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Updated: Sep 21, 2025

Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach
Published on: December 14, 2019
A simple cut and stretch assay to detect antimicrobial resistance genes on bacterial plasmids by single-molecule
Gaurav Goyal1, Elina Ekedahl1, My Nyblom1
1Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
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.
Insights
A new CRISPR-Cas9 assay simplifies detecting antimicrobial resistance (AMR) genes on bacterial plasmids. This method is fast, inexpensive, and suitable for low-resource settings, aiding in managing AMR threats.
Area of Science:
- Molecular Biology
- Genetics
- Microbiology
Background:
- Antimicrobial resistance (AMR) poses a significant global health challenge.
- AMR genes are frequently located on plasmids, facilitating their spread among bacteria.
- Current plasmid analysis methods are often limited, costly, or difficult to implement in resource-limited environments.
Purpose of the Study:
- To develop a simple, cost-effective assay for detecting antimicrobial resistance genes on bacterial plasmids.
- To provide a method suitable for low-resource settings to aid in AMR management.
Main Methods:
- Utilized CRISPR/Cas9 technology for targeted excision of antimicrobial resistance genes.
- Employed DNA combing for single-molecule imaging and detection of plasmid configuration changes (circular to linear).
- Visualized results using fluorescence microscopy.
Main Results:
- Successfully detected several β-lactamase-encoding genes on plasmids from clinical samples.
- The assay accurately identified the presence, number, and size of plasmids.
- Demonstrated the assay's feasibility using standard laboratory equipment.
Conclusions:
- The developed CRISPR/Cas9 excision and DNA combing assay is a rapid, inexpensive, and informative tool for plasmid analysis.
- This method is well-suited for low-resource settings, offering a practical approach to detect AMR genes.
- The assay aids in characterizing plasmids and managing antimicrobial resistance, particularly during outbreaks.

