EcoRI and PvuII ribotyping profiles designated 153-289-S6 and 153-214-S-5, respectively. Strains with EcoRI profile 153-204-S5 were classified as DUP-ID 1045 and serotype 1/2a, whereas strains with EcoRI profile 153-289-S6 were classified as DUP-ID 1034 and serotype 1/2b. The microbiological and molecular typing data collected in this study suggest that the source of the L. monocytogenes contamination in the Taleggio plant under study was the automated salting equipment. The isolate DUP-IDs were used to trace the introduction of potentially dangerous strains, such as those characterized as DUP-ID 1034, in the processing plant.
2005年3月,在一家意大利工厂生产的塔莱吉奥奶酪的外皮上检测到了单核细胞增生李斯特菌。为了确定病原体来源,对154个经人工和自动腌制的奶酪外皮以及从腌制设备、成熟布和成熟箱收集的52份环境拭子进行了单核细胞增生李斯特菌检测。从奶酪样品中分离出的27株菌株和从环境样品中分离出的16株菌株通过EcoRI和PvuII自动核糖体分型进行基因分型。微生物学结果显示,自动腌制的奶酪污染发生率很高,腌制设备、成熟布和箱子也受到了污染。所有奶酪和环境菌株具有相同的EcoRI和PvuII核糖体分型图谱,分别指定为153-204-S5和153-210-S-2。唯一的例外是从同一批次产品中分离出的三株塔莱吉奥菌株,其EcoRI和PvuII核糖体分型图谱分别指定为153-289-S6和153-214-S-5。具有EcoRI图谱153-204-S5的菌株被分类为DUP-ID 1045和血清型1/2a,而具有EcoRI图谱153-289-S6的菌株被分类为DUP-ID 1034和血清型1/2b。本研究收集的微生物学和分子分型数据表明,所研究的塔莱吉奥工厂中单核细胞增生李斯特菌污染的来源是自动腌制设备。分离出的DUP-IDs用于追踪加工厂中潜在危险菌株的引入,例如那些被鉴定为DUP-ID 1034的菌株。