Istituto di Scienze dell'Alimentazione-CNR, 83100 Avellino, Italy.
Dipartimento di Scienze, Università degli Studi della Basilicata, 85100 Potenza, Italy.
Int J Food Microbiol. 2019 Mar 16;293:102-113. doi: 10.1016/j.ijfoodmicro.2019.01.008. Epub 2019 Jan 16.
Thawed hake (Merluccius capensis and M. paradoxus) and plaice (Pleuronectes platessa) fillets were used as a model to evaluate the effect of storage temperature (0 or 10 °C) and biological variability (fish species, lot to lot) on bacterial growth kinetics and microbial successions. Both culture dependent methods (plate counts on non-selective and selective media) and culture independent methods (qPCR and 16S rRNA gene metabarcoding) were used. Bacterial counts exceeded 10 cfu/g within 2-3 days at 10 °C and 7-8 days at 0 °C. Plate counts on three media (Plate Count Agar +0.5% NaCl, Iron Agar Lyngby and Pseudomonas Selective medium) and 16S rRNA gene counts estimated by qPCR were highly correlated. Growth was modelled using the D-model and specific growth rate ranged between 0.97 and 1.24 d and 3.54 and 5.90 d at 0 and 10 °C, respectively. The initial composition of the microbiota showed lot-to-lot variation, but significant differences between the two fish species were detected. Alpha diversity significantly decreased during storage. When bacterial counts exceeded 10 cfu/g, the microbiota was dominated by members of the genera Pseudomonas, Psychrobacter, Acinetobacter, Serratia, Flavobacterium, Acinetobacter, Carnobacterium, Brochothrix and Vagococcus. However, Photobacterium and Shewanella, two genera frequently associated with fish spoilage, were either absent or minor components of the microbiota. As expected, storage temperature significantly affected the abundance of several species. The inference of microbial association networks with three different approaches (an ensemble approach using the CoNet app, Sparse Correlations for Compositional data, and SParse InversE Covariance Estimation for Ecological Association Inference) allowed the detection of both a core microbiota, which was present throughout storage, and a number of taxa, which became dominant at the end of spoilage and were characterized by a disproportionate amount of negative interactions.
解冻的黑线鳕(Merluccius capensis 和 M. paradoxus)和欧鲽(Pleuronectes platessa)鱼片被用作模型,以评估储存温度(0 或 10°C)和生物变异性(鱼类物种、批次间)对细菌生长动力学和微生物演替的影响。使用了依赖培养的方法(非选择性和选择性培养基上的平板计数)和非依赖培养的方法(qPCR 和 16S rRNA 基因代谢组学)。在 10°C 下,细菌计数在 2-3 天内超过 10cfu/g,在 0°C 下,细菌计数在 7-8 天内超过 10cfu/g。三种培养基(普通琼脂+0.5%NaCl、铁琼脂 Lyngby 和假单胞菌选择性培养基)上的平板计数和 qPCR 估计的 16S rRNA 基因计数高度相关。使用 D 模型对生长进行建模,在 0 和 10°C 下,特定生长率分别在 0.97 和 1.24d 至 3.54 和 5.90d 之间。微生物群的初始组成显示出批次间的差异,但在两种鱼类之间检测到显著差异。在储存过程中,α多样性显著下降。当细菌计数超过 10cfu/g 时,微生物群由假单胞菌属、嗜冷菌属、不动杆菌属、沙雷氏菌属、黄杆菌属、不动杆菌属、食球菌属、布鲁氏菌属和魏斯氏菌属的成员主导。然而,与鱼类腐败经常相关的两个属 Photobacterium 和 Shewanella 要么不存在,要么是微生物群的次要成分。正如预期的那样,储存温度显著影响了几种物种的丰度。使用三种不同方法(使用 CoNet 应用程序的集合方法、用于组合数据的稀疏相关性和用于生态关联推断的稀疏逆协方差估计)推断微生物关联网络,不仅可以检测到存在于整个储存过程中的核心微生物群,还可以检测到一些在腐败末期占主导地位的分类群,它们的特征是存在大量的负相互作用。