Clonal Distribution, Antimicrobial Resistance, and Pilus Islets in S. pneumoniae Isolates from PCV10-Vaccinated

Alexandra Sashova Alexandrova1, Daniela Rosenova Pencheva2, Ivan Gergov Mitov1

  • 1Department of Medical Microbiology, Medical Faculty, Medical University of Sofia, Bulgaria.

Insights

Despite pneumococcal conjugate vaccines (PCVs), Streptococcus pneumoniae remains a major cause of acute otitis media (AOM). This study found high rates of antibiotic non-susceptibility and multidrug resistance in S. pneumoniae isolates from vaccinated children in Bulgaria.

Area of Science:

  • Microbiology
  • Epidemiology
  • Vaccinology

Background:

  • Streptococcus pneumoniae is a primary bacterial cause of acute otitis media (AOM).
  • Pneumococcal conjugate vaccines (PCVs) aim to reduce AOM incidence, but pathogen evolution necessitates ongoing surveillance.
  • Understanding the population dynamics of S. pneumoniae in vaccinated populations is crucial for public health.

Purpose of the Study:

  • To investigate the population structure, antibiotic resistance, serotype distribution, and pilus presence of S. pneumoniae isolates from PCV10-vaccinated children with AOM in Bulgaria.
  • To identify associations between clonal complexes, serotypes, and antimicrobial resistance patterns.
  • To inform future vaccine strategies and antimicrobial stewardship.

Main Methods:

  • Analysis of middle ear fluid S. pneumoniae isolates from PCV10-vaccinated children.
  • Determination of antibiotic non-susceptibility and multidrug resistance (MDR).
  • Serotyping, pilus typing, and multilocus sequence typing (MLST) to define clonal complexes (CCs).

Main Results:

  • High rates of antibiotic non-susceptibility (68.75%) and MDR (60.4%) were observed.
  • Predominant serotypes included non-PCV10 types 3, 19A, and VT 19F, with 64.6% being non-PCV10 serotypes.
  • Four main clonal complexes (CCs) were identified: CC320 (39.6%), CC505 (12.5%), CC1377 (8.3%), and CC230 (8.3%), with strong associations between CCs, serotypes, and resistance.

Conclusions:

  • PCV10 vaccination did not fully prevent AOM caused by S. pneumoniae, with a significant proportion of non-vaccine serotypes and high antimicrobial resistance.
  • Specific clonal complexes, notably CC320, are associated with multidrug resistance and prevalent serotypes.
  • Continuous monitoring of vaccine-induced changes in S. pneumoniae antimicrobial resistance and clonality is essential.

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