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Dual recognition element lateral flow assay (DRELFA) towards multiplex strain-specific influenza virus detection
File | Description | Size | Format | |
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Supporting Information.pdf | Supporting information | 353.94 kB | Adobe PDF | View/Open |
acs.analchem.7b01149.pdf | Published version | 3.04 MB | Adobe PDF | View/Open |
Title: | Dual recognition element lateral flow assay (DRELFA) towards multiplex strain-specific influenza virus detection |
Authors: | Le, T Chang, P Benton, DJ McCauley, JW Iqbal, M Cass, AEG |
Item Type: | Journal Article |
Abstract: | Different influenza virus strains have caused a number of recent outbreaks killing scores of people and causing significant losses in animal farming. Simple, rapid, sensitive, and specific detection of particular strains, such as a pandemic strain versus a previous seasonal influenza, plays a crucial role in the monitoring, controlling, and management of outbreaks. In this paper we describe a dual recognition element lateral flow assay (DRELFA) which pairs a nucleic acid aptamer with an antibody for use as a point-of-care platform which can detect particular strains of interest. The combination is used to overcome the individual limitations of antibodies’ cross-reactivity and aptamers’ slow binding kinetics. In the detection of influenza viruses, we show that DRELFA can discriminate a particular virus strain against others of the same subtype or common respiratory diseases while still exhibiting fast binding kinetic of the antibody-based lateral flow assay (LFA). The improvement in specificity that DRELFA exhibits is an advantage over the currently available antibody-based LFA systems for influenza viruses, which offer discrimination between influenza virus types and subtypes. Using quantitative real-time PCR (qRT-PCR), it showed that the DRELFA is very effective in localizing the analyte to the test line (consistently over 90%) and this is crucial for the sensitivity of the device. In addition, color intensities of the test lines showed a good correlation between the DRELFA and the qRT-PCR over a 50-fold concentration range. Finally, lateral flow strips with a streptavidin capture test line and an anti-antibody control line are universally applicable to specific detection of a wide range of different analytes. |
Issue Date: | 30-May-2017 |
Date of Acceptance: | 30-May-2017 |
URI: | http://hdl.handle.net/10044/1/48848 |
DOI: | https://dx.doi.org/10.1021/acs.analchem.7b01149 |
ISSN: | 1520-6882 |
Publisher: | American Chemical Society |
Start Page: | 6781 |
End Page: | 6786 |
Journal / Book Title: | Analytical Chemistry |
Volume: | 89 |
Issue: | 12 |
Copyright Statement: | © 2017 American Chemical Society. ACS AuthorChoice - This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
Sponsor/Funder: | Biotechnology and Biological Sciences Research Cou |
Funder's Grant Number: | PON 4090041903 |
Keywords: | Science & Technology Physical Sciences Chemistry, Analytical Chemistry A VIRUS PANDEMIC H1N1 VIRAL LOADS APTAMER HEMAGGLUTININ RNA ANTIBODIES IMMUNOASSAY BIND H5N1 Analytical Chemistry 0301 Analytical Chemistry 0904 Chemical Engineering 0399 Other Chemical Sciences |
Publication Status: | Published |
Appears in Collections: | Chemistry Biological and Biophysical Chemistry Faculty of Natural Sciences |