Chan S W, Wilson S G, Vera-Garcia M, Whippie K, Ottaviani M, Whilby A, Shah A, Johnson A, Mozola M A, Halbert D N
Gene-Trak Systems, Framingham, MA 01701.
J Assoc Off Anal Chem. 1990 May-Jun;73(3):419-24.
A second generation nucleic acid hybridization assay has been developed and evaluated against the conventional culture method for detection of salmonellae in foods. The assay involves a liquid hybridization with Salmonella-specific oligonucleotide probes, capture of probe:target hybrids onto a solid support (plastic dipstick), and a colorimetric end point detection. The assay can be completed in 2.5 h, following approximately 44 h of culture enrichment. One thousand samples representing 20 food types were analyzed in parallel by both methods. Samples included uninoculated test product, and product inoculated with Salmonella at 2 levels. Eighteen Salmonella serotypes were used as inocula. The data demonstrate that the colorimetric hybridization method and the conventional culture method are equivalent in their ability to detect Salmonella contamination of foods.
已开发出一种第二代核酸杂交检测方法,并与传统培养方法进行了比较,以检测食品中的沙门氏菌。该检测方法包括与沙门氏菌特异性寡核苷酸探针进行液相杂交,将探针:靶标杂交体捕获到固体支持物(塑料试纸条)上,以及比色终点检测。在大约44小时的培养富集后,该检测方法可在2.5小时内完成。两种方法同时对代表20种食品类型的1000个样品进行了分析。样品包括未接种的测试产品,以及接种了两种水平沙门氏菌的产品。使用了18种沙门氏菌血清型作为接种物。数据表明,比色杂交法和传统培养法在检测食品中沙门氏菌污染的能力方面相当。