Evidence map›Paper›PMID 31370820›Full record

ArticleBMC biotechnology2019

Lack of specificity associated with using molecular beacons in loop mediated amplification assays.

Patrick Hardinge, James A H Murray

Abstract read
In one paragraph

Article in BMC biotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Infection and drug resistance · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Loop-Mediated Isothermal Amplification: From Theory to Practice.Russian journal of bioorganic chemistry · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Quantitative LAMP and PCR Detection ofInternational journal of food science · 2020
    Article
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

2 authors.

Patrick HardingeCardiff School of Biosciences, Cardiff, Museum Avenue, Cardiff, CF10 3AX, UK. hardingep@cardiff.ac.uk.ORCID 0000-0002-6292-5186
James A H MurrayCardiff School of Biosciences, Cardiff, Museum Avenue, Cardiff, CF10 3AX, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/G017336/1Biotechnology and Biological Sciences Research Council BB/L022346/1
6 · The paper itself

Abstract

backgroundLoop mediated isothermal amplification of nucleic acid templates is a rapid, sensitive and specific method suitable for molecular diagnostics. However the complexity of primer design and the number of primers involved can lead to false positives from non-specific primer interactions. Standard methods of LAMP detection utilise the increasing concentrations of DNA or inorganic pyrophosphate and therefore lack specificity for identifying the desired LAMP amplification. Molecular beacons used in PCR reactions are target specific and may enhance specificity with LAMP.

resultsWe present a potential molecular beacon approach to LAMP detection targeting the single stranded region between loops, and test this for LAMP molecular beacons targeting the 35S promoter and NOS terminator sequences commonly used in GM crops. From these studies we show that molecular beacons used in LAMP, despite providing a change in fluorescent intensity with amplification, appear not to anneal to specific target sequences and therefore target specificity is not a benefit of this method. However, molecular beacons demonstrate a change in fluorescence which is indicative of LAMP amplification products. We identify the LAMP loop structure as likely to be responsible for this change in signal.

conclusionsMolecular beacons can be used to detect LAMP amplification but do not provide sequence specificity. The method can be used to determine effectively LAMP amplification from other primer-driven events, but does not discriminate between different LAMP amplicons. It is therefore unsuitable for multiplex LAMP reactions due to non-specific detection of LAMP amplification.

Indexed as

Base SequenceCrops, AgriculturalDNA, PlantDNA PrimersNucleic Acid Amplification TechniquesPlants, Genetically ModifiedPolymerase Chain ReactionPromoter Regions, GeneticReproducibility of ResultsSequence Homology, Nucleic AcidDNA, PlantDNA PrimersDNAFluorescenceGenetically modified (GM) cropsLoop-mediated amplification (LAMP)Molecular beacons

Identifiers

PMID31370820
PMCPMC6676609

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Registered trials

None linked

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.