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RmtC and RmtF 16S rRNA Methyltransferase in NDM-1-Producing Pseudomonas aeruginosa
Abstract:
We investigated 16S rRNA methyltransferases in 38 blaNDM-1-positive Pseudomonas aeruginosa isolates and found RmtC in 3 isolates, 1 of which also harbored RmtF. The isolates were clonally unrelated; rmtC and rmtF genes were located on a chromosome with the blaNDM-1 gene. Strategies are needed to limit the spread of such isolates.
Insights
We found 16S rRNA methyltransferases RmtC and RmtF in Pseudomonas aeruginosa isolates carrying the blaNDM-1 gene. These resistance genes were located on the chromosome, highlighting the need for strategies to limit the spread of these resistant bacteria.
Area of Science:
- Microbiology
- Genetics
- Antimicrobial Resistance
Background:
- Pseudomonas aeruginosa is an opportunistic pathogen.
- The blaNDM-1 gene confers resistance to carbapenem antibiotics.
- 16S rRNA methyltransferases are enzymes that confer high-level aminoglycoside resistance.
Purpose of the Study:
- To investigate the presence and location of 16S rRNA methyltransferases in blaNDM-1-positive Pseudomonas aeruginosa isolates.
- To understand the genetic context of these resistance genes.
Main Methods:
- Screening of 38 blaNDM-1-positive Pseudomonas aeruginosa isolates for 16S rRNA methyltransferases.
- Gene localization studies (chromosomal vs. plasmid).
Main Results:
- RmtC was detected in 3 isolates.
- One isolate harbored both RmtC and RmtF.
- The rmtC and rmtF genes were found to be chromosomally located alongside the blaNDM-1 gene.
- The 38 isolates were determined to be clonally unrelated.
Conclusions:
- The co-location of blaNDM-1, rmtC, and rmtF on the chromosome of clonally distinct Pseudomonas aeruginosa isolates is a significant finding.
- This suggests independent acquisition events or efficient chromosomal integration mechanisms.
- Effective strategies are crucial to curb the dissemination of these multidrug-resistant isolates.
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