Amplification of a section of chromosomal DNA in methicillin-resistant Staphylococcus aureus following growth in high concentrations of methicillin
- PMID: 3221194
- DOI: 10.1099/00221287-134-6-1455
Amplification of a section of chromosomal DNA in methicillin-resistant Staphylococcus aureus following growth in high concentrations of methicillin
Abstract
Growth of two independently isolated strains of methicillin-resistant Staphylococcus aureus (MRSA) in increasing concentrations of methicillin (step-selection) resulted in increased resistance in these strains. When chromosomal DNA from the step-selected variants was probed using DNA sequences previously demonstrated to be associated with methicillin resistance in MRSA strains, amplification of the homologous chromosomal sequence was identified. Growth of these step-selected strains in the absence of methicillin resulted in loss of the amplified sequence, while the original sequence remained. There are differences between the two strains in the stability of maintenance of amplified sections. Prolonged storage of the variants on a high concentration of methicillin resulted in loss of amplified sections without concomitant loss of methicillin resistance. Thus amplification may be only one of at least two molecular mechanisms available to S. aureus to increase methicillin resistance in response to step-selection. Probing of cells of the highly resistant sub-population of a heterogeneously resistant MRSA strain showed that duplication of this mec-associated DNA is not involved in the mechanism of heteroresistance.
Similar articles
-
The expression in Staphylococcus aureus of cloned DNA encoding methicillin resistance.J Gen Microbiol. 1988 Jun;134(6):1465-9. doi: 10.1099/00221287-134-6-1465. J Gen Microbiol. 1988. PMID: 3221195
-
The cloning of chromosomal DNA associated with methicillin and other resistances in Staphylococcus aureus.J Gen Microbiol. 1987 Jul;133(7):1919-29. doi: 10.1099/00221287-133-7-1919. J Gen Microbiol. 1987. PMID: 3668502
-
Restriction maps of the regions coding for methicillin and tobramycin resistances on chromosomal DNA in methicillin-resistant staphylococci.Antimicrob Agents Chemother. 1989 Sep;33(9):1624-6. doi: 10.1128/AAC.33.9.1624. Antimicrob Agents Chemother. 1989. PMID: 2817861 Free PMC article.
-
Additional DNA in methicillin-resistant Staphylococcus aureus and molecular cloning of mec-specific DNA.J Bacteriol. 1986 Feb;165(2):373-8. doi: 10.1128/jb.165.2.373-378.1986. J Bacteriol. 1986. PMID: 3003024 Free PMC article.
-
Methicillin-resistant staphylococci.Clin Microbiol Rev. 1988 Apr;1(2):173-86. doi: 10.1128/CMR.1.2.173. Clin Microbiol Rev. 1988. PMID: 3069195 Free PMC article. Review.
Cited by
-
Competing for Iron: Duplication and Amplification of the isd Locus in Staphylococcus lugdunensis HKU09-01 Provides a Competitive Advantage to Overcome Nutritional Limitation.PLoS Genet. 2016 Aug 30;12(8):e1006246. doi: 10.1371/journal.pgen.1006246. eCollection 2016 Aug. PLoS Genet. 2016. PMID: 27575058 Free PMC article.
-
Intra- and interpopulation transposition of mobile genetic elements driven by antibiotic selection.Nat Ecol Evol. 2022 May;6(5):555-564. doi: 10.1038/s41559-022-01705-2. Epub 2022 Mar 28. Nat Ecol Evol. 2022. PMID: 35347261
-
Bacterial gene amplification: implications for the evolution of antibiotic resistance.Nat Rev Microbiol. 2009 Aug;7(8):578-88. doi: 10.1038/nrmicro2174. Nat Rev Microbiol. 2009. PMID: 19609259 Review.
-
The Staphylococcus aureus mec determinant comprises an unusual cluster of direct repeats and codes for a gene product similar to the Escherichia coli sn-glycerophosphoryl diester phosphodiesterase.J Bacteriol. 1991 Dec;173(23):7416-22. doi: 10.1128/jb.173.23.7416-7422.1991. J Bacteriol. 1991. PMID: 1718947 Free PMC article.
-
Role for tandem duplication and lon protease in AcrAB-TolC- dependent multiple antibiotic resistance (Mar) in an Escherichia coli mutant without mutations in marRAB or acrRAB.J Bacteriol. 2006 Jun;188(12):4413-23. doi: 10.1128/JB.01502-05. J Bacteriol. 2006. PMID: 16740948 Free PMC article.