Literature DB >> 2729941

Antimicrobial resistance in nosocomial isolates of Staphylococcus haemolyticus.

J W Froggatt1, J L Johnston, D W Galetto, G L Archer.   

Abstract

Staphylococcus haemolyticus is frequently cultured from hospitalized patients and is characterized by resistance to multiple antimicrobial agents. We found that S. haemolyticus represented 70 of 524 (13%) coagulase-negative staphylococcal isolates identified by the clinical microbiology laboratories of two hospitals over 2 months. S. haemolyticus isolates were recovered from wounds (44%), urine (26%), blood (10%), and other sources (20%). All S. haemolyticus isolates were tested for susceptibility to six antimicrobial agents; 77% were resistant to three or more agents, and 41% were resistant to five or six agents. In addition, among 47 multiply resistant isolates, high MICs (greater than or equal to 6.25 micrograms/ml) of vancomycin (62% of isolates) and teicoplanin (91% of isolates) were found. DNA probes which were derived from S. epidermidis or S. aureus and which contained sequences associated with resistance to antimicrobial agents were used to detect specific genes in the total cellular and plasmid DNAs of 10 resistant S. haemolyticus isolates. Resistance gene probes and the numbers of resistant isolates hybridizing were as follows: methicillin, 10 of 10; gentamicin, 9 of 10; erythromycin, 7 of 10; and trimethoprim, 0 of 10. Genes for resistance to methicillin were found only in chromosomal locations, genes for resistance to gentamicin were found in both chromosomal and plasmid locations, and genes for resistance to erythromycin were found in plasmid locations only. With the exception of trimethoprim resistance determinants, similar genes were found among concurrently isolated multiply resistant S. epidermidis isolates from our hospitals. S. haemolyticus is a potentially important nosocomial species which readily acquires antimicrobial resistance genes and which shares, to some extent, in a common gene pool with S. epidermidis.

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Year:  1989        PMID: 2729941      PMCID: PMC172460          DOI: 10.1128/AAC.33.4.460

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  32 in total

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Journal:  N Engl J Med       Date:  1987-04-09       Impact factor: 91.245

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Journal:  J Hosp Infect       Date:  1986-03       Impact factor: 3.926

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Journal:  Zentralbl Bakteriol Mikrobiol Hyg A       Date:  1985-08

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Authors:  B R Lyon; M T Gillespie; M E Byrne; J W May; R A Skurray
Journal:  J Med Microbiol       Date:  1987-03       Impact factor: 2.472

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Journal:  J Clin Microbiol       Date:  1985-03       Impact factor: 5.948

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Journal:  J Bacteriol       Date:  1986-02       Impact factor: 3.490

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Journal:  J Antimicrob Chemother       Date:  1984-08       Impact factor: 5.790

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Journal:  Am J Clin Pathol       Date:  1986-01       Impact factor: 2.493

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Authors:  J M Hamilton-Miller; A Iliffe
Journal:  J Med Microbiol       Date:  1985-04       Impact factor: 2.472

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  67 in total

1.  Identical genes confer high-level resistance to gentamicin upon Enterococcus faecalis, Enterococcus faecium, and Streptococcus agalactiae.

Authors:  A Kaufhold; A Podbielski; T Horaud; P Ferrieri
Journal:  Antimicrob Agents Chemother       Date:  1992-06       Impact factor: 5.191

2.  Purification and characterization of recombinant Staphylococcus haemolyticus DNA gyrase and topoisomerase IV expressed in Escherichia coli.

Authors:  Joel C Bronstein; Stacey L Olson; Kristin LeVier; Mark Tomilo; Peter C Weber
Journal:  Antimicrob Agents Chemother       Date:  2004-07       Impact factor: 5.191

3.  In vitro activities of three semisynthetic amide derivatives of teicoplanin, MDL 62208, MDL 62211, and MDL 62873.

Authors:  F Biavasco; R Lupidi; P E Varaldo
Journal:  Antimicrob Agents Chemother       Date:  1992-02       Impact factor: 5.191

4.  Antimicrobial activity of MDL 62,873, a semisynthetic derivative of teicoplanin, in vitro and in experimental infections.

Authors:  M Berti; G Candiani; M Borgonovi; P Landini; F Ripamonti; R Scotti; L Cavenaghi; M Denaro; B P Goldstein
Journal:  Antimicrob Agents Chemother       Date:  1992-02       Impact factor: 5.191

5.  Staphylococcus haemolyticus as an important hospital pathogen and carrier of methicillin resistance genes.

Authors:  E M Barros; H Ceotto; M C F Bastos; K R N Dos Santos; M Giambiagi-Demarval
Journal:  J Clin Microbiol       Date:  2011-10-05       Impact factor: 5.948

6.  In vitro selection of resistance to vancomycin in bloodstream isolates of Staphylococcus haemolyticus and Staphylococcus epidermidis.

Authors:  L Herwaldt; L Boyken; M Pfaller
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1991-12       Impact factor: 3.267

7.  Mobility of gentamicin resistance genes from staphylococci isolated in the United States: identification of Tn4031, a gentamicin resistance transposon from Staphylococcus epidermidis.

Authors:  W D Thomas; G L Archer
Journal:  Antimicrob Agents Chemother       Date:  1989-08       Impact factor: 5.191

8.  DNA sequence and units of transcription of the conjugative transfer gene complex (trs) of Staphylococcus aureus plasmid pGO1.

Authors:  T M Morton; D M Eaton; J L Johnston; G L Archer
Journal:  J Bacteriol       Date:  1993-07       Impact factor: 3.490

9.  Biofilm formation by Staphylococcus haemolyticus.

Authors:  Elizabeth Gladys Aarag Fredheim; Claus Klingenberg; Holger Rohde; Stephanie Frankenberger; Peter Gaustad; Trond Flaegstad; Johanna Ericson Sollid
Journal:  J Clin Microbiol       Date:  2009-01-14       Impact factor: 5.948

10.  Detection of contamination during organ culture of the human cornea.

Authors:  Martin Hermel; Sabine Salla; Nicole Hamsley; André Steinfeld; Peter Walter
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2009-09-23       Impact factor: 3.117

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