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Evaluation of the Optimal Multiplex PCR Method for the Detection of Aspergillus Flavus and Aspergillus Parasiticus on Dried Peanut

机译:评价对干燥花生曲霉和曲霉伞菌检测的最佳多重PCR方法

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Aspergillus flavus and Aspergillus parasiticus are the common aflatoxin producing species that usually infect on foodstuff in their production line from the field to the storage place such as peanut, corn, cereal, etc., especially in tropical country like Vietnam. Aflatoxins which are considered as derived secondary metabolites assigned as a group of mycotoxins produced by several species of the Aspergillus spp are potent hepatotoxins, immunosuppression, carcinogen that lead to mortality or reducing the productivity of farm animals. There has been a demand for effective method to detect these two species on dried food. In previous study, a multiplex PCR method were designed to improve the detection process of A. flavus and A. parasiticus and that method showed high sensitivity and specificity by being applied on artificially infected dried peanut. In this study, that multiplex PCR method would be evaluated by testing the presence of A. flavus and A. parasiticus on natural dried peanut kernels. On this purpose, the presence of A. flavus and A. parasiticus on the collected peanut from the market was determined using two method, the conventional culturing method in Institute of Hygiene and Public Health (THPH) and the mentioned multiplex PCR. The efficiency of multiplex PCR method would be evaluated by comparing fungi detection result of two methods using appropriate statistical tests. Next, fungal enrichment with distilled water overnight was applied to increase the detection percentage if the first analysis do not get the expected result The result showed that 54% results from PCR method was the same with culturing method, and after fungal enrichment, this percentage increased to 76% which suggested that these two method was not significantly different with each other. Therefore, this multiplex PCR method could have more advanced points than the culturing method in detection of A. flavus and A. parasiticus on foodstuff.
机译:曲霉菌和曲霉菌碱是常见的黄曲霉毒素生产物种,通常在其生产线上的食品中从现场感染到储舍,玉米,谷物等,特别是在像越南这样的热带国家。被认为是衍生的二次代谢物作为一组由几种曲霉属SPP产生的一组霉菌毒素,是有效的肝毒素,免疫抑制,致癌物质,导致死亡率或降低农场动物的生产率。需要有效的方法来检测干燥食物上这两个物种。在先前的研究中,设计了一种多重PCR方法以改善A.FlaVus和A.寄生菌的检测过程,并且通过在人工感染的干燥花生上应用,该方法表现出高敏感性和特异性。在本研究中,通过测试天然干燥花生核上的A.FlaVus和A.寄生虫的存在来评估多重PCR方法。这样的目的,使用两个方法中,在卫生和公共健康(THPH)研究所的常规培养方法和所提到的多重PCR测定黄曲霉和寄生曲霉的从市场所收集的花生的存在。通过使用适当的统计测试比较两种方法的真菌检测结果来评估多重PCR方法的效率。接下来,施用蒸馏水的真菌富集用于增加检测百分比,如果第一次分析没有得到预期的结果,结果表明,PCR方法的54%结果与培养方法相同,并且在真菌富集后,这种百分比增加了76%表明这两种方法彼此没有显着不同。因此,这种多重PCR方法可以具有比在食品上检测A.Flavus和A.寄生虫的培养方法更高的点。

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