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Food Microbial Pathogen Detection and Analysis Using DNA Microarray Technologies

机译:使用DNA芯片技术对食品微生物病原体进行检测和分析

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摘要

Culture-based methods used for microbial detection and identification are simple to use, relatively inexpensive, and sensitive. However, culture-based methods are too time-consuming for high-throughput testing and too tedious for analysis of samples with multiple organisms and provide little clinical information regarding the pathogen (e.g., antibiotic resistance genes, virulence factors, or strain subtype). DNA-based methods, such as polymerase chain reaction (PCR), overcome some these limitations since they are generally faster and can provide more information than culture-based methods. One limitation of traditional PCR-based methods is that they are normally limited to the analysis of a single pathogen, a small group of related pathogens, or a small number of relevant genes. Microarray technology enables a significant expansion of the capability of DNA-based methods in terms of the number of DNA sequences that can be analyzed simultaneously, enabling molecular identification and characterization of multiple pathogens and many genes in a single array assay. Microarray analysis of microbial pathogens has potential uses in research, food safety, medical, agricultural, regulatory, public health, and industrial settings. In this article, we describe the main technical elements of microarray technology and the application and potential use of DNA microarrays for food microbial analysis.
机译:用于微生物检测和鉴定的基于培养物的方法使用简单,相对便宜且敏感。然而,基于培养物的方法对于高通量测试而言既费时,又对于分析具有多种生物的样品而言过于繁琐,并且很少提供有关病原体的临床信息(例如,抗生素抗性基因,毒力因子或菌株亚型)。基于DNA的方法(例如聚合酶链反应(PCR))克服了这些局限性,因为它们通常比基于培养的方法更快,并且可以提供更多信息。传统的基于PCR的方法的局限性在于,它们通常仅限于分析单个病原体,一小组相关病原体或少量相关基因。微阵列技术极大地扩展了可同时分析的DNA序列数量方面基于DNA的方法的能力,从而可以在单个阵列测定中对多种病原体和许多基因进行分子鉴定和表征。微生物病原体的微阵列分析在研究,食品安全,医疗,农业,法规,公共卫生和工业环境中具有潜在用途。在本文中,我们描述了微阵列技术的主要技术要素以及DNA微阵列在食品微生物分析中的应用和潜在用途。

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