Literature DB >> 2838448

Multiresistant Staphylococcus aureus: genetics and evolution of epidemic Australian strains.

R A Skurray1, D A Rouch, B R Lyon, M T Gillespie, J M Tennent, M E Byrne, L J Messerotti, J W May.   

Abstract

Molecular and genetic analysis of multiresistant isolates of Staphylococcus aureus from widely separated hospitals in Australia has demonstrated that these are clearly related, and that the predominant strains possess up to three different plasmids, which fall into the following classes: (i) small 1.6 kb plasmids, such as pSK3, which are phenotypically cryptic, (ii) 4.5 kb chloramphenicol resistance plasmids, such as pSK2, and (iii) the pSK1 family of multiresistance plasmids, which range in size from 20 to 42 kb and variously encode resistance to antiseptics and disinfectants, trimethoprim (Tpr), penicillin (Pcr) and the aminoglycosides gentamicin, tobramycin and kanamycin (Gmr Tmr Kmr). Gmr Tmr Kmr is encoded on the pSK1 family plasmids by transposon Tn4001, which was also detected on the chromosomes of some clinical isolates. Tn4001 is composed of inverted repeats of the insertion sequence IS256; these repeats flank a Gmr Tmr Kmr sequence encoding for a 57,000 dalton bifunctional protein with aminoglycoside acetyltransferase [AAC(6')] and phosphotransferase [APH(2")] activities. A Tn4001-like structure, which is defective in transposition but encodes for a Gmr Tmr Kmr determinant homologous with that on Tn4001, occurs on conjugative plasmids from strains isolated in North America. Physical studies indicate that Pcr, via a beta-lactamase, and Tpr, via a trimethoprim-insensitive dihydrofolate reductase (DHFR), are also encoded on the pSK1 family by transposons; these transposons have been designated Tn4002 and Tn4003, respectively. Tn4003 is flanked by direct repeats of the insertion sequence IS257. The evolution of the pSK1 family of multiresistance plasmids is traced through the transposition and genetic rearrangement of resistance determinants. Transposition and genetic rearrangement have also contributed to the evolution of a multiresistant chromosome in Staph. aureus. In the majority of contemporary multiply resistant Staph. aureus strains the determinants for resistance to erythromycin (Emr), fusidic acid, methicillin (Mcr), minocycline, rifampicin, spectinomycin, streptomycin, sulphonamides, tetracycline (Tcr), cadmium (Cdr), and mercury (Hgr) are chromosomally encoded; these strains also possess chromosomally encoded Pcr, via a beta-lactamase. Evidence indicates that some of these determinants, Pcr, Cdr, Hgr, and Tcr, were plasmid encoded in isolates collected from Australian hospitals prior to 1970. Through transposition and site-specific integration, they have since been acquired by the chromosome in more recent Staph. aureus strains.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1988        PMID: 2838448     DOI: 10.1093/jac/21.suppl_c.19

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  12 in total

Review 1.  Molecular detection of antimicrobial resistance.

Authors:  A C Fluit; M R Visser; F J Schmitz
Journal:  Clin Microbiol Rev       Date:  2001-10       Impact factor: 26.132

Review 2.  Potential impact of increased use of biocides in consumer products on prevalence of antibiotic resistance.

Authors:  Peter Gilbert; Andrew J McBain
Journal:  Clin Microbiol Rev       Date:  2003-04       Impact factor: 26.132

Review 3.  Proton-dependent multidrug efflux systems.

Authors:  I T Paulsen; M H Brown; R A Skurray
Journal:  Microbiol Rev       Date:  1996-12

4.  Replication of staphylococcal multiresistance plasmids.

Authors:  N Firth; S Apisiridej; T Berg; B A O'Rourke; S Curnock; K G Dyke; R A Skurray
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

5.  Organization of the antiseptic resistance gene qacA and Tn552-related beta-lactamase genes in multidrug- resistant Staphylococcus haemolyticus strains of animal and human origins.

Authors:  I-L Anthonisen; M Sunde; T M Steinum; M S Sidhu; H Sørum
Journal:  Antimicrob Agents Chemother       Date:  2002-11       Impact factor: 5.191

Review 6.  Efflux-mediated drug resistance in bacteria.

Authors:  Xian-Zhi Li; Hiroshi Nikaido
Journal:  Drugs       Date:  2004       Impact factor: 9.546

7.  Conjugative transfer genes in staphylococcal isolates from the United States.

Authors:  G L Archer; J Scott
Journal:  Antimicrob Agents Chemother       Date:  1991-12       Impact factor: 5.191

8.  Molecular analysis of a gentamicin resistance transposonlike element on plasmids isolated from North American Staphylococcus aureus strains.

Authors:  M E Byrne; M T Gillespie; R A Skurray
Journal:  Antimicrob Agents Chemother       Date:  1990-11       Impact factor: 5.191

9.  An Efficient Synthesis of 3-Alkylpyridine Alkaloids Enables Their Biological Evaluation.

Authors:  Anna R Kaplan; Cassandra L Schrank; William M Wuest
Journal:  ChemMedChem       Date:  2021-04-14       Impact factor: 3.540

10.  Remodeling of pSK1 Family Plasmids and Enhanced Chlorhexidine Tolerance in a Dominant Hospital Lineage of Methicillin-Resistant Staphylococcus aureus.

Authors:  Sarah L Baines; Slade O Jensen; Neville Firth; Anders Gonçalves da Silva; Torsten Seemann; Glen P Carter; Deborah A Williamson; Benjamin P Howden; Timothy P Stinear
Journal:  Antimicrob Agents Chemother       Date:  2019-04-25       Impact factor: 5.191

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