Loncarevic S, Jørgensen H J, Løvseth A, Mathisen T, Rørvik L M
Section for Feed and Food Microbiology, National Veterinary Institute, The Norwegian School of Veterinary Science, Oslo, Norway.
J Appl Microbiol. 2005;98(2):344-50. doi: 10.1111/j.1365-2672.2004.02467.x.
To find out if testing of up to 10 Staphylococcus aureus isolates from each sample from raw milk and raw milk products for staphylococcal enterotoxin (SE) might increase the chances of identifying potential sources of food intoxication.
Altogether 386 S. aureus isolates were tested for the presence of SE by reversed passive latex agglutination (SET-RPLA), and SE genes (se) by a multiplex polymerase chain reaction (PCR). In 18 of 34 (53%) S. aureus positive samples a mixture of SE and/or se positive and negative isolates were identified. Multiplex PCR increased the number of potential SE producing strains, i.e. isolates that harboured se, with 51% among the product and 48% among the raw bovine milk isolates. Examination by pulsed-field gel electrophoresis mostly confirmed clonal similarity among isolates sharing SE/se profile, but did not further differentiate between them.
Isolates of S. aureus collected from one sample may show great diversity in SE production and different plating media seem to suppress or favour different strains of S. aureus.
Several isolates of S. aureus from each sample should be tested for enterotoxin production in cases with typical SE intoxication symptoms with methods that are able to reveal new SE/se.
探究对生乳及乳制品的每个样本中多达10株金黄色葡萄球菌分离株进行葡萄球菌肠毒素(SE)检测是否能增加识别食物中毒潜在源头的几率。
采用反向被动乳胶凝集试验(SET-RPLA)对总共386株金黄色葡萄球菌分离株进行SE检测,并通过多重聚合酶链反应(PCR)检测SE基因(se)。在34份(53%)金黄色葡萄球菌阳性样本中的18份中,鉴定出SE和/或se阳性及阴性分离株的混合物。多重PCR增加了潜在产SE菌株的数量,即在产品分离株中增加了51%,在生牛乳分离株中增加了48%,即携带se的分离株。脉冲场凝胶电泳检测大多证实了具有相同SE/se谱型的分离株之间的克隆相似性,但未进一步区分它们。
从一个样本中收集的金黄色葡萄球菌分离株在SE产生方面可能表现出很大差异,不同的平板培养基似乎会抑制或有利于不同菌株的金黄色葡萄球菌生长。
对于出现典型SE中毒症状的病例,应采用能够检测出新的SE/se的方法,对每个样本中的几株金黄色葡萄球菌分离株进行肠毒素产生检测。