# Genomic features of pneumococcal strains isolated from paediatric patients with invasive disease during pneumococcal conjugate vaccine introduction in Lima, Peru

**Authors:** Brayan E. Gonzales, David Durand, Erik H. Mercado, Marcela Lopez-Briceño, Luis González, Olguita Del Águila, Theresa J. Ochoa

PMC · DOI: 10.1099/mgen.0.001621 · Microbial Genomics · 2026-02-03

## TL;DR

This study examines how pneumococcal strains changed in Lima, Peru, after introducing vaccines, showing shifts in serotypes and increased antibiotic resistance.

## Contribution

The study provides genomic insights into pneumococcal strain evolution and antimicrobial resistance following PCV introduction in Peru.

## Key findings

- Vaccine serotypes decreased, while serotype 19A and non-vaccine serotypes increased post-PCV introduction.
- Predominant sequence types and clonal complexes shifted over time, with increased antimicrobial resistance markers.
- Whole-genome sequencing showed high concordance with phenotypic resistance testing but noted some discrepancies.

## Abstract

To determine changes in the pneumococcal serotypes, sequence types (STs), clonal complexes (CCs) and the frequency of antimicrobial resistance genes after the introduction of pneumococcal conjugate vaccines (PCVs) in Lima, Peru. Retrospective multicentre study analysing whole-genome sequencing (WGS) data from three passive surveillance studies of invasive pneumococcal disease (IPD) in paediatric patients in Lima (2006–2020). Pneumococcal typing and antimicrobial resistance were analysed using in silico genomic tools. CCs were identified with eBURST and phylogenetic results were visualized using PHYLOViZ. 262 pneumococcal isolates were analysed (104 from IPD1, 70 from IPD2 and 88 from IPD3), 55.3% from children under 2 years old, 53.1% from patients with pneumonia and 28.5% with meningitis. After the introduction of PCVs, vaccine serotypes decreased, while serotype 19A and non-vaccine serotypes increased. The predominant STs were ST156 in IPD1 (n=25) and in IPD2 (n=7); and ST320 (n=38) and ST230 (n=15) in IPD3. Sixteen CC were identified, the most frequent were CC1421 (n=58) and CC156 (n=36). The overall penicillin non-susceptibility (NS) increased from 21.8% in IPD1 to 28.6% in IPD3, ceftriaxone-NS increased from 10% to 13.1% and macrolide-NS from 24.8% to 85.7% respectively. Resistance markers for macrolides, tetracycline and cotrimoxazole increased post-PCV13. WGS predicted antimicrobial resistance with high concordance, though some discrepancies were noted with phenotypic testing methods. Important changes in the distribution of serotype and ST, especially among vaccine serotypes, have been observed. These findings highlight the importance of monitoring vaccine effectiveness and tracking changes in bacterial populations to guide future vaccine implementation.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249), meningitis (MONDO:0021108)
- **Species:** Streptococcus pneumoniae (taxon 1313)

## Full-text entities

- **Genes:** ISL1 (ISL LIM homeobox 1) [NCBI Gene 3670] {aka ISLET1, Isl-1}, SLC25A6 (solute carrier family 25 member 6) [NCBI Gene 293] {aka AAC3, ANT, ANT 2, ANT 3, ANT3, ANT3Y}, CAT (catalase) [NCBI Gene 847], CUL9 (cullin 9) [NCBI Gene 23113] {aka H7AP1, PARC}, SERPINA1 (serpin family A member 1) [NCBI Gene 5265] {aka A1A, A1AT, AAT, PI, PI1, PRO2275}
- **Diseases:** IPD2 (MESH:C564468), deaths (MESH:D003643), Disease (MESH:D004194), respiratory infection (MESH:D012141), 19A (OMIM:615528), septic arthritis (MESH:D001170), skin abscess (MESH:D000038), ovarian abscess (MESH:D010049), pneumococcal pneumonia (MESH:D011018), Pneumonia (MESH:D011014), Meningitis (MESH:D008580), otitis (MESH:D010031), bacteraemia (MESH:C531821), fasciitis (MESH:D005208), colitis (MESH:D003092), AMR (MESH:D060467), infections (MESH:D007239), GPSC (MESH:D011008), Bacterial peritonitis (MESH:D010538), sinusitis (MESH:D012852), invasive (MESH:D009361)
- **Chemicals:** penicillin (MESH:D010406), azithromycin (MESH:D017963), Macrolide (MESH:D018942), streptogramin B (MESH:D025381), beta-lactam (MESH:D047090), optoquine (MESH:C017303), ceftriaxone (MESH:D002443), fluoroquinolone (MESH:D024841), tetracycline (MESH:D013752), co-trimoxazole (MESH:D015662), Erythromycin (MESH:D004917), 7-valent pneumococcal conjugate vaccine (-), chloramphenicol (MESH:D002701), aminoglycoside (MESH:D000617)
- **Species:** Homo sapiens (human, species) [taxon 9606], Pseudogulbenkiania sp. CV10 (species) [taxon 1675542], Streptococcus pneumoniae (species) [taxon 1313]
- **Mutations:** S11F

## Full text

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## Figures

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868906/full.md

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Source: https://tomesphere.com/paper/PMC12868906