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Vancomycin resistance is encoded on a pheromone response plasmid in Enterococcus faecium 228
S Handwerger1, M J Pucci, A Kolokathis
1Department of Medicine, Beth Israel Medical Center, Mount Sinai School of Medicine, New York, New York 10003.
Antimicrobial Agents and Chemotherapy
|February 1, 1990
Summary
A novel plasmid, pHKK100, from Enterococcus faecium 228 confers vancomycin resistance. This conjugative plasmid also enables pheromone response in other bacteria, a dual function previously undescribed.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Enterococcus faecium is a significant cause of hospital-acquired infections.
- Vancomycin resistance in enterococci is a growing public health concern.
- Conjugative plasmids play a crucial role in the dissemination of antibiotic resistance genes.
Purpose of the Study:
- To characterize the genetic basis of vancomycin resistance in Enterococcus faecium 228.
- To investigate the transferability and functional properties of the vancomycin resistance plasmid.
- To identify novel plasmid-mediated traits beyond antibiotic resistance.
Main Methods:
- Plasmid isolation and characterization (55-kilobase plasmid pHKK100 identified).
- Conjugative transfer experiments into susceptible Enterococcus faecalis strains.
- Assessment of pheromone response capabilities conferred by the plasmid.
Main Results:
- The vancomycin resistance determinant in E. faecium 228 resides on the conjugative plasmid pHKK100.
- pHKK100 was efficiently transferred to susceptible E. faecalis strains.
- Transconjugants acquired the ability to respond to pheromones produced by E. faecalis and Streptococcus sanguis.
Conclusions:
- pHKK100 is the first described plasmid mediating both vancomycin resistance and bacterial pheromone response.
- This dual functionality highlights the complex roles plasmids can play in bacterial adaptation and interspecies communication.
- Understanding such plasmids is critical for combating antibiotic resistance and its spread.