Ye Jianming, Guo Jiaqing, Li Tairan, Tian Jiaxin, Yu Mengxi, Wang Xiaochen, Majeed Usman, Song Wei, Xiao Jianbo, Luo Yane, Yue Tianli
College of Food Science and Technology, Northwest University, Xi'an, Shaanxi, China.
Department of Analytical Chemistry and Food Science, Faculty of Food Science and Technology, University of Vigo-Ourense Campus, Ourense, Spain.
Compr Rev Food Sci Food Saf. 2022 Mar;21(2):1843-1867. doi: 10.1111/1541-4337.12908. Epub 2022 Feb 10.
Foodborne pathogens and microbial toxins are the main causes of foodborne illness. However, trace pathogens and toxins in foods are difficult to detect. Thus, techniques for their rapid and sensitive identification and quantification are urgently needed. Phages can specifically recognize and adhere to certain species of microbes or toxins due to molecular complementation between capsid proteins of phages and receptors on the host cell wall or toxins, and thus they have been successfully developed into a detection platform for pathogens and toxins. This review presents an update on phage-based luminescent detection technologies as well as their working principles and characteristics. Based on phage display techniques of temperate phages, reporter gene detection assays have been designed to sensitively detect trace pathogens by luminous intensity. By the host-specific lytic effects of virulent phages, enzyme-catalyzed chemiluminescent detection technologies for pathogens have been exploited. Notably, these phage-based luminescent detection technologies can discriminate viable versus dead microbes. Further, highly selective and sensitive immune-based assays have been developed to detect trace toxins qualitatively and quantitatively via antibody analogs displayed by phages, such as phage-ELISA (enzyme-linked immunosorbent assay) and phage-IPCR (immuno-polymerase chain reaction). This literature research may lead to novel and innocuous phage-based rapid detection technologies to ensure food safety.
食源性病原体和微生物毒素是食源性疾病的主要病因。然而,食品中的痕量病原体和毒素难以检测。因此,迫切需要能够对它们进行快速、灵敏鉴定和定量的技术。由于噬菌体的衣壳蛋白与宿主细胞壁上的受体或毒素之间存在分子互补,噬菌体能够特异性识别并附着于某些种类的微生物或毒素,因此它们已被成功开发成为一种病原体和毒素的检测平台。本文综述了基于噬菌体的发光检测技术及其工作原理和特点。基于温和噬菌体的噬菌体展示技术,设计了报告基因检测方法,通过发光强度灵敏地检测痕量病原体。利用烈性噬菌体的宿主特异性裂解作用,开发了病原体的酶催化化学发光检测技术。值得注意的是,这些基于噬菌体的发光检测技术能够区分活微生物和死微生物。此外,还开发了高选择性和灵敏性的免疫检测方法,通过噬菌体展示的抗体类似物对痕量毒素进行定性和定量检测,如噬菌体酶联免疫吸附测定(ELISA)和噬菌体免疫聚合酶链反应(IPCR)。该文献研究可能会催生新型、无害的基于噬菌体的快速检测技术,以确保食品安全。