Cauchie Emilie, Delhalle Laurent, Taminiau Bernard, Tahiri Assia, Korsak Nicolas, Burteau Sophie, Fall Papa Abdoulaye, Farnir Frédéric, Baré Ghislain, Daube Georges
Department of Food Sciences, Fundamental and Applied Research for Animals & Health (FARAH), Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.
Quality Partner sa, Liège, Belgium.
Front Microbiol. 2020 Jan 21;10:3074. doi: 10.3389/fmicb.2019.03074. eCollection 2019.
Although several studies have focused on the dynamics of bacterial food community, little is known about the variability of batch production and microbial changes that occur during storage. The aim of the study was to characterize the microbial spoilage community of minced pork meat samples, among different food production and storage, using both 16S rRNA gene sequencing and classical microbiology. Three batches of samples were obtained from four local Belgian facilities (A-D) and stored until shelf life under food wrap (FW) and modified atmosphere packaging (MAP, CO 30%/O 70%), at constant and dynamic temperature. Analysis of 288 samples were performed by 16S rRNA gene sequencing in combination with counts of psychrotrophic and lactic acid bacteria at 22°C. At the first day of storage, different psychrotrophic counts were observed between the four food companies (Kruskal-Wallist test, -value < 0.05). Results shown that lowest microbial counts were observed at the first day for industries D and A (4.2 ± 0.4 and 5.6 ± 0.1 log CFU/g, respectively), whereas industries B and C showed the highest results (7.5 ± 0.4 and 7.2 ± 0.4 log CFU/g). At the end of the shelf life, psychrotrophic counts for all food companies was over 7.0 log CFU/g. With metagenetics, 48 OTUs were assigned. At the first day, the genus (86.7 and 19.9% for food industries A and C, respectively) and (38.7 and 25.7% for food companies B and D, respectively) were dominant. During the storage, a total of 12 dominant genera (>5% in relative abundance) were identified in MAP and 7 in FW. was more present in FW and this genus was potentially replaced by in MAP (two-sided Welch's -test, -value < 0.05). Also, a high Bray-Curtis dissimilarity in genus relative abundance was observed between food companies and batches. Although the bacteria consistently dominated the microbiota in our samples are known, results indicated that bacterial diversity needs to be addressed on the level of food companies, batches variation and food storage conditions. Present data illustrate that the combined approach provides complementary results on microbial dynamics in minced pork meat samples, considering batches and packaging variations.
尽管有几项研究聚焦于细菌食物群落的动态变化,但对于批量生产的变异性以及储存过程中发生的微生物变化却知之甚少。本研究的目的是利用16S rRNA基因测序和经典微生物学方法,对不同食品生产和储存条件下的碎猪肉样本的微生物腐败群落进行特征描述。从比利时当地的四个设施(A - D)获取了三批样本,并在保鲜膜(FW)和气调包装(MAP,CO₂ 30%/O₂ 70%)下,在恒定和动态温度下储存直至保质期结束。通过16S rRNA基因测序结合在22°C下对嗜冷菌和乳酸菌的计数,对288个样本进行了分析。在储存的第一天,四个食品公司之间观察到不同的嗜冷菌计数(Kruskal - Wallis检验,p值 < 0.05)。结果表明,D和A公司在第一天观察到的微生物计数最低(分别为4.2 ± 0.4和5.6 ± 0.1 log CFU/g),而B和C公司的结果最高(7.5 ± 0.4和7.2 ± 0.4 log CFU/g)。在保质期结束时,所有食品公司的嗜冷菌计数均超过7.0 log CFU/g。通过宏基因组学,确定了48个操作分类单元(OTU)。在第一天,A和C食品公司中 属(分别为86.7%和19.9%)以及B和D食品公司中 属(分别为38.7%和25.7%)占主导地位。在储存过程中,在MAP中总共鉴定出12个优势属(相对丰度>5%),在FW中鉴定出7个。 属在FW中更常见,并且该属在MAP中可能被 属取代(双侧Welch's t检验,p值 < 0.05)。此外,在食品公司和批次之间观察到属相对丰度的高Bray - Curtis差异。尽管已知在我们的样本中始终占主导地位的细菌菌群,但结果表明,需要在食品公司、批次差异和食品储存条件的层面上解决细菌多样性问题。目前的数据表明,考虑到批次和包装差异,这种联合方法为碎猪肉样本中的微生物动态提供了互补的结果。