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首页> 外文期刊>Applied and Environmental Microbiology >Diagnostic Real-Time PCR Assays for the Detection of Emetic Bacillus cereus Strains in Foods and Recent Food-Borne Outbreaks
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Diagnostic Real-Time PCR Assays for the Detection of Emetic Bacillus cereus Strains in Foods and Recent Food-Borne Outbreaks

机译:诊断实时荧光定量PCR检测食品中的催吐芽孢杆菌菌株和最近的食源性暴发

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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.
机译:产生蜡状内酯的蜡状芽孢杆菌可引起一种催吐型食源性疾病,其模仿金黄色葡萄球菌引起的症状。基于最近发现的蜡样芽孢杆菌形成的遗传背景,开发了一种新型的5'核酸酶(TaqMan)实时PCR测定法,以提供一种快速灵敏的方法来特异性检测食品中的蜡样芽孢杆菌。 TaqMan分析包括一个内部扩增对照,引物和一个设计为针对蜡样内酯合成酶基因的高度特异性部分的探针。此外,开发了一种特殊的SYBR green I测定法,并将其扩展为创建一种双步SYBR green I测定法,用于一步鉴定和区分引起呕吐的两种食物病原体B. cereus和金黄色葡萄球菌。使用一组包含100株催产芽孢杆菌和14株金黄色葡萄球菌的100株菌株对试验的包容性和排他性进行了评估。评估了从人造污染食品中分离DNA的不同方法,并建立了实时分析方法,用于分析德国南部最近发生的两次呕吐食品中毒事件。一次食源性疾病暴发包括前往日托中心的17名儿童,他们在食用了重新加热的米饭后呕吐,倒塌并入院;另一起案件涉及食用菜花后发生的一次食物中毒事件。在2小时内,通过实时PCR检测将这些食物中毒的病原体鉴定为催吐型蜡状芽孢杆菌。

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