Evidence map›Paper›PMID 28558471›Full record

ArticleAnalytical chemistry2017

Dual Recognition Element Lateral Flow Assay Toward Multiplex Strain Specific Influenza Virus Detection.

Thao T Le, Pengxiang Chang, Donald J Benton, John W McCauley, Munir Iqbal, Anthony E G Cass

Abstract read
In one paragraph

Article in Analytical chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed.

  1. Review
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  5. Aptamer and DNAzyme Based Colorimetric Biosensors for Pathogen Detection.Angewandte Chemie (International ed. in English) · 2025
    Review
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  18. Aptamers for Viral Detection and Inhibition.ACS infectious diseases · 2022
    Review
  19. Aptamers-Diagnostic and Therapeutic Solution in SARS-CoV-2.International journal of molecular sciences · 2022
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Thao T LeDepartment of Chemistry, Imperial College London , London SW7 2AZ, U.K.
Pengxiang ChangAvian Viral Diseases Program, Pirbright Institute , Woking GU24 0NF, U.K.
Donald J BentonWorldwide Influenza Centre, Francis Crick Institute , London NW1 1AT, U.K.
John W McCauleyWorldwide Influenza Centre, Francis Crick Institute , London NW1 1AT, U.K.
Munir IqbalAvian Viral Diseases Program, Pirbright Institute , Woking GU24 0NF, U.K.
Anthony E G CassDepartment of Chemistry, Imperial College London , London SW7 2AZ, U.K.ORCID 0000-0001-8881-4786

Funding

Biotechnology and Biological Sciences Research Council BBS/E/I/00001708Biotechnology and Biological Sciences Research Council BBS/E/I/00007039Medical Research Council MC_U117585868Wellcome Trust
6 · The paper itself

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.

Indexed as

Antibodies, MonoclonalAptamers, NucleotideBiotinGoldHumansImmunoassayInfluenza A Virus, H3N2 SubtypeInfluenza, HumanMetal NanoparticlesPoint-of-Care SystemsSELEX Aptamer TechniqueStreptavidinAntibodies, MonoclonalAptamers, NucleotideBiotinGoldStreptavidin

Identifiers

PMID28558471
PMCPMC5514394

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.