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Serotype distribution and antimicrobial resistance in pediatric invasive pneumococcal pneumonia: A Laboratory
Jonathan Zintgraff1, Paula Gagetti2, Nahuel Sánchez Eluchans1
1Servicio Bacteriología Clínica, Departamento de Bacteriología, Instituto Nacional de Enfermedades Infecciosas (INEI)-ANLIS "Dr. Carlos G. Malbrán", Buenos Aires, Argentina.
Insights
Invasive pneumococcal pneumonia (IPP) in Argentine children shows shifts in serotypes post-vaccination, with concerning multidrug resistance in key strains. Enhanced surveillance and broader vaccine coverage are crucial.
Area of Science:
- Microbiology
- Epidemiology
- Public Health
Background:
- Streptococcus pneumoniae is a major cause of child mortality globally.
- Vaccine introductions alter pneumococcal serotype distribution.
- This study examines invasive pneumococcal pneumonia (IPP) in Argentine children (2022-2024).
Purpose of the Study:
- To characterize the contemporary epidemiology of IPP in Argentine children.
- To identify shifts in serotype distribution following vaccine implementation.
- To assess antimicrobial resistance patterns in invasive pneumococcal isolates.
Main Methods:
- Analysis of 316 invasive pneumonia isolates from 78 pediatric hospitals across Argentina.
- Serotyping using the Quellung reaction.
- Antimicrobial susceptibility testing via CLSI agar dilution.
Main Results:
- Serotypes 3, 19A, and 14 remain dominant; non-vaccine type 12F is emerging.
- Age-specific patterns observed, with unique serotypes in infants and older children.
- High susceptibility to beta-lactams, but 24.3% multidrug resistance noted, especially in serotypes 19A and 24F/A/B.
Conclusions:
- Significant shifts in pneumococcal serotype epidemiology post-PCV13 implementation.
- Persistent vaccine-type circulation and emergence of non-vaccine types necessitate ongoing surveillance.
- Need for next-generation vaccines with broader coverage and enhanced surveillance systems to monitor serotype replacement.
Background:
Streptococcus pneumoniae remains a leading global cause of pediatric morbidity and mortality, with evolving serotype distributions following vaccine introductions. This national surveillance study characterizes the contemporary epidemiology of invasive pneumococcal pneumonia (IPP) among Argentine children under 11 years (2022-2024).
Methods:
We analyzed 316 invasive pneumonia isolates from 78 pediatric hospitals across 24 jurisdictions, obtained through Argentina's National IPD Surveillance System. Serotyping (Quellung reaction) and antimicrobial susceptibility testing (CLSI agar dilution) were performed. Isolates were stratified by age (<2, 2-5, 6-10 years) and clinical presentation.
Results:
The surveillance showed persistent dominance of vaccine-type serotypes 3 (22.1 %), 19A (12.0 %), and 14 (6.3 %), alongside emerging non-vaccine type 12F (6.7 %). Distinct age-specific patterns emerged, with serotypes 7F and 1 predominating in 6-10 years and 24A exclusively detected in infants. Serotypes 3 and 19A demonstrated a significant association with pleural effusion, while serotype 24B was the dominant variant in non-effusion invasive pneumonia cases. Antimicrobial susceptibility testing revealed high susceptibility to β-lactams, with 94 % of isolates susceptible to penicillin and amoxicillin. However, a concerning 24.3 % rate of multidrug resistance was observed, primarily concentrated in serotypes 19A and 24F/A/B.
Conclusions:
Our analysis breaks significant shifts in pneumococcal serotype epidemiology following PCV13 implementation, with three key patterns emerging: (1) persistent circulation of vaccine-type serotypes 3 and 19A, (2) emergence of non-vaccine type particularly 12F and 24B, and (3) dynamic fluctuations in serotype distribution suggesting ongoing selective pressure. These evolving epidemiological patterns, coupled with concerning multidrug resistance in key serotypes 19A and 24F/A/B, underscore two critical needs: enhanced national surveillance systems to monitor serotype replacement, and the evaluation of next-generation vaccines that provide broader coverage against both persistent vaccine-types and emerging non-vaccine types.
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