Plasmid-encoded trimethoprim resistance in staphylococci
- PMID: 3729338
- PMCID: PMC284144
- DOI: 10.1128/AAC.29.5.733
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.
Similar articles
-
Molecular epidemiology of trimethoprim resistance among coagulase-negative staphylococci.Antimicrob Agents Chemother. 1987 Nov;31(11):1683-8. doi: 10.1128/AAC.31.11.1683. Antimicrob Agents Chemother. 1987. PMID: 3435115 Free PMC article.
-
Molecular analyses of conjugative, gentamicin-resistance plasmids from staphylococcal clinical isolates.Can J Microbiol. 1988 Sep;34(9):1050-7. doi: 10.1139/m88-185. Can J Microbiol. 1988. PMID: 3214809
-
Trimethoprim resistance determinants encoding a dihydrofolate reductase in clinical isolates of Staphylococcus aureus and coagulase-negative staphylococci.J Med Microbiol. 1988 May;26(1):67-73. doi: 10.1099/00222615-26-1-67. J Med Microbiol. 1988. PMID: 3373516
-
[Molecular biological characteristics of staphylococcal plasmids].Antibiotiki. 1984 Feb;29(2):148-54. Antibiotiki. 1984. PMID: 6367632 Review. Russian. No abstract available.
-
Multiresistant Staphylococcus aureus: genetics and evolution of epidemic Australian strains.J Antimicrob Chemother. 1988 Apr;21 Suppl C:19-39. doi: 10.1093/jac/21.suppl_c.19. J Antimicrob Chemother. 1988. PMID: 2838448 Review.
Cited by
-
An accessory protein is required for relaxosome formation by small staphylococcal plasmids.J Bacteriol. 2004 Jun;186(11):3363-73. doi: 10.1128/JB.186.11.3363-3373.2004. J Bacteriol. 2004. PMID: 15150221 Free PMC article.
-
Cloning and characterization of a novel, plasmid-encoded trimethoprim-resistant dihydrofolate reductase from Staphylococcus haemolyticus MUR313.Antimicrob Agents Chemother. 1995 Sep;39(9):1920-4. doi: 10.1128/AAC.39.9.1920. Antimicrob Agents Chemother. 1995. PMID: 8540692 Free PMC article.
-
Towards the understanding of resistance mechanisms in clinically isolated trimethoprim-resistant, methicillin-resistant Staphylococcus aureus dihydrofolate reductase.J Struct Biol. 2010 Apr;170(1):93-7. doi: 10.1016/j.jsb.2009.12.011. Epub 2009 Dec 21. J Struct Biol. 2010. PMID: 20026215 Free PMC article.
-
Plasmid-mediated trimethoprim-resistance in Staphylococcus aureus. Characterization of the first gram-positive plasmid dihydrofolate reductase (type S1).Biochem J. 1987 Apr 1;243(1):309-12. doi: 10.1042/bj2430309. Biochem J. 1987. PMID: 3606580 Free PMC article.
-
Antimicrobial resistance of Staphylococcus aureus: genetic basis.Microbiol Rev. 1987 Mar;51(1):88-134. doi: 10.1128/mr.51.1.88-134.1987. Microbiol Rev. 1987. PMID: 3031442 Free PMC article. Review. No abstract available.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources