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Monitoring Biofilm Formation and Microbial Interactions that May Occur During a Salmonella Contamination Incident across the Network of a Water Bottling Plant

机译:监测整个灌装厂网络中沙门氏菌污染事件中可能发生的生物膜形成和微生物相互作用

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摘要

The present study aims to monitor the ability of Salmonella to colonize and compete as a member of the mixed species biofilm within key points at a water bottling plant, in case of a contamination incident with this major foodborne pathogen. To achieve this goal, bacterial communities throughout the production line were collected and their identities were investigated by microbial counts and polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE). These bacterial communities alone or along with constructed Salmonella enterica serovar Typhimurium (ST) fluorescence-based bioreporters were left to form a biofilm on stainless steel for 6 days at 20 °C. ST bioreporters were constructed by introducing plasmids expressing EYFP (enhanced yellow fluorescent protein) fusions of the genes csgB, csrA, sspH2, and fliD into ST 14028S. The bead vortexing-plate counting method was applied for the enumeration of the biofilm population, while the behavior of the bioreporters was evaluated by fluorescence microscopy. From a set of 16 samples that were collected from the plant, species of Citrobacter, Staphylococcus, Pseudomonas, Bacillus, and Exiguobacterium were identified. The presence of these indigenous bacteria neither inhibited nor enhanced the biofilm formation of ST in mixed bacterial communities (p > 0.05). Furthermore, the csrA-based bioreporter was shown to be induced in multispecies biofilms with Citrobacter. In conclusion, this study enhanced our knowledge of bacterial interactions occurring within a biofilm in a water bottling plant.
机译:本研究旨在监测沙门氏菌在水装瓶厂关键点内定殖并作为混合物种生物膜成员竞争的能力,以防这种主要食源性病原体发生污染事件。为了实现这一目标,收集了整个生产线中的细菌群落,并通过微生物计数和聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)对其身份进行了研究。这些细菌群落单独或与已构建的肠炎沙门氏菌血清型鼠伤寒(ST)荧光生物报告一起在20°C下在不锈钢上形成生物膜6天。通过将表达csFPB,csrA,sspH2和fliD基因的EYFP(增强型黄色荧光蛋白)融合体的质粒导入ST 14028S,构建ST生物报道基因。珠涡旋板计数法用于生物膜种群的计数,而生物报告者的行为通过荧光显微镜评估。从植物中收集的一组16个样品中,鉴定出柠檬酸杆菌,葡萄球菌,假单胞菌,芽孢杆菌和Exiguobacterium的物种。这些本地细菌的存在既没有抑制也没有增强混合细菌群落中ST的生物膜形成(p> 0.05)。此外,已证明基于csrA的生物报道分子在柠檬酸杆菌的多物种生物膜中被诱导。总之,这项研究增强了我们对装瓶厂中生物膜内细菌相互作用的认识。

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