Evidence map›Paper›PMID 35660772›Full record

ArticleScientific reports2022

A simple cut and stretch assay to detect antimicrobial resistance genes on bacterial plasmids by single-molecule fluorescence microscopy.

Gaurav Goyal, Elina Ekedahl, My Nyblom, Jens Krog, Erik Fröbrant, Magnus Brander, Tsegaye Sewunet, Teerawit Tangkoskul, Christian G Giske, Linus Sandegren and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 11 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

13 authors at 6 institutions in 2 countries.

Gaurav Goyal *Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Elina Ekedahl *Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
My NyblomDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Jens KrogDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Erik FröbrantDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Magnus BranderDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Tsegaye SewunetDepartment of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.
Teerawit TangkoskulFaculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Christian G GiskeDepartment of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.
Linus SandegrenDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Visanu ThamlikitkulFaculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Tobias AmbjörnssonDepartment of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
Fredrik WesterlundDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden. fredrikw@chalmers.se.ORCID 0000-0002-4767-4868
Chalmers University of Technology · SELund University · SESiriraj Hospital · THKarolinska Institutet · SEKarolinska University Hospital · SEUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial resistance (AMR) is a fast-growing threat to global health. The genes conferring AMR to bacteria are often located on plasmids, circular extrachromosomal DNA molecules that can be transferred between bacterial strains and species. Therefore, effective methods to characterize bacterial plasmids and detect the presence of resistance genes can assist in managing AMR, for example, during outbreaks in hospitals. However, existing methods for plasmid analysis either provide limited information or are expensive and challenging to implement in low-resource settings. Herein, we present a simple assay based on CRISPR/Cas9 excision and DNA combing to detect antimicrobial resistance genes on bacterial plasmids. Cas9 recognizes the gene of interest and makes a double-stranded DNA cut, causing the circular plasmid to linearize. The change in plasmid configuration from circular to linear, and hence the presence of the AMR gene, is detected by stretching the plasmids on a glass surface and visualizing by fluorescence microscopy. This single-molecule imaging based assay is inexpensive, fast, and in addition to detecting the presence of AMR genes, it provides detailed information on the number and size of plasmids in the sample. We demonstrate the detection of several β-lactamase-encoding genes on plasmids isolated from clinical samples. Furthermore, we demonstrate that the assay can be performed using standard microbiology and clinical laboratory equipment, making it suitable for low-resource settings.

Indexed as

Anti-Bacterial AgentsSingle Molecule ImagingBacteriaDrug Resistance, BacterialMicroscopy, FluorescencePlasmidsAnti-Bacterial Agents

Identifiers

PMID35660772
PMCPMC9166776
OpenAlexW4281668842

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LicenceCC BY
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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.