Cudjoe K S, Krona R
Department of Pharmacology, Microbiology and Food Hygiene, Norwegian College of Veterinary Medicine, Oslo, Norway.
Int J Food Microbiol. 1997 Jun 17;37(1):55-62. doi: 10.1016/s0168-1605(97)00050-0.
A Dynal core method has been established using Dynabeads anti-Salmonella to detect Salmonella from all categories of food samples. The protocol consists of the standard pre-enrichment of samples in buffered peptone water followed by immunomagnetic separation and subsequent selective enrichment of the bead-bacteria complexes in Rappaport-Vassiliadis Soya Peptone broth before plating onto Salmonella selective media. This modified IMS cultural method is intended to replace or augment traditional cultural methods used for Salmonella detection due to its specificity and increased sensitivity. The optional direct plating of bead-bacteria complexes onto solid media using a swab-streak technique is suitable for processed foods or samples known to have a history of very low resident flora. In an evaluation using 100 naturally contaminated samples, this IMS core method detected 39 of the 44 positive samples detected by all the methods combined, compared to 31 detected by the conventional ISO 6579 reference method. Furthermore, in ten different food matrices inoculated with low levels (1-5 cells/25 g) of twenty Salmonella serovariants, frozen for one month before being examined, the IMS core method, showed a 90% concordance with the ISO method and isolated two more Salmonella positive samples than the conventional ISO method.
已建立一种使用抗沙门氏菌 Dynabeads 的 Dynal 核心方法,用于从各类食品样本中检测沙门氏菌。该方案包括在缓冲蛋白胨水中对样本进行标准预富集,随后进行免疫磁分离,以及在将珠-菌复合物接种到沙门氏菌选择性培养基上之前,在 Rappaport-Vassiliadis 大豆蛋白胨肉汤中对其进行后续选择性富集。这种改良的免疫磁分离培养方法因其特异性和更高的灵敏度,旨在替代或补充用于沙门氏菌检测的传统培养方法。使用拭子划线技术将珠-菌复合物直接接种到固体培养基上这一可选方法,适用于加工食品或已知本地菌群数量极低的样本。在一项对 100 个自然污染样本的评估中,与传统 ISO 6579 参考方法检测出的 31 个阳性样本相比,这种免疫磁分离核心方法检测出了所有方法联合检测出的 44 个阳性样本中的 39 个。此外,在接种了低水平(1 - 5 个细胞/25 g)的二十种沙门氏菌血清型、在检测前冷冻一个月的十种不同食品基质中,免疫磁分离核心方法与 ISO 方法的一致性为 90%,并且比传统 ISO 方法多分离出两个沙门氏菌阳性样本。