Fricker Martina, Messelhäusser Ute, Busch Ulrich, Scherer Siegfried, Ehling-Schulz Monika
Abt. Mikrobiologie/ZIEL, TUM, Weihenstephaner Berg 3, 85354 Freising, Germany.
Appl Environ Microbiol. 2007 Mar;73(6):1892-8. doi: 10.1128/AEM.02219-06. Epub 2007 Jan 26.
Cereulide-producing Bacillus cereus can cause an emetic type of food-borne disease that mimics the symptoms provoked by Staphylococcus aureus. Based on the recently discovered genetic background for cereulide formation, a novel 5' nuclease (TaqMan) real-time PCR assay was developed to provide a rapid and sensitive method for the specific detection of emetic B. cereus in food. The TaqMan assay includes an internal amplification control and primers and a probe designed to target a highly specific part of the cereulide synthetase genes. Additionally, a specific SYBR green I assay was developed and extended to create a duplex SYBR green I assay for the one-step identification and discrimination of the two emesis-causing food pathogens B. cereus and S. aureus. The inclusivity and exclusivity of the assay were assessed using a panel of 100 strains, including 23 emetic B. cereus and 14 S. aureus strains. Different methods for DNA isolation from artificially contaminated foods were evaluated, and established real-time assays were used to analyze two recent emetic food poisonings in southern Germany. One of the food-borne outbreaks included 17 children visiting a day care center who vomited after consuming a reheated rice dish, collapsed, and were hospitalized; the other case concerned a single food-poisoning incident occurring after consumption of cauliflower. Within 2 h, the etiological agent of these food poisonings was identified as emetic B. cereus by using the real-time PCR assay.
产cereulide的蜡样芽孢杆菌可引起一种催吐型食源性疾病,其症状类似于由金黄色葡萄球菌引发的症状。基于最近发现的cereulide形成的遗传背景,开发了一种新型5'核酸酶(TaqMan)实时荧光定量PCR检测方法,为食品中催吐型蜡样芽孢杆菌的特异性检测提供一种快速且灵敏的方法。TaqMan检测方法包括一个内部扩增对照以及设计用于靶向cereulide合成酶基因高度特异性区域的引物和探针。此外,还开发并扩展了一种特异性SYBR Green I检测方法,以创建一种双链SYBR Green I检测方法,用于一步鉴定和区分两种导致呕吐的食源性病原体蜡样芽孢杆菌和金黄色葡萄球菌。使用包括23株催吐型蜡样芽孢杆菌和14株金黄色葡萄球菌在内的100株菌株评估了该检测方法的包容性和排他性。评估了从人工污染食品中分离DNA的不同方法,并使用已建立的实时检测方法分析了德国南部最近发生的两起催吐型食物中毒事件。其中一起食源性疾病暴发涉及17名在日托中心的儿童,他们在食用一份加热过的米饭菜肴后呕吐、虚脱并住院;另一起病例涉及食用花椰菜后发生的一起单一食物中毒事件。通过使用实时荧光定量PCR检测方法,在2小时内确定这些食物中毒事件的病原体为催吐型蜡样芽孢杆菌。