Abouelnaga M, Lamas A, Miranda J M, Osman M, Cepeda A, Franco C M
Department of Analytical Chemistry, Nutrition and Food Science, Faculty of Veterinary, University of Santiago de Compostela, Lugo 27002, Spain; Dairy Department, Faculty of Agriculture, Suez Canal University, Ismailia 41522, Egypt.
Department of Analytical Chemistry, Nutrition and Food Science, Faculty of Veterinary, University of Santiago de Compostela, Lugo 27002, Spain.
J Dairy Sci. 2016 Oct;99(10):7864-7871. doi: 10.3168/jds.2016-10852. Epub 2016 Aug 4.
In our study, a new and highly sensitive real-time PCR Taqman assay was developed for the direct and specific detection of Bacillus sporothermodurans in UHT milk. The target region was selected based on the 16S rRNA gene profiles of 11 B. sporothermodurans from GenBank. A standard curve was created using a reference strain of B. sporothermodurans, DSM 10599. A low limit of detection for B. sporothermodurans in UHT milk (10 cfu/mL) was obtained. Furthermore, a total of 110 UHT milk samples from several supermarkets were directly assessed to detect and quantify B. sporothermodurans using the real-time PCR Taqman developed. The B. sporothermodurans counts obtained were highly correlated with the microbial plate counts in the UHT milk samples. This is the first time that B. sporothermodurans has been quantified directly from UHT milk. This technique could be applicable as a routine tool for preventing the growth of these bacteria by allowing for the rapid screening of raw milk samples in dairy plants. As expected, the probability of bacterial growth in UHT milk packages increased with the B. sporothermodurans counts in the raw milk.
在我们的研究中,开发了一种新型且高度灵敏的实时荧光定量PCR Taqman检测方法,用于直接特异性检测超高温瞬时灭菌(UHT)牛奶中的嗜热栖热芽孢杆菌。基于来自GenBank的11株嗜热栖热芽孢杆菌的16S rRNA基因图谱选择目标区域。使用嗜热栖热芽孢杆菌参考菌株DSM 10599创建标准曲线。获得了超高温瞬时灭菌牛奶中嗜热栖热芽孢杆菌的低检测限(10 cfu/mL)。此外,直接评估了来自几家超市的总共110份超高温瞬时灭菌牛奶样品,使用所开发的实时荧光定量PCR Taqman方法检测和定量嗜热栖热芽孢杆菌。所获得的嗜热栖热芽孢杆菌计数与超高温瞬时灭菌牛奶样品中的微生物平板计数高度相关。这是首次直接从超高温瞬时灭菌牛奶中对嗜热栖热芽孢杆菌进行定量。该技术可作为一种常规工具,通过对乳品厂的原料奶样品进行快速筛查来防止这些细菌的生长。正如预期的那样,超高温瞬时灭菌牛奶包装中细菌生长的可能性随着原料奶中嗜热栖热芽孢杆菌的计数增加而增加。