Fluoroquinolone resistance in clinical isolates of Streptococcus pneumoniae from Asian countries: ANSORP study

Won Sup Oh1, Ji Yoeun Suh, Jae-Hoon Song

  • 1Samsung Medical Centre, Sungkyunkwan University School of Medicine, Seoul, Korea.

Microbial Drug Resistance (Larchmont, N.Y.)
|May 14, 2004
PubMed

Insights

Reduced susceptibility to ciprofloxacin in Streptococcus pneumoniae is linked to multiple genetic mutations. Specific alterations in gyrA, gyrB, parC, and parE genes contribute to fluoroquinolone resistance in these bacterial isolates.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Streptococcus pneumoniae is a leading cause of bacterial pneumonia and meningitis.
  • Fluoroquinolone antibiotics are crucial for treating pneumococcal infections.
  • Emergence of fluoroquinolone resistance in S. pneumoniae poses a significant public health threat.

Purpose of the Study:

  • To investigate the genetic mechanisms underlying reduced susceptibility to ciprofloxacin in clinical isolates of Streptococcus pneumoniae from Asia.
  • To identify specific mutations in quinolone resistance-determining regions (QRDRs) associated with fluoroquinolone resistance.

Main Methods:

  • Antimicrobial susceptibility testing was performed on 17 clinical isolates.
  • Serotyping and pulsed-field gel electrophoresis (PFGE) were used for molecular characterization.
  • DNA sequencing of gyrA, gyrB, parC, and parE genes was conducted to identify mutations in QRDRs.

Main Results:

  • All but one isolate exhibited multiple amino acid alterations in the QRDRs of gyrA, gyrB, parC, and parE.
  • Ile460 --> Val in parE was the most frequent mutation.
  • Specific mutations, such as Lys137 --> Asn in parC and Ser81 --> Phe in gyrA, were associated with high-level fluoroquinolone resistance.
  • Two novel mutations in gyrB (Ala390 --> Val and Asn423 --> Thr) were identified.
  • PFGE suggested the local spread of a multidrug-resistant Spain(23F)-1 clone in Hong Kong.

Conclusions:

  • Multiple genetic mutations in QRDRs are responsible for reduced ciprofloxacin susceptibility in S. pneumoniae.
  • Specific mutations in parC and gyrA play key roles in developing high-level and multidrug resistance.
  • The Spain(23F)-1 clone may be spreading in Hong Kong, necessitating further surveillance.

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