A study on toxin genes and cytotoxity levels of Bacillus cereus in various ready to eat foods and pastry products in Turkey

B. Çöl, H. Aksu
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引用次数: 1

Abstract

Bacillus cereus is a spore-forming and toxin-producing gram-positive bacteria widely isolated from soils, meat, milk, and vegetables. It is recognized as one of the pathogenic bacteria that can lead to food poisoning and food spoilage in food service systems due to its ease of contamination of foods and lack of guarantee of elimination by pasteurization and sanitation practices. B. cereus causes two types of diseases mainly characterized by diarrhea and vomiting type syndrome with the toxins it produces. Toxins produced by B. cereus are mainly heat-stable emetic toxins and three different heat-labile enterotoxins. Foodborne illnesses of the diarrheal type are caused by the single proteins cytotoxin K (CytK), hemolysin BL (Hbl), and non-hemolytic enterotoxin (Nhe), whereas those of the emetic type, are caused by an emetic toxin. In this study, 225 ready-to-eat foods and pastry products were analyzed for B. cereus, its toxin profiles and cytotoxicity effect. Multiplex PCR is used to identify the presence of the Hbl, Nhe, CytK, and emetic toxin encoding genes. Component-specific antibody-based ELISA tests were utilized to determine the Hbl-L2 and NheB components. Cytotoxic activity of the B. cereus isolates on Vero cells was also identified. In total, B. cereus was detected in 36 out of 225 (16%) food samples. From the positive 36 B. cereus isolates, the ces gene was not identified, whereas 94.4% (34) Nhe, 58.3% (21) Hbl, and 5.5% (2) CytK encoding genes revealed positive results on PCR analysis. PCR results were also compatible with ELISA and Cytotoxicity tests. In a nutshell, 16% prevalence of B. cereus in foods is insufficient, and the presence or absence of toxin genes may not yield reliable results. It is critical to detect pathogenic B. cereus toxin gene profiles as well as toxin production ability at the same time. This study presents for the first time, data from a cell culture cytotoxicity test using specific monoclonal antibody-based sandwich ELISA and multiplex PCR for ready-to-eat foods and pastry products in Turkey.
土耳其各种即食食品和糕点制品中蜡样芽孢杆菌毒素基因和细胞毒性水平的研究
蜡样芽孢杆菌是一种产芽孢和毒素的革兰氏阳性细菌,广泛分离于土壤、肉类、牛奶和蔬菜中。它被认为是食品服务系统中可导致食物中毒和食物腐败的致病菌之一,因为它易于污染食品,并且缺乏通过巴氏消毒和卫生措施消除的保证。蜡样芽孢杆菌以其产生的毒素引起以腹泻和呕吐型综合征为主要特征的两类疾病。蜡样芽孢杆菌产生的毒素主要是热稳定型催吐毒素和三种不同的热不稳定型肠毒素。腹泻型食源性疾病是由单一蛋白细胞毒素K (CytK)、溶血素BL (Hbl)和非溶血性肠毒素(Nhe)引起的,而催吐型疾病是由催吐毒素引起的。本研究分析了225种即食食品和糕点产品的蜡样芽孢杆菌及其毒素谱和细胞毒性作用。多重PCR用于鉴定Hbl、Nhe、CytK和催吐毒素编码基因的存在。采用基于组分特异性抗体的ELISA检测hb - l2和NheB组分。蜡样芽孢杆菌分离株对Vero细胞的细胞毒活性也得到了鉴定。225份食物样本中有36份(16%)检出蜡样芽孢杆菌。36株蜡样芽孢杆菌阳性分离株中,未检出ces基因,而94.4%(34)的Nhe、58.3%(21)的Hbl和5.5%(2)的CytK编码基因的PCR检测结果为阳性。PCR结果与酶联免疫吸附试验和细胞毒性试验结果一致。简而言之,16%的蜡样芽孢杆菌在食物中的流行率是不够的,毒素基因的存在或不存在可能无法产生可靠的结果。在检测蜡样芽孢杆菌致病性毒素基因谱的同时,检测其产毒能力至关重要。本研究首次提出了使用基于特异性单克隆抗体的夹心ELISA和多重PCR对土耳其即食食品和糕点产品进行细胞培养细胞毒性测试的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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