Evidence map›Paper›PMID 26068926›Full record

ArticlePloS one2015

Optical Imaging of Paramagnetic Bead-DNA Aggregation Inhibition Allows for Low Copy Number Detection of Infectious Pathogens.

Jacquelyn A DuVall, Juliane C Borba, Nazly Shafagati, Deborah Luzader, Nishant Shukla, Jingyi Li, Kylene Kehn-Hall, Melissa M Kendall, Sanford H Feldman, James P Landers

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
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

7 citing papers in PubMed, 25 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Jacquelyn A DuVallDepartment of Chemistry, University of Virginia, Charlottesville, VA, United States of America.
Juliane C BorbaDepartment of Chemistry, University of Virginia, Charlottesville, VA, United States of America.
Nazly ShafagatiNational Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA, United States of America.
Deborah LuzaderDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA, United States of America.
Nishant ShuklaDepartment of Computer Science, University of Virginia, Charlottesville, VA, United States of America.
Jingyi LiDepartment of Chemistry, University of Virginia, Charlottesville, VA, United States of America.
Kylene Kehn-HallNational Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA, United States of America.
Melissa M KendallDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA, United States of America.
Sanford H FeldmanCenter for Comparative Medicine, University of Virginia, Charlottesville, VA, United States of America.
James P LandersDepartment of Chemistry, University of Virginia, Charlottesville, VA, United States of America; Department of Mechanical Engineering, University of Virginia, Charlottesville, VA, United States of America; Department of Pathology, University of Virginia, Charlottesville, VA, United States of America.
University of Virginia · USGeorge Mason University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA-paramagnetic silica bead aggregation in a rotating magnetic field facilitates the quantification of DNA with femtogram sensitivity, but yields no sequence-specific information. Here we provide an original description of aggregation inhibition for the detection of DNA and RNA in a sequence-specific manner following loop-mediated isothermal amplification (LAMP). The fragments generated via LAMP fail to induce chaotrope-mediated bead aggregation; however, due to their ability to passivate the bead surface, they effectively inhibit bead aggregation by longer 'trigger' DNA. We demonstrate the utility of aggregation inhibition as a method for the detection of bacterial and viral pathogens with sensitivity that approaches single copies of the target. We successfully use this methodology for the detection of notable food-borne pathogens Escherichia coli O157:H7 and Salmonella enterica, as well as Rift Valley fever virus, a weaponizable virus of national security concern. We also show the concentration dependence of aggregation inhibition, suggesting the potential for quantification of target nucleic acid in clinical and environmental samples. Lastly, we demonstrate the ability to rapidly detect infectious pathogens by utilizing a cell phone and custom-written application (App), making this novel detection modality fully portable for point-of-care use.

Indexed as

AnimalsCell PhoneDNADNA PrimersEscherichia coli InfectionsEscherichia coli O157HumansMagneticsNucleic Acid Amplification TechniquesOptical ImagingPoint-of-Care SystemsPolymerase Chain ReactionRift Valley FeverRift Valley fever virusSalmonella entericaSilicon DioxideDNADNA PrimersSilicon Dioxide

Identifiers

PMID26068926
PMCPMC4466016
OpenAlexW1898548929

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.