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通过聚合酶链反应结合磁珠和毛细管电泳快速检测……(原文中“,,and ”部分内容缺失,无法准确完整翻译)

The Rapid Detection of , , and via Polymerase Chain Reaction Combined with Magnetic Beads and Capillary Electrophoresis.

作者信息

Ndraha Nodali, Lin Hung-Yun, Tsai Shou-Kuan, Hsiao Hsin-I, Lin Han-Jia

机构信息

Department of Bioscience and Biotechnology, National Taiwan Ocean University, Keelung 202301, Taiwan.

Center of Excellence for the Oceans, National Taiwan Ocean University, Keelung 202301, Taiwan.

出版信息

Foods. 2023 Oct 24;12(21):3895. doi: 10.3390/foods12213895.

Abstract

Food safety concerns regarding foodborne pathogen contamination have gained global attention due to its significant implications. In this study, we developed a detection system utilizing a PCR array combined with an automated magnetic bead-based system and CE technology to enable the detection of three foodborne pathogens, namely , , and . The results showed that our developed method could detect these pathogens at concentrations as low as 7.3 × 10, 6.7 × 10, and 6.9 × 10 cfu/mL, respectively, in the broth samples. In chicken samples, the limit of detection for these pathogens was 3.1 × 10, 3.5 × 10, and 3.9 × 10 cfu/g, respectively. The detection of these pathogens was accomplished without the necessity for sample enrichment, and the entire protocols, from sample preparation to amplicon analysis, were completed in approximately 3.5 h. Regarding the impact of the extraction method on detection capability, our study observed that an automated DNA extraction system based on the magnetic bead method demonstrated a 10-fold improvement or, at the very least, yielded similar results compared to the column-based method. These findings demonstrated that our developed model is effective in detecting low levels of these pathogens in the samples analyzed in this study. The PCR-CE method developed in this study may help monitor food safety in the future. It may also be extended to identify other foodborne pathogens across a wide range of food samples.

摘要

由于食源性病原体污染对食品安全的重大影响,其引发的食品安全问题已受到全球关注。在本研究中,我们开发了一种检测系统,该系统利用PCR阵列结合基于磁珠的自动化系统和CE技术,以实现对三种食源性病原体的检测,即 、 和 。结果表明,我们开发的方法能够在肉汤样品中分别检测到低至7.3×10、6.7×10和6.9×10 cfu/mL浓度的这些病原体。在鸡肉样品中,这些病原体的检测限分别为3.1×10、3.5×10和3.9×10 cfu/g。这些病原体的检测无需样品富集,并且从样品制备到扩增子分析的整个流程在大约3.5小时内即可完成。关于提取方法对检测能力的影响,我们的研究观察到,基于磁珠法的自动化DNA提取系统与基于柱法相比,检测能力提高了10倍,或者至少产生了相似的结果。这些发现表明,我们开发的模型在检测本研究中分析的样品中的低水平这些病原体方面是有效的。本研究中开发的PCR-CE方法可能有助于未来监测食品安全。它还可能被扩展用于识别广泛食品样品中的其他食源性病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7813/10649415/700f859fc78c/foods-12-03895-g001.jpg

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