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Updated: Jul 14, 2026

Site-specific Bacterial Chromosome Engineering: ΦC31 Integrase Mediated Cassette Exchange (IMCE)
Published on: March 16, 2012
pRMH760, a precursor of A/C₂ plasmids carrying blaCMY and blaNDM genes
Christopher J Harmer1, Ruth M Hall
1School of Molecular Bioscience, The University of Sydney , Sydney, Australia .
Abstract:
To investigate the evolution of plasmids in the repA/C2 group carrying genes conferring resistance to cephalosporins (bla(CMY)) or to carbapenems (bla(NDM)) and cephalosporins (bla(CMY)), the sequence of plasmid pRMH760 that lacks the β-lactamase genes was determined and compared to all available A/C2 plasmid sequences. pRMH760 is 170.6 kb and carries several antibiotic resistance genes in a 45.1 kb complex transposon structure located upstream of the rhs gene. In plasmid pR148, the closest relative of pRMH760, the antibiotic resistance island is in the same position but the resistance genes differ. pRMH760 also contains a deletion in the rhs gene. Sequenced A/C2 plasmids containing bla(CMY) or bla(CMY) and bla(NDM) have backbones closely related to the pRMH760/pR148 backbone, and they include resistance islands in the same location, indicating that they arose from a plasmid related to pRMH760/pR148. However, the gene content of this resistance island differs in each case, and the island family was designated ARI-A. The bla(NDM) gene is within ARI-A. The ISEcp1-bla(CMY) fragment is located elsewhere and is always in the same location, consistent with a single acquisition event. Plasmids containing only bla(CMY) carry a second resistance island, designated ARI-B, which includes the sul2 gene and a variable set of further resistance genes. Nine A/C2 plasmids that were not of this type (type 1) were found to have a similar backbone that can be simply distinguished by the presence of two exchanged regions and two insertions. Antibiotic resistance islands in type 2 plasmids are in different locations and have different structures.
Insights
The evolution of repA/C2 plasmids carrying cephalosporin and carbapenem resistance genes was studied. These plasmids share a common backbone, with resistance genes located in distinct mobile genetic elements.
Area of Science:
- Molecular Biology
- Genetics
- Microbiology
Background:
- Plasmids are key vehicles for antibiotic resistance gene dissemination.
- The repA/C2 group of plasmids carries genes for resistance to critical antibiotics like cephalosporins and carbapenems.
- Understanding plasmid evolution is crucial for combating antimicrobial resistance.
Purpose of the Study:
- To investigate the evolutionary history of repA/C2 plasmids.
- To characterize the genetic structures associated with cephalosporin (blaCMY) and carbapenem (blaNDM) resistance genes on these plasmids.
- To compare plasmid backbones and resistance island arrangements.
Main Methods:
- Whole-genome sequencing of plasmid pRMH760.
- Comparative sequence analysis of pRMH760 against other available A/C2 plasmid sequences.
- Identification and characterization of antibiotic resistance islands (ARIs).
Main Results:
- Plasmids carrying blaCMY or blaCMY/blaNDM share a common backbone related to pRMH760/pR148.
- Antibiotic resistance genes are located in mobile genetic elements, designated ARI-A (containing blaNDM) and ARI-B (containing sul2).
- The ISEcp1-blaCMY fragment appears to be acquired via a single event, while ARI-A and ARI-B show variability.
Conclusions:
- RepA/C2 plasmids with blaCMY and/or blaNDM evolved from a common ancestral plasmid.
- The modular structure of antibiotic resistance islands facilitates their acquisition and diversification.
- Understanding plasmid evolution aids in tracking and controlling the spread of antibiotic resistance.

