Literature DB >> 29524216

Recombinase Polymerase Amplification Combined with Lateral Flow Strip for Listeria monocytogenes Detection in Food.

Xin-Jun Du1, Yu-Xuan Zang1, Hai-Bin Liu1, Ping Li1, Shuo Wang1,2.   

Abstract

Listeria monocytogenes is an important food-borne pathogenic bacterium that causes human disease, resulting in economic losses worldwide. The current detection methods for L. monocytogenes are not well suited for direct field testing because they involve complicated, time-consuming operations. A simple, efficient method is vital for L. monocytogenes detection. In this study, we combined isothermal recombinase polymerase amplification (RPA) with a lateral flow (LF) strip to rapidly and reliably detect L. monocytogenes. In the presence of biotin- and digoxin-modified primers, RPA produced numerous digoxin- and biotin-attached duplex DNA products. These products were detected on an LF strip via dual immunoreactions (digoxin on the duplex DNA reacted with the anti-digoxin antibody on the gold nanoparticle (Au-NP) and the biotin on the duplex DNA captured by the streptavidin on the LF test zone). The accumulation of Au-NPs produced characteristic bands, enabling the visual detection of L. monocytogenes without instrumentation. This assay could be used to detect L. monocytogenes within 15 min, including DNA amplification with RPA for 10 min at 39 °C and visualization of the amplicons by LF strips for 5 min. Experiments confirmed a detection limit as low as 300 fg of DNA and 1.5 × 101 CFU in pure cultures. Furthermore, RPA-LF exhibited no cross-reactions with pathogens. Evaluation of the method with food samples indicated that the detection limit was substantially improved to 1.5 × 10° CFU for the original bacterial content in 25 g/mL samples after enrichment for 6 hr. RPA-LF can be used as a sensitive and rapid detection technique for L. monocytogenes. PRACTICAL APPLICATION: Recombinase polymerase amplification (RPA) can amplify target DNA at 37 to 42 °C without a thermal cycler. Lateral flow (LF) strips are portable, cheap and easy to operate. RPA combined with LF strips to detect Listeria monocytogenes can be widely used in remote areas.
© 2018 Institute of Food Technologists®.

Entities:  

Keywords:  Listeria monocytogenes; lateral flow (LF) strip; rapid detection; recombinase polymerase amplification (RPA)

Mesh:

Substances:

Year:  2018        PMID: 29524216     DOI: 10.1111/1750-3841.14078

Source DB:  PubMed          Journal:  J Food Sci        ISSN: 0022-1147            Impact factor:   3.167


  8 in total

Review 1.  Antibody- and nucleic acid-based lateral flow immunoassay for Listeria monocytogenes detection.

Authors:  Matheus Bernardes Torres Fogaça; Arun K Bhunia; Leonardo Lopes-Luz; Eduardo Pimenta Ribeiro Pontes de Almeida; José Daniel Gonçalves Vieira; Samira Bührer-Sékula
Journal:  Anal Bioanal Chem       Date:  2021-05-26       Impact factor: 4.142

2.  A Rapid and Sensitive Europium Nanoparticle-Based Lateral Flow Immunoassay Combined with Recombinase Polymerase Amplification for Simultaneous Detection of Three Food-Borne Pathogens.

Authors:  Kai Chen; Biao Ma; Jiali Li; Erjing Chen; Ying Xu; Xiaoping Yu; Chuanxin Sun; Mingzhou Zhang
Journal:  Int J Environ Res Public Health       Date:  2021-04-26       Impact factor: 3.390

3.  Development of a lateral flow recombinase polymerase amplification assay for rapid and visual detection of Cryptococcus neoformans/C. gattii in cerebral spinal fluid.

Authors:  Qinglin Ma; Jilong Yao; Shixin Yuan; Houming Liu; Ning Wei; Jianming Zhang; Wanshui Shan
Journal:  BMC Infect Dis       Date:  2019-02-04       Impact factor: 3.090

4.  Multiplex Recombinase Polymerase Amplification Assay for the Simultaneous Detection of Three Foodborne Pathogens in Seafood.

Authors:  Biao Ma; Jiali Li; Kai Chen; Xiaoping Yu; Chuanxin Sun; Mingzhou Zhang
Journal:  Foods       Date:  2020-03-03

Review 5.  Recent advances in sensitivity enhancement for lateral flow assay.

Authors:  Yulin Deng; Hao Jiang; Xiaoqiong Li; Xuefei Lv
Journal:  Mikrochim Acta       Date:  2021-10-13       Impact factor: 5.833

Review 6.  A Review of Isothermal Amplification Methods and Food-Origin Inhibitors against Detecting Food-Borne Pathogens.

Authors:  Ye-Ji Moon; So-Young Lee; Se-Wook Oh
Journal:  Foods       Date:  2022-01-24

7.  Rapid detection of Enterococcus and vancomycin resistance using recombinase polymerase amplification.

Authors:  Pimchanok Panpru; Arpasiri Srisrattakarn; Nuttanun Panthasri; Patcharaporn Tippayawat; Aroonwadee Chanawong; Ratree Tavichakorntrakool; Jureerut Daduang; Lumyai Wonglakorn; Aroonlug Lulitanond
Journal:  PeerJ       Date:  2021-12-07       Impact factor: 2.984

8.  Applicability of duplex real time and lateral flow strip reverse-transcription recombinase aided amplification assays for the detection of Enterovirus 71 and Coxsackievirus A16.

Authors:  Xin-Na Li; Xin-Xin Shen; Ming-Hui Li; Ju-Ju Qi; Rui-Huan Wang; Qing-Xia Duan; Rui-Qing Zhang; Tao Fan; Xue-Ding Bai; Guo-Hao Fan; Yao Xie; Xue-Jun Ma
Journal:  Virol J       Date:  2019-12-30       Impact factor: 4.099

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.