Hoben D A, Ashton D H, Peterson A C
Appl Microbiol. 1973 Jan;25(1):123-9. doi: 10.1128/am.25.1.123-129.1973.
A rapid detection procedure was developed in which a lysine-iron-cystine-neutral red (LICNR) broth medium, originally described by Hargrove et al. in 1971, was modified and used to detect the presence of viable Salmonella organisms in a variety of foods, food ingredients, and feed materials by using a two-step enrichment technique. Tetrathionate broth was used to enrich samples with incubation at 41 C for 20 hr, followed by transfer to LICNR broth and incubation at 37 C for 24 hr for further enrichment and for the detection of Salmonella organisms by color change. One hundred ten samples representing 18 different sample types were evaluated for the presence of viable Salmonella. Ninety-four percent of the samples found to be presumptive positive by this method were confirmed as positive by a culture method. Fluorescent-antibody results also compared closely. A second study was conducted under quality-control laboratory conditions by using procedures currently employed for Salmonella detection. One hundred forty-three samples representing 19 different sample types were evaluated for the presence of viable Salmonella. No false negatives were observed with the rapid-detection method. The usefulness of the LICNR broth procedure as a screening technique to eliminate negative samples rapidly and to identify presumptive positive samples for the presence of viable Salmonella organisms was established in this laboratory.
开发了一种快速检测程序,其中对1971年由哈格罗夫等人最初描述的赖氨酸-铁-胱氨酸-中性红(LICNR)肉汤培养基进行了改良,并通过两步富集技术用于检测各种食品、食品成分和饲料原料中活的沙门氏菌。用四硫磺酸盐肉汤在41℃下培养20小时来富集样品,随后转移至LICNR肉汤中并在37℃下培养24小时以进一步富集并通过颜色变化检测沙门氏菌。对代表18种不同样品类型的110个样品进行了活沙门氏菌的检测评估。通过该方法初步判定为阳性的样品中,94%经培养法确认为阳性。荧光抗体检测结果也与之相近。在质量控制实验室条件下采用目前用于沙门氏菌检测的程序进行了第二项研究。对代表19种不同样品类型的143个样品进行了活沙门氏菌的检测评估。快速检测方法未出现假阴性结果。本实验室证实了LICNR肉汤程序作为一种筛选技术在快速排除阴性样品以及识别可能含有活沙门氏菌的初步阳性样品方面的有效性。