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Published on: February 23, 2014
Evolving genomic landscape of pediatric pneumococcus in two Canadian urban centers following conjugate vaccination
Sarah Teatero1, Allison McGeer2,3, Agron Plevneshi2
1Public Health Ontario, Toronto, ON, Canada.
Insights
Pneumococcal conjugate vaccines (PCVs) reduced disease but led to new serotypes and antimicrobial resistance. Ongoing genomic surveillance is crucial for monitoring these evolving trends in pediatric invasive pneumococcal disease (IPD).
Area of Science:
- Microbiology
- Epidemiology
- Genomics
Background:
- Pneumococcal conjugate vaccines (PCVs) have decreased pediatric invasive pneumococcal disease (IPD).
- Concerns persist regarding vaccine escape variants, emergence of non-vaccine serotypes (NVTs), and antimicrobial resistance (AMR).
Purpose of the Study:
- To analyze long-term trends in serotype distribution, lineage composition, and AMR patterns of pediatric IPD.
- Focus on Calgary and Toronto, Canada, post-PCV introduction.
Main Methods:
- Whole-genome sequencing and epidemiological data from 818 pediatric IPD isolates (1998-2016).
- Phylogenetic analysis, serotype characterization, and AMR profiling across three vaccine eras.
Main Results:
- PCV reduced vaccine serotypes but NVT expansion occurred (e.g., 22F, 33F, 15B), with regional variations.
- Serotypes 19A and 3 persisted; capsular switching led to re-emergence of pre-vaccine lineages.
- Macrolide resistance increased significantly in Calgary; penicillin resistance remained low.
Conclusions:
- Pneumococcus demonstrates sustained adaptation via serotype replacement, vaccine escape, and AMR spread.
- Genomic surveillance is vital for tracking trends and informing vaccination strategies.
Background And Aim:
Pneumococcal conjugate vaccines (PCVs) have significantly reduced pediatric invasive pneumococcal disease (IPD). However, vaccine escape variants, the emergence of non-vaccine serotypes (NVTs), and antimicrobial resistance (AMR) remain ongoing concerns. We aimed to characterize long-term trends in serotype distribution, lineage composition, and AMR patterns among pediatric IPD cases following PCV introduction in two major Canadian urban centers: Calgary, Alberta, and Toronto, Ontario.
Methods:
We combined whole-genome sequencing with epidemiologic data from 818 pediatric IPD isolates collected through population-based, active surveillance in Calgary (1998-2016) and Toronto (2009-2016). Phylogenetic analyses, serotype characterization, and AMR profiling were performed to assess temporal trends across three vaccine eras.
Results:
PCV implementation reduced vaccine type serotypes but was followed by expansion of NVTs, including serotypes 22F, 33F, and 15B, with regional differences in prevalence. Serotypes 19A and 3 persisted despite PCV13 inclusion. Several pre-vaccine-associated lineages re-emerged under NVT capsules, indicating capsular switching. Macrolide resistance increased in Calgary (7.4-29.3%), distributed across multiple lineages; penicillin resistance remained infrequent.
Conclusion:
Our findings highlight sustained pneumococcal adaptation through serotype replacement, vaccine escape, and AMR dissemination. Ongoing genomic surveillance is essential to monitor these trends and inform vaccination policies.
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