Olsen J E, Aabo S, Hill W, Notermans S, Wernars K, Granum P E, Popovic T, Rasmussen H N, Olsvik O
KVL - Centre for Food Research, Department of Veterinary Microbiology, The Royal Veterinary and Agricultural University, Frederiksberg C., Denmark.
Int J Food Microbiol. 1995 Nov;28(1):1-78. doi: 10.1016/0168-1605(94)00159-4.
DNA-hybridization and the polymerase chain reaction (PCR) are techniques commonly used to detect pathogenic bacteria. In this paper, the use of these techniques for detection of Salmonella, E. coli, V. cholerae, non-O1 Vibrio, Yersinia enterocolitica, Campylobacter, Listeria monocytogenes, Staphylococcus aureus, Bacillus cereus, Clostridium perfringens, and C. botulinum is reviewed with emphasis on application in food microbiology. In food control, DNA-techniques have most often been used in a 'culture confirmation' fashion, i.e. bacteria are enriched and sometimes even purified by traditional culture procedures and thereafter identified by the use of DNA-based methods. The most desirable approach is, however, to detect organisms directly in the food, but major problems remain to be solved before this can be routinely performed.
DNA杂交和聚合酶链反应(PCR)是常用于检测病原菌的技术。本文综述了这些技术在检测沙门氏菌、大肠杆菌、霍乱弧菌、非O1群弧菌、小肠结肠炎耶尔森菌、弯曲杆菌、单核细胞增生李斯特菌、金黄色葡萄球菌、蜡样芽孢杆菌、产气荚膜梭菌和肉毒梭菌中的应用,重点介绍了其在食品微生物学中的应用。在食品控制中,DNA技术最常以“培养物确认”的方式使用,即通过传统培养程序对细菌进行富集,有时甚至进行纯化,然后使用基于DNA的方法进行鉴定。然而,最理想的方法是直接在食品中检测微生物,但在能够常规进行之前,仍有一些主要问题有待解决。