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首页> 外文期刊>International Journal of Food Microbiology >Monitoring of bacterial load in terms of culturable and non-culturable cells on new materials placed in a delicatessen serve over counter.
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Monitoring of bacterial load in terms of culturable and non-culturable cells on new materials placed in a delicatessen serve over counter.

机译:根据放置在熟食店中的新材料上可培养和不可培养细胞的细菌负荷监测服务。

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摘要

The aim of this study was to determine how quickly the surface of a refrigerated supermarket serve over counter becomes loaded with bacteria. New material made of polyvinyl chloride or stainless steel was placed on the surface on which foodstuffs are displayed for sale. One to three samples per week for 7 weeks were collected on gauze pads. CFUs were counted and total cells were quantified by real-time PCR. "Viable" cells using real-time PCR following pre-treatment with ethidium monoazide were quantified on stainless steel. Attachment strengths were assessed at the end of the experiment by constructing detachment curves. Whatever the material, on day 1 the microbial load reached values near those observed in the following weeks i.e. 103-104 log total cells/cm2. The number of cells deposited in one week was compensated for by the small reduction obtained by cleaning and disinfection (C&D). The mean difference between total and viable cells was 0.54 log CFUs/cm2. A big drop in CFUs following C&D was observed at the beginning of the experiment, despite no visible decrease in the number of viable cells, but the CFU reduction decreased over time. Nevertheless, the low efficiency of C&D on the dominant microbiota did not indicate the fate of pathogenic bacteria on these materials. Our data suggest that dead cells do not adhere quite so well as viable cells. Although no growth was observed and the attached bacterial community cannot therefore be considered a biofilm, attached cells shared certain properties attributed to biofilms i.e. their resistance to C&D increased over time and they followed a biphasic detachment curve.
机译:这项研究的目的是确定冷藏超市柜台上服务的表面细菌装载的速度。将由聚氯乙烯或不锈钢制成的新材料放在要出售食品的表面上。在纱布垫上每周收集1至3个样品,共7周。对CFU进行计数,并通过实时PCR定量总细胞。在不锈钢上定量用单叠氮化乙锭预处理后使用实时PCR的“活”细胞。在实验结束时,通过构建脱离曲线评估附着强度。无论采用哪种材料,第一天的微生物负荷量都接近于随后几周观察到的数值,即10 3 -10 4 对数总细胞/ cm 2 。一周内沉积的细胞数量可通过清洁和消毒(C&D)的少量减少来补偿。总细胞与活细胞的平均差为0.54 log CFUs / cm 2 。在实验开始时,观察到了C&D之后CFU的大幅下降,尽管活细胞数量没有明显减少,但CFU的减少随时间而减少。然而,在优势菌群上进行C&D的效率低并不表明这些材料上病原菌的命运。我们的数据表明,死细胞不像活细胞那样好粘附。尽管未观察到生长,因此不能将附着的细菌群落视为生物膜,但附着的细胞具有某些归因于生物膜的特性,即其对C&D的抗性随时间增加,并且遵循双相分离曲线。

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