Evidence map›Paper›PMID 27460437›Full record

ArticleScientific reports2016

Rapid identification of intact bacterial resistance plasmids via optical mapping of single DNA molecules.

Lena K Nyberg, Saair Quaderi, Gustav Emilsson, Nahid Karami, Erik Lagerstedt, Vilhelm Müller, Charleston Noble, Susanna Hammarberg, Adam N Nilsson, Fei Sjöberg and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Strain-Level Typing ofACS infectious diseases · 2025
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  8. Identity ofMicroorganisms · 2021
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  15. Phosphorylated CtIP bridges DNA to promote annealing of broken ends.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Lena K NybergDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Saair QuaderiDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Gustav EmilssonDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Nahid KaramiDepartment of Infectious Diseases, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Erik LagerstedtDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Vilhelm MüllerDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Charleston NobleDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Susanna HammarbergDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Adam N NilssonDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Fei SjöbergDepartment of Infectious Diseases, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Joachim FritzscheDepartment of Applied Physics, Chalmers University of Technology, Gothenburg, Sweden.
Erik KristianssonDepartment of Mathematical Sciences, Chalmers University of Technology/University of Gothenburg, Gothenburg, Sweden.
Linus SandegrenDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Tobias AmbjörnssonDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Fredrik WesterlundDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapid spread of antibiotic resistance - currently one of the greatest threats to human health according to WHO - is to a large extent enabled by plasmid-mediated horizontal transfer of resistance genes. Rapid identification and characterization of plasmids is thus important both for individual clinical outcomes and for epidemiological monitoring of antibiotic resistance. Toward this aim, we have developed an optical DNA mapping procedure where individual intact plasmids are elongated within nanofluidic channels and visualized through fluorescence microscopy, yielding barcodes that reflect the underlying sequence. The assay rapidly identifies plasmids through statistical comparisons with barcodes based on publicly available sequence repositories and also enables detection of structural variations. Since the assay yields holistic sequence information for individual intact plasmids, it is an ideal complement to next generation sequencing efforts which involve reassembly of sequence reads from fragmented DNA molecules. The assay should be applicable in microbiology labs around the world in applications ranging from fundamental plasmid biology to clinical epidemiology and diagnostics.

Indexed as

BacteriaDNADNA Barcoding, TaxonomicDrug Resistance, BacterialFluorescent DyesMicrofluidicsOptical ImagingPlasmidsDNAFluorescent Dyes

Identifiers

PMID27460437
PMCPMC4961956

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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.