Genetic basis of multidrug resistance in Acinetobacter baumannii clinical isolates at a tertiary medical center in Pennsylvania

Jennifer M. Adams-Haduch, David L. Paterson, Hanna E. Sidjabat, Anthony W. Pasculle, Brian A. Potoski, Carlene A. Muto, Lee H. Harrison, Yohei Doi

Research output: Contribution to journalArticle

105 Citations (Scopus)

Abstract

A total of 49 unique clinical isolates of multidrug-resistant (MDR) Acinetobacter baumannii identified at a tertiary medical center in Pittsburgh, Pennsylvania, between August 2006 and September 2007 were studied for the genetic basis of their MDR phenotype. Approximately half of all A. baumannii clinical isolates identified during this period qualified as MDR, defined by nonsusceptibility to three or more of the antimicrobials routinely tested in the clinical microbiology laboratory. Among the MDR isolates, 18.4% were resistant to imipenem. The frequencies of resistance to amikacin and ciprofloxacin were high at 36.7% and 95.9%, respectively. None of the isolates was resistant to colistin or tigecycline. The presence of the carbapenemase gene bla OXA-23 and the 16S rRNA methylase gene armA predicted high-level resistance to imipenem and amikacin, respectively. blaOXA-23 was preceded by insertion sequence ISAba1, which likely provided a potent promoter activity for the expression of the carbapenemase gene. The structure of the transposon defined by ISAba1 differed from those reported in Europe, suggesting that ISAba1-mediated acquisition of blaOXA-23 may occur as an independent event. Typical substitutions in the quinolone resistance-determining regions of the gyrA and parC genes were observed in the ciprofloxacin-resistant isolates. Plasmid-mediated quinolone resistance genes, including the qnr genes, were not identified. Fifty-nine percent of the MDR isolates belonged to a single clonal group over the course of the study period, as demonstrated by pulsed-field gel electrophoresis.

Original languageEnglish
Pages (from-to)3837-3843
Number of pages7
JournalAntimicrobial agents and chemotherapy
Volume52
Issue number11
DOIs
Publication statusPublished - 01-11-2008

Fingerprint

Acinetobacter baumannii
Multiple Drug Resistance
Amikacin
Imipenem
Quinolones
Ciprofloxacin
Genes
Colistin
Insertional Mutagenesis
Pulsed Field Gel Electrophoresis
Microbiology
rRNA Genes
Plasmids
Phenotype
Gene Expression
carbapenemase

All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

Cite this

Adams-Haduch, Jennifer M. ; Paterson, David L. ; Sidjabat, Hanna E. ; Pasculle, Anthony W. ; Potoski, Brian A. ; Muto, Carlene A. ; Harrison, Lee H. ; Doi, Yohei. / Genetic basis of multidrug resistance in Acinetobacter baumannii clinical isolates at a tertiary medical center in Pennsylvania. In: Antimicrobial agents and chemotherapy. 2008 ; Vol. 52, No. 11. pp. 3837-3843.
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Adams-Haduch, JM, Paterson, DL, Sidjabat, HE, Pasculle, AW, Potoski, BA, Muto, CA, Harrison, LH & Doi, Y 2008, 'Genetic basis of multidrug resistance in Acinetobacter baumannii clinical isolates at a tertiary medical center in Pennsylvania', Antimicrobial agents and chemotherapy, vol. 52, no. 11, pp. 3837-3843. https://doi.org/10.1128/AAC.00570-08

Genetic basis of multidrug resistance in Acinetobacter baumannii clinical isolates at a tertiary medical center in Pennsylvania. / Adams-Haduch, Jennifer M.; Paterson, David L.; Sidjabat, Hanna E.; Pasculle, Anthony W.; Potoski, Brian A.; Muto, Carlene A.; Harrison, Lee H.; Doi, Yohei.

In: Antimicrobial agents and chemotherapy, Vol. 52, No. 11, 01.11.2008, p. 3837-3843.

Research output: Contribution to journalArticle

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T1 - Genetic basis of multidrug resistance in Acinetobacter baumannii clinical isolates at a tertiary medical center in Pennsylvania

AU - Adams-Haduch, Jennifer M.

AU - Paterson, David L.

AU - Sidjabat, Hanna E.

AU - Pasculle, Anthony W.

AU - Potoski, Brian A.

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AU - Harrison, Lee H.

AU - Doi, Yohei

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N2 - A total of 49 unique clinical isolates of multidrug-resistant (MDR) Acinetobacter baumannii identified at a tertiary medical center in Pittsburgh, Pennsylvania, between August 2006 and September 2007 were studied for the genetic basis of their MDR phenotype. Approximately half of all A. baumannii clinical isolates identified during this period qualified as MDR, defined by nonsusceptibility to three or more of the antimicrobials routinely tested in the clinical microbiology laboratory. Among the MDR isolates, 18.4% were resistant to imipenem. The frequencies of resistance to amikacin and ciprofloxacin were high at 36.7% and 95.9%, respectively. None of the isolates was resistant to colistin or tigecycline. The presence of the carbapenemase gene bla OXA-23 and the 16S rRNA methylase gene armA predicted high-level resistance to imipenem and amikacin, respectively. blaOXA-23 was preceded by insertion sequence ISAba1, which likely provided a potent promoter activity for the expression of the carbapenemase gene. The structure of the transposon defined by ISAba1 differed from those reported in Europe, suggesting that ISAba1-mediated acquisition of blaOXA-23 may occur as an independent event. Typical substitutions in the quinolone resistance-determining regions of the gyrA and parC genes were observed in the ciprofloxacin-resistant isolates. Plasmid-mediated quinolone resistance genes, including the qnr genes, were not identified. Fifty-nine percent of the MDR isolates belonged to a single clonal group over the course of the study period, as demonstrated by pulsed-field gel electrophoresis.

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