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Plasmid-encoded trimethoprim resistance in staphylococci
Abstract:
High-level (greater than 1,000 micrograms/ml) resistance to the antimicrobial agent trimethoprim was found in 17 of 101 (17%) coagulase-negative staphylococci and 5 of 51 (10%) Staphylococcus aureus from a number of different hospitals in the United States. Resistance was plasmid encoded and could be transferred by conjugation in 4 of the 17 (24%) Tpr coagulase-negative staphylococci and 3 of the 5 (60%) Tpr S. aureus. A 1.2-kilobase segment of plasmid DNA from one of the plasmids (pG01) was cloned on a high-copy-number vector in Escherichia coli and expressed high-level Tpr (MIC, 1,025 micrograms/ml) in the gram-negative host. In situ filter hybridization demonstrated homology between the cloned Tpr gene probe and plasmid DNA from each conjugative Tpr plasmid, a single nonconjugative plasmid from a United States Staphylococcus epidermidis isolate, a nonconjugative plasmid from an Australian methicillin-resistant S. aureus isolate, and chromosomal DNA from three Tpr S. epidermidis isolates that did not contain any plasmid DNA that was homologous with the probe. No homology was seen between the probe and staphylococcal plasmids not mediating Tpr, plasmid DNA from 12 Tpr S. epidermidis isolates not transferring Tpr by conjugation, or plasmid-encoded Tpr genes derived from gram-negative bacteria. Plasmid-encoded Tpr appears to be a relatively new gene in staphylococci and, because it can be transferred by conjugation, could become more prevalent in nonsocomial isolates.
Insights
High-level trimethoprim resistance is emerging in staphylococci, often plasmid-encoded and transferable. This antimicrobial resistance gene may spread in hospital-acquired infections due to its conjugative nature.
Area of Science:
- Microbiology
- Molecular Biology
- Antimicrobial Resistance
Background:
- High-level trimethoprim resistance (Tpr) was observed in coagulase-negative staphylococci and Staphylococcus aureus in US hospitals.
- Resistance was frequently plasmid-encoded and transferable via conjugation in these staphylococcal isolates.
Purpose of the Study:
- To investigate the genetic basis and prevalence of trimethoprim resistance in staphylococci.
- To determine the transferability and potential spread of trimethoprim resistance genes.
Main Methods:
- Prevalence screening of trimethoprim resistance in staphylococcal isolates.
- Plasmid DNA analysis, conjugation experiments, and gene cloning.
- DNA hybridization techniques to identify homologous sequences.
Main Results:
- 17% of coagulase-negative staphylococci and 10% of S. aureus exhibited high-level trimethoprim resistance.
- Trimethoprim resistance genes were transferable in a significant proportion of resistant isolates.
- A cloned 1.2-kilobase DNA segment conferred high-level trimethoprim resistance in E. coli, confirming its role.
- Homology was found with various staphylococcal plasmids and chromosomal DNA, but not with gram-negative Tpr genes.
Conclusions:
- Plasmid-encoded trimethoprim resistance is a significant finding in staphylococci.
- The conjugative nature of these resistance genes suggests a potential for increased prevalence in nosocomial infections.
- This represents a relatively new threat in staphylococcal antimicrobial resistance.