Population-level transition of capsular polysaccharide types among sequence type 1 group B Streptococcus isolates

Noriyuki Nagano1, Shota Koide1, Wataru Hayashi1

  • 1Department of Health and Medical Sciences, Shinshu University Graduate School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.

Insights

Group B Streptococcus isolates with reduced penicillin susceptibility (PRGBS) in elderly patients showed shifting serotypes over 35 months. Genetic analysis revealed capsular switching and nosocomial transmission may drive these population-level serotype replacements in ST1 PRGBS.

Area of Science:

  • Microbiology
  • Genetics
  • Epidemiology

Background:

  • Group B Streptococcus (GBS) can cause serious infections, particularly in elderly patients.
  • Reduced penicillin susceptibility in GBS (PRGBS) is an emerging concern.
  • Understanding serotype dynamics and genetic relatedness of PRGBS is crucial for infection control.

Purpose of the Study:

  • To investigate the population-level transition of PRGBS serotypes in elderly patients over a 35-month period.
  • To analyze the genetic relatedness and genomic features of PRGBS isolates.
  • To explore potential mechanisms driving serotype replacement.

Main Methods:

  • Retrospective analysis of 77 non-duplicate PRGBS isolates from 73 elderly patients.
  • Serotyping of isolates.
  • Analysis of genetic relatedness using whole-genome sequencing (WGS).
  • Investigation of specific genetic elements, including cps gene clusters and flanking regions.

Main Results:

  • A significant shift in PRGBS serotypes was observed: Serotype III predominated initially, followed by transient serotype Ib, then predominantly serotype Ia, with a resurgence of serotype III.
  • Serotype III and Ia isolates belonged to Sequence Type 1 (ST1) and shared key substitutions in penicillin-binding protein 2X.
  • WGS revealed genomic similarities between serotype III and Ia strains, with distinct genetic alterations in capsular gene cluster flanking regions (e.g., IS1548 insertion in serotype III, ΔISSag8 in serotype Ia).
  • The re-emergence of serotype III in the later period was associated with the tRNA-Arg-ΔISSag8-rpsA region.

Conclusions:

  • Capsular switching and potential nosocomial transmission are likely drivers of population-level serotype replacement among ST1 PRGBS isolates.
  • The study highlights the dynamic nature of PRGBS epidemiology and the importance of ongoing surveillance.
  • Genetic modifications in flanking regions of the cps gene cluster may play a role in serotype evolution and adaptation.

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