Chen Anqi, Wang Danhui, Nugen Sam R, Chen Juhong
Department of Food Science, Cornell University, Ithaca, NY 14853, USA.
Department of Food Science and Technology, The Ohio State University, Columbus, OH 43210, USA.
Microorganisms. 2021 Feb 19;9(2):436. doi: 10.3390/microorganisms9020436.
Despite enhanced sanitation implementations, foodborne bacterial pathogens still remain a major threat to public health and generate high costs for the food industry. Reporter bacteriophage (phage) systems have been regarded as a powerful technology for diagnostic assays for their extraordinary specificity to target cells and cost-effectiveness. Our study introduced an enzyme-based fluorescent assay for detecting the presence of using the T7 phage engineered with the operon which encodes beta-galactosidase (β-gal). Both endogenous and overexpressed β-gal expression was monitored using a fluorescent-based method with 4-methylumbelliferyl β-d-galactopyranoside (MUG) as the substrate. The infection of with engineered phages resulted in a detection limit of 10 CFU/mL in ground beef juice after 7 h of incubation. In this study, we demonstrated that the overexpression of β-gal coupled with a fluorogenic substrate can provide a straightforward and sensitive approach to detect the potential biological contamination in food samples. The results also suggested that this system can be applied to detect strains isolated from environmental samples, indicating a broader range of bacterial detection.
尽管卫生设施有所改善,但食源性病原体仍然是公共卫生的重大威胁,并给食品工业带来高昂成本。报告噬菌体系统因其对靶细胞具有非凡的特异性和成本效益,被视为诊断检测的一项强大技术。我们的研究引入了一种基于酶的荧光检测法,用于检测使用编码β-半乳糖苷酶(β-gal)的lac操纵子工程改造的T7噬菌体。以内源和过表达的β-gal为对象,使用以4-甲基伞形酮基β-D-吡喃半乳糖苷(MUG)为底物的荧光法进行监测。用工程噬菌体感染大肠杆菌,在孵育7小时后,在牛肉汁中的检测限为10 CFU/mL。在本研究中,我们证明β-gal的过表达与荧光底物相结合,可提供一种直接且灵敏的方法来检测食品样品中的潜在生物污染。结果还表明,该系统可用于检测从环境样品中分离出的大肠杆菌菌株,表明其细菌检测范围更广。