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

被引:70
作者
Lee, Sang-Hee [1 ]
Ahn, Ji-Young [1 ]
Lee, Kyeong-Ah [1 ]
Um, Hyun-Ju [1 ]
Sekhon, Simranjeet Singh [1 ]
Park, Tae Sun [2 ]
Min, Jiho [3 ]
Kim, Yang-Hoon [1 ]
机构
[1] Chungbuk Natl Univ, Dept Microbiol, Cheongju 362763, South Korea
[2] Chonbuk Natl Univ, Sch Med, Dept Internal Med, Div Endocrinol & Metab, Jeonju 561712, South Korea
[3] Chonbuk Natl Univ, Grad Sch Semicond & Chem Engn, Jeonju 561756, South Korea
基金
新加坡国家研究基金会;
关键词
Listeria monocytogenes; Aptamer-based Sandwich Assay (ABSA); platform; Whole-bacteria SELEX (WB-SELEX); Analytical bioconjugates; Aptamer; SURFACE-PLASMON RESONANCE; REAL-TIME PCR; IMMUNOMAGNETIC SEPARATION; SIGNAL AMPLIFICATION; SALMONELLA-ENTERICA; SENSITIVE DETECTION; MODIFIED ELECTRODES; COLI O157/H7; BIOSENSOR; QUANTIFICATION;
D O I
10.1016/j.bios.2015.01.009
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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 Listeria monocytogenes. Of the 35 aptamer candidates tested, LMCA2 and LMCA26 reacted to Listeria 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 Listeria monocytogenes from 20 to 2 x 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 Listeria 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 Listeria monocytogenes at extremely low concentrations, but also allowed for the development of a 96-well plate-based routine assay platform for multivalent diagnostics. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:272 / 280
页数:9
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