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基于金纳米粒子的纸平台上 RNA 标志物的感应实现对活致病细菌的可视化和灵敏检测。

Visual and sensitive detection of viable pathogenic bacteria by sensing of RNA markers in gold nanoparticles based paper platform.

机构信息

MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.

MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.

出版信息

Biosens Bioelectron. 2014 Dec 15;62:38-46. doi: 10.1016/j.bios.2014.06.020. Epub 2014 Jun 14.

Abstract

Food-borne pathogens have been recognized as a major cause of human infections worldwide. Their identification needs to be simpler, cheaper and more reliable than the traditional methods. Here, we constructed a low-cost paper platform for viable pathogenic bacteria detection with the naked eye. In this study, an effective isothermal amplification method was used to amplify the hlyA mRNA gene, a specific RNA marker in Listeria monocytogenes. The amplification products were applied to the paper-based platform to perform a visual test using sandwich hybridization assays. When the RNA products migrated along the platform by capillary action, the gold nanoparticles accumulated at the designated area. Under optimized experimental conditions, as little as 0.5 pg/μL genomic RNA from L. monocytogenes could be detected. It could also be used to specifically detect 20 CFU/mL L. monocytogenes from actual samples. The whole assay process, including RNA extraction, amplification, and visualization, can be completed within several hours. This method is suitable for point-of-care applications to detect food-borne pathogens, as it can overcome the false-positive results caused by amplifying nonviable L. monocytogenes. Furthermore, the results can be imaged and transformed into a two-dimensional bar code through an Android-based smart phone for further analysis or in-field food safety tracking.

摘要

食源性致病菌已被认为是全世界人类感染的主要原因。与传统方法相比,它们的鉴定需要更简单、更便宜、更可靠。在这里,我们构建了一个用于肉眼检测活菌的低成本纸质平台。在这项研究中,使用一种有效的等温扩增方法来扩增李斯特菌 hlyA mRNA 基因,这是李斯特菌的一种特异性 RNA 标记。将扩增产物应用于基于纸张的平台,通过夹心杂交测定进行目视检测。当 RNA 产物通过毛细作用沿平台迁移时,金纳米粒子在指定区域聚集。在优化的实验条件下,可检测到低至 0.5 pg/μL 的单核细胞增生李斯特菌基因组 RNA。它还可以专门检测实际样本中 20 CFU/mL 的单核细胞增生李斯特菌。整个检测过程,包括 RNA 提取、扩增和可视化,可在数小时内完成。该方法适用于即时检测应用,可用于检测食源性致病菌,因为它可以克服扩增非存活李斯特菌引起的假阳性结果。此外,还可以通过基于 Android 的智能手机对结果进行成像,并将其转换为二维条码,以便进一步分析或现场食品安全跟踪。

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