Björkroth K J, Korkeala H J
Department of Food and Environmental Hygiene, University of Helsinki, Finland.
Appl Environ Microbiol. 1997 Feb;63(2):448-53. doi: 10.1128/aem.63.2.448-453.1997.
Molecular typing was applied to an in-plant lactic acid bacterium (LAB) contamination analysis of a vacuum-packaged sliced cooked whole-meat product. A total of 982 LAB isolates from the raw mass, product, and the environment at different production stages were screened by restriction endonuclease (EcoRI and HindIII) analysis. rRNA gene restriction patterns were further determined for different strains obtained from each source. These patterns were used for recognizing the spoilage-causing LAB strains from the product on the sell-by day and tracing the sources and sites of spoilage LAB contamination during the manufacture. LAB typing resulted in 71 different ribotypes, of which 27 were associated with contamination routes. Raw material was distinguished as the source of the major spoilage strains. Contamination of the product surfaces after cooking was shown to be airborne. The removal of the product from the cooking forms was localized as a major site of airborne LAB contamination. Food handlers and some surfaces in contact with the product during the manufacture were also contaminated with the spoilage strains. Some LAB strains were also able to resist cooking in the core of the product bar. These strains may have an effect on the product shelf life by contaminating the slicing machine. The air in the slicing department and adjacent cold room contained very few LAB. Surface-mediated contamination was detected during the slicing and packaging stages. Food handlers also carried strains later found in the packaged product. Molecular typing provided useful information revealing the LAB contamination sources and sites of this product. The production line will be reorganized in accordance with these results to reduce spoilage LAB contamination.
分子分型技术被应用于对真空包装切片熟肉制品工厂内乳酸菌(LAB)污染情况的分析。通过限制性内切酶(EcoRI和HindIII)分析,对来自不同生产阶段的原料、产品及环境中的982株乳酸菌分离株进行了筛选。进一步确定了从每个来源获得的不同菌株的rRNA基因限制性图谱。这些图谱用于识别保质期内产品中导致变质的乳酸菌菌株,并追踪制造过程中变质乳酸菌污染的来源和部位。乳酸菌分型产生了71种不同的核糖型,其中27种与污染途径有关。原料被确定为主要变质菌株的来源。烹饪后产品表面的污染显示为空气传播。从烹饪模具中取出产品的位置被确定为空气传播乳酸菌污染的主要部位。食品处理人员以及制造过程中与产品接触的一些表面也被变质菌株污染。一些乳酸菌菌株也能够在产品棒的核心部位耐受烹饪。这些菌株可能通过污染切片机而影响产品的保质期。切片部门和相邻冷藏室中的空气中乳酸菌数量很少。在切片和包装阶段检测到表面介导的污染。食品处理人员也携带了后来在包装产品中发现的菌株。分子分型提供了有用信息,揭示了该产品中乳酸菌的污染来源和部位。将根据这些结果对生产线进行重组,以减少变质乳酸菌的污染。