ZIEL Institute for Food and Health, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 1, 85354, Freising, Germany.
Lehrstuhl für Mikrobielle Ökologie, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354, Freising, Germany.
Appl Microbiol Biotechnol. 2021 Feb;105(4):1693-1708. doi: 10.1007/s00253-021-11109-0. Epub 2021 Feb 1.
The heat-stable peptidase AprX, secreted by psychrotolerant Pseudomonas species in raw milk, is a major cause of destabilization and premature spoilage of ultra-high temperature (UHT) milk and milk products. To enable rapid detection and quantification of seven frequent and proteolytic Pseudomonas species (P. proteolytica, P. gessardii, P. lactis, P. fluorescens, P. protegens, P. lundensis, and P. fragi) in raw milk, we developed two triplex qPCR assays taking into account species-dependent differences in AprX activity. Besides five species-specific hydrolysis probes, targeting the aprX gene, a universal rpoB probe was included in the assay to determine the total Pseudomonas counts. For all six probes, linear regression lines between C value and target DNA concentration were obtained in singleplex as well as in multiplex approaches, yielding R values of > 0.975 and amplification efficiencies of 85-97%. Moreover, high specificity was determined using genomic DNA of 75 Pseudomonas strains, assigned to 57 species, and 40 other bacterial species as templates in the qPCR. Quantification of the target species and total Pseudomonas counts resulted in linear detection ranges of approx. 10-10 cfu/ml, which correspond well to common Pseudomonas counts in raw milk. Application of the assay using 60 raw milk samples from different dairies showed good agreement of total Pseudomonas counts calculated by qPCR with cell counts derived from cultivation. Furthermore, a remarkably high variability regarding the species composition was observed for each milk sample, whereby P. lundensis and P. proteolytica/P. gessardii were the predominant species detected. KEY POINTS: • Multiplex qPCR for quantification of seven proteolytic Pseudomonas species and total Pseudomonas counts in raw milk • High specificity and sensitivity via hydrolysis probes against aprX and rpoB • Rapid method to determine Pseudomonas contamination in raw milk and predict spoilage potential.
耐热肽酶 AprX 由嗜冷假单胞菌在生牛乳中分泌,是导致超高温(UHT)牛奶和乳制品不稳定和提前变质的主要原因。为了能够快速检测和定量生牛乳中七种常见且具有蛋白水解活性的假单胞菌(P. proteolytica、P. gessardii、P. lactis、P. fluorescens、P. protegens、P. lundensis 和 P. fragi),我们开发了两种三重 qPCR 检测方法,考虑到 AprX 活性的种间差异。除了针对 aprX 基因的五个种特异性水解探针外,该检测还包含一个通用的 rpoB 探针,用于确定总假单胞菌计数。对于所有六个探针,在单重和多重方法中均获得了 C 值与目标 DNA 浓度之间的线性回归线,得出的 R 值均大于 0.975,扩增效率为 85-97%。此外,使用 75 株假单胞菌属菌株的基因组 DNA(分为 57 种)和 40 种其他细菌种作为模板进行 qPCR 检测,结果显示具有高特异性。目标种和总假单胞菌计数的定量检测范围约为 10-10 cfu/ml,与生牛乳中常见的假单胞菌计数相吻合。使用来自不同乳品厂的 60 个生牛乳样品应用该检测方法,结果表明 qPCR 计算的总假单胞菌计数与培养法得出的细胞计数具有良好的一致性。此外,每个牛乳样品的种间组成差异显著,其中 P. lundensis 和 P. proteolytica/P. gessardii 是主要检测到的种群。关键点:• 用于定量检测生牛乳中七种蛋白水解假单胞菌和总假单胞菌计数的多重 qPCR• 针对 aprX 和 rpoB 的水解探针具有高特异性和灵敏度• 快速确定生牛乳污染并预测变质潜力的方法。