Detection of metazoan species as a public health issue: simple methods for the validation of food safety and quality.

O Vassioukovitch, M Orsini, A Paparini, G Gianfranceschi, O Cattarini, P Di Michele, E Montuori, G C Vanini, V Romano Spica
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引用次数: 4

Abstract

Species identification represents a critical issue in food chain safety and quality control. Several procedures are available to detect animal proteins in cattle feed or to trace transgenic foods. The most effective approach is based on the use of DNA as a marker. Amplification of DNA provides rapid, sensitive and specific protocols. Several target genes can be used, but new insights come from the mitochondrial genome, which is naturally amplified in each cell and shows a remarkable resistance to degradation. These are key points when analysing complex matrices such as foods, animal feedstuff or environmental samples. Traceability is important to prevent BSE or to monitor novel foods, such as genetically modified organisms. Amplification is commonly performed, but it requires expertise and a molecular biology laboratory to perform restriction analysis, electrophoresis or gel staining for the visualisation of results. Hereby, we consider a strategy based on multiple nested amplification and reverse hybridisation assay that virtually requires only a thermocycler and a water bath. The protocol is rapid and simple and can simultaneously detect different species in a DNA sample. This promising approach allows microarray developments, opening up to further perspectives. An international application has been published under the patent cooperation treaty. Presently, a ban on feeding ruminants on cattle-derived proteins is in force in Europe and USA. The identification of metazoan traces in a sample is not only a mere preventive measure for BSE, but represents a possible screening system for monitoring biotechnology products and procedures, as well as a quality control strategy to assure consumer's rights.

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作为公共卫生问题的后生动物的检测:验证食品安全和质量的简单方法。
物种鉴定是食品链安全和质量控制中的一个关键问题。有几种方法可用于检测牛饲料中的动物蛋白或追踪转基因食品。最有效的方法是利用DNA作为标记。DNA扩增提供快速,敏感和特定的协议。可以使用几个目标基因,但线粒体基因组带来了新的见解,线粒体基因组在每个细胞中自然扩增,并表现出非凡的抗降解能力。这些是分析复杂基质(如食品、动物饲料或环境样品)时的关键点。可追溯性对于预防疯牛病或监测新型食品(如转基因生物)非常重要。通常进行扩增,但它需要专业知识和分子生物学实验室进行限制性酶切分析,电泳或凝胶染色以实现结果的可视化。因此,我们考虑了一种基于多重嵌套扩增和反向杂交分析的策略,实际上只需要一个热循环器和一个水浴。该方法快速简便,可以同时检测DNA样本中的不同物种。这种有前途的方法允许微阵列的发展,开辟了进一步的观点。根据专利合作条约公布了一项国际申请。目前,欧洲和美国正在实施一项禁止用牛源性蛋白质喂养反刍动物的禁令。在样本中识别后生动物的痕迹不仅是对疯牛病的一种预防措施,而且代表了一种可能的监测生物技术产品和程序的筛选系统,以及确保消费者权利的质量控制策略。
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