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Identification and metagenetic characterisation of Listeria monocytogenes-harbouring communities present in food-related industrial environments

机译:食品相关工业环境中李斯特菌单核细胞植物的鉴定和鉴定性表征

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The main aim of this study was to localise, identify and characterise the Listeria monocytogenes-harbouring bacterial communities present in food related premises via 16S rRNA gene metagenetic analysis. With this scope, 319 environmental samples coming from a wide variety of surfaces of fish (n = 120), meat (n = 80) and dairy industries (n = 119), were firstly analysed following ISO 11290-1 and ISO 11290-2 norms. Direct L. monocytogenes quantification was possible in 9 samples (2.8%) with values between 2.00 and 3.97 log CFU/cm(2). After enrichment, an overall L. monocytogenes incidence of 12.54% (n = 40) was obtained, being samples from meat industry the most contaminated. Molecular serotyping assays showed that most of the isolates belonged to 1/2b-3b-7 subgroup, followed by 1/2a-3a and 1/2c-3c. These results combined with Ascl and ApaI PFGE macro-restriction patterns, yielded 7 different L. monocytogenes clusters. Nevertheless, no clear ecological relationships could be stablished. High amounts of L. monocytogenes-associated psychrotrophic microbiota were obtained in all cases with values above 9 log CFU/cm(2) in some cases. Metagenetic analysis of one representative sample per each food industry type (fish, meat, dairy) demonstrated that Actinobacteria (53.16%) was mostly present in the meat sample whereas Proteobacteria was the most representative phylum in dairy (69.58%) and fish (97.11%) samples. Subsequent operational taxonomic units (OTUs) analysis, showed a wide variety of taxa associated with L. monocytogenes such as spoilage-associated genera (e.g. Psyschromonas or Shewanella), lactic acid bacteria genera (e.g. Lactococcus or Lactobacillus) or pathogenic species such as Yersinia enterocolitica. It was thus demonstrated, that L. monocytogenes is capable to both survive with different bacteria in different ecological niches, highlighting once more the need for proper surveillance schedules so as to guarantee the safety of the food products.
机译:本研究的主要目的是通过16S rRNA基因分析分析定位,鉴定和表征储存中储存的细菌社区的李斯特里亚单核细胞植物。通过此范围,从鱼(n = 120),肉(n = 80)和乳制品(n = 119)之后,319个环境样本首先在ISO 11290-1和ISO 11290-2中分析了肉(n = 80)和乳制品(n = 119)规范。直接L.单核细胞增生定量在9个样品(2.8%)中,值为2.00和3.97 Log CFU / cm(2)。在富集后,获得了总体核细胞质的发病率为12.54%(n = 40),是来自肉行业最污染的样品。分子血清型测定结果表明,大多数分离株属于1 / 2B-3B-7亚组,其次是1 / 2A-3A和1 / 2C-3C。这些结果与ASCL和Apai PFGE宏观限制性模式相结合,得到7种不同的L.单核细胞元簇。然而,没有明确的生态关系可以稳定。在某些情况下,在所有情况下,在所有情况下获得高量的L.单核细胞生成的心理营养微生物群。每种食品工业类型(鱼类,肉类,乳制品)的一个代表性样品的Metagenetic分析表明,肉毒菌(53.16%)大多存在于肉类样品中,而乳菌是乳制品(69.58%)和鱼类中最代表性的球菌(97.11%) )样品。随后的运作分类单位(OTUS)分析显示,与L.单核细胞生成的诸如腐败相关的属(例如Psyschromonas或Shewanella),乳酸菌属(例如乳酸乳杆菌或乳酸杆菌)或致病性物种如yersinia肠菌等。因此证明,L.单核细胞增生能够在不同生态利基中与不同的细菌一起存活,突出更多需要适当的监测时间表,以保证食品的安全性。

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