Fantasia L D
Appl Microbiol. 1969 Nov;18(5):708-13. doi: 10.1128/am.18.5.708-713.1969.
An accelerated, direct immunofluorescent-antibody procedure was developed for the detection of Salmonella in food products. This method includes pre-enrichment and selective enrichment but eliminates many of the washing and smear treatments present in existing methods. Commercially available fluorescein-conjugated somatic antiserum was used in comparing this method with conventional culture, biochemical, and serological procedures. The 894 samples tested represented 39 different products. The fluorescent-antibody procedure detected Salmonella in 216 test samples as compared to 205 positives recovered by using the standard culture procedures. In no instance did the fluorescent-antibody procedure fail to detect a Salmonella positive which had been detected by the standard procedure. With a three-tube, most-probable-number procedure, the fluorescent-antibody method was able to detect Salmonella at a level of 0.036 organism per g. In addition to being a more rapid method for the detection of Salmonella, it has proven to be comparable to conventional culture procedures.
开发了一种用于检测食品中沙门氏菌的加速直接免疫荧光抗体程序。该方法包括预富集和选择性富集,但省去了现有方法中的许多洗涤和涂片处理。使用市售的荧光素偶联菌体抗血清将该方法与传统的培养、生化和血清学程序进行比较。所检测的894个样品代表39种不同产品。荧光抗体程序在216个测试样品中检测到沙门氏菌,而使用标准培养程序回收了205个阳性样品。荧光抗体程序从未未能检测到标准程序检测出的沙门氏菌阳性样品。采用三管最大可能数法,荧光抗体法能够检测到每克0.036个菌体水平的沙门氏菌。除了是一种检测沙门氏菌的更快方法外,它已被证明与传统培养程序相当。