{"title":"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","authors":"B. Çöl, H. Aksu","doi":"10.30704/http-www-jivs-net.1198813","DOIUrl":null,"url":null,"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.","PeriodicalId":142259,"journal":{"name":"Journal of Istanbul Veterinary Sciences","volume":"281 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"A study on toxin genes and cytotoxity levels of Bacillus cereus in various ready to eat foods and pastry products in Turkey\",\"authors\":\"B. Çöl, H. Aksu\",\"doi\":\"10.30704/http-www-jivs-net.1198813\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":142259,\"journal\":{\"name\":\"Journal of Istanbul Veterinary Sciences\",\"volume\":\"281 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Istanbul Veterinary Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.30704/http-www-jivs-net.1198813\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Istanbul Veterinary Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30704/http-www-jivs-net.1198813","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A study on toxin genes and cytotoxity levels of Bacillus cereus in various ready to eat foods and pastry products in Turkey
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.