Ferrocino Ilario, Greppi Anna, La Storia Antonietta, Rantsiou Kalliopi, Ercolini Danilo, Cocolin Luca
Department of Agricultural, Forest and Food Science, University of Turin, Grugliasco, Italy.
Department of Agricultural Sciences, Division of Microbiology, University of Naples Federico II, Portici, Italy.
Appl Environ Microbiol. 2015 Nov 6;82(2):549-59. doi: 10.1128/AEM.03093-15. Print 2016 Jan 15.
Beef burgers were stored at 4°C in a vacuum in nisin-activated antimicrobial packaging. Microbial ecology analyses were performed on samples collected between days 0 and 21 of storage to discover the population diversity. Two batches were analyzed using RNA-based denaturing gradient gel electrophoresis (DGGE) and pyrosequencing. The active packaging retarded the growth of the total viable bacteria and lactic acid bacteria. Culture-independent analysis by pyrosequencing of RNA extracted directly from meat showed that Photobacterium phosphoreum, Lactococcus piscium, Lactobacillus sakei, and Leuconostoc carnosum were the major operational taxonomic units (OTUs) shared between control and treated samples. Beta diversity analysis of the 16S rRNA sequence data and RNA-DGGE showed a clear separation between two batches based on the microbiota. Control samples from batch B showed a significant high abundance of some taxa sensitive to nisin, such as Kocuria rhizophila, Staphylococcus xylosus, Leuconostoc carnosum, and Carnobacterium divergens, compared to control samples from batch A. However, only from batch B was it possible to find a significant difference between controls and treated samples during storage due to the active packaging. Predicted metagenomes confirmed differences between the two batches and indicated that the use of nisin-based antimicrobial packaging can determine a reduction in the abundance of specific metabolic pathways related to spoilage. The present study aimed to assess the viable bacterial communities in beef burgers stored in nisin-based antimicrobial packaging, and it highlights the efficacy of this strategy to prolong beef burger shelf life.
牛肉汉堡在4°C真空条件下保存在经乳链菌肽激活的抗菌包装中。对储存0至21天期间采集的样本进行微生物生态学分析,以发现种群多样性。使用基于RNA的变性梯度凝胶电泳(DGGE)和焦磷酸测序对两批样本进行分析。活性包装抑制了总活菌和乳酸菌的生长。通过对焦磷酸测序直接从肉中提取的RNA进行非培养分析表明,磷发光杆菌、嗜鱼乳球菌、清酒乳杆菌和肉囊乳杆菌是对照样品和处理样品之间共有的主要操作分类单元(OTU)。基于微生物群的16S rRNA序列数据和RNA-DGGE的β多样性分析显示两批样本之间有明显区分。与A批对照样品相比,B批对照样品中一些对乳链菌肽敏感的分类群,如嗜根考克氏菌、木糖葡萄球菌、肉囊乳杆菌和分歧肉杆菌,丰度显著较高。然而,由于活性包装,仅在B批中发现储存期间对照样品和处理样品之间存在显著差异。预测的宏基因组证实了两批样本之间的差异,并表明使用基于乳链菌肽的抗菌包装可以减少与腐败相关的特定代谢途径的丰度。本研究旨在评估储存在基于乳链菌肽的抗菌包装中的牛肉汉堡中的活菌群落,并强调该策略延长牛肉汉堡保质期的功效。