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分析生物缀合物、适体能够特异性定量检测单核细胞增生李斯特菌。

Analytical bioconjugates, aptamers, enable specific quantitative detection of Listeria monocytogenes.

机构信息

Department of Microbiology, Chungbuk National University, 1 Chungdae-Ro, Seowon-Gu, Cheongju 362-763, South Korea.

Division of Endocrinology & Metabolism, Department of Internal Medicine, Chonbuk National University Medical School, 634-18 Geumam-Dong, Duckjin-Gu, Jeonju 561-712, South Korea.

出版信息

Biosens Bioelectron. 2015 Jun 15;68:272-280. doi: 10.1016/j.bios.2015.01.009. Epub 2015 Jan 3.

Abstract

As a major human pathogen in the Listeria genus, Listeria monocytogenes causes the bacterial disease listeriosis, which is a serious infection caused by eating food contaminated with the bacteria. We have developed an aptamer-based sandwich assay (ABSA) platform that demonstrates a promising potential for use in pathogen detection using aptamers as analytical bioconjugates. The whole-bacteria SELEX (WB-SELEX) strategy was adopted to generate aptamers with high affinity and specificity against live L. monocytogenes. Of the 35 aptamer candidates tested, LMCA2 and LMCA26 reacted to L. monocytogenes with high binding, and were consequently chosen as sensing probes. The ABSA platform can significantly enhance the sensitivity by employing a very specific aptamer pair for the sandwich complex. The ABSA platform exhibited a linear response over a wide concentration range of L. monocytogenes from 20 to 2×10(6) CFU per mL and was closely correlated with the following relationship: y=9533.3x+1542.3 (R(2)=0.99). Our proposed ABSA platform also provided excellent specificity for the tests to distinguish L. monocytogenes from other Listeria species and other bacterial genera (3 Listeria spp., 4 Salmonella spp., 2 Vibrio spp., 3 Escherichia coli and 3 Shigella spp.). Improvements in the sensitivity and specificity have not only facilitated the reliable detection of L. monocytogenes at extremely low concentrations, but also allowed for the development of a 96-well plate-based routine assay platform for multivalent diagnostics.

摘要

作为李斯特菌属中的主要人类病原体,单核细胞增生李斯特菌会引起李斯特菌病,这是一种因食用受细菌污染的食物而导致的严重感染。我们开发了一种基于适配体的三明治检测(ABSA)平台,该平台使用适配体作为分析生物缀合物,具有用于病原体检测的巨大潜力。采用全菌 SELEX(WB-SELEX)策略来生成对活李斯特菌具有高亲和力和特异性的适配体。在测试的 35 个适配体候选物中,LMCA2 和 LMCA26 与单核细胞增生李斯特菌的结合反应强烈,因此被选为传感探针。ABSA 平台通过使用非常特异的适配体对夹心复合物进行检测,可以显著提高检测的灵敏度。ABSA 平台在 20 至 2×10(6) CFU/mL 的广泛李斯特菌浓度范围内呈现出线性响应,并且与以下关系密切相关:y=9533.3x+1542.3(R(2)=0.99)。我们提出的 ABSA 平台还为测试提供了出色的特异性,以区分李斯特菌与其他李斯特菌属和其他细菌属(3 种李斯特菌属、4 种沙门氏菌属、2 种弧菌属、3 种大肠杆菌和 3 种志贺氏菌属)。灵敏度和特异性的提高不仅促进了对极低浓度李斯特菌的可靠检测,而且还开发了一种基于 96 孔板的多价诊断常规检测平台。

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