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Antibiotic resistance in invasive Streptococcus pneumoniae isolates identified in Scotland between 1999 and 2007

Benjamin Cooke1, Andrew Smith2, Mathew Diggle3

  • 1Microbiology Department, Glasgow Royal Infirmary, Glasgow, UK.

Insights

Streptococcus pneumoniae susceptibility to penicillin and cefotaxime remained high in Scotland from 1999-2007. Erythromycin resistance was observed in 12% of isolates, primarily from serogroup 14.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background:

  • Invasive pneumococcal disease (IPD) poses a significant public health challenge.
  • Monitoring antimicrobial susceptibility patterns of Streptococcus pneumoniae is crucial for effective treatment.
  • The Scottish Haemophilus, Legionella, Meningococcus and Pneumococcus Reference Laboratory collects vital data on pneumococcal isolates.

Purpose of the Study:

  • To analyze antimicrobial susceptibility profiles of invasive Streptococcus pneumoniae isolates in Scotland.
  • To determine resistance trends to penicillin, erythromycin, and cefotaxime between 1999 and 2007.
  • To identify specific serogroups and clones associated with resistance patterns.

Main Methods:

  • Retrospective analysis of 4727 invasive Streptococcus pneumoniae isolates.
  • Determination of minimum inhibitory concentrations (MICs) for penicillin, erythromycin, and cefotaxime.
  • Serotyping and molecular typing of resistant isolates, including identification of internationally recognized clones.

Main Results:

  • Penicillin resistance remained low (0.2%), with sporadic isolates mainly from serogroup 14 (ST9) and 9 (ST156).
  • Erythromycin resistance was found in 12% of isolates, predominantly serogroup 14 (ST9).
  • Cefotaxime resistance was very low (0.06%). Internationally recognized clones predominated in resistant isolates.

Conclusions:

  • Susceptibility to key antimicrobial agents for invasive pneumococcal disease in Scotland remained high during 1999-2007.
  • Erythromycin resistance, particularly in serogroup 14, warrants continued surveillance.
  • The findings support the ongoing effectiveness of first-line treatments for IPD in the studied period.

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