Nasal carriage of Streptococcus pneumoniae serotypes and Staphylococcus aureus in Streptococcus pneumoniae-vaccinated and non-vaccinated young children
Related Experiment Video
Updated: May 21, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
N H T M Dukers-Muijrers1, E Stobberingh2, P Beisser2
1Department of Sexual Health, Infectious Diseases and Environmental Health, South Limburg Public Health Service, Geleen, The Netherlands.
Insights
Streptococcus pneumoniae (SPn) conjugate vaccination (PCV) increased non-vaccine type SPn carriage. Staphylococcus aureus (SA) carriage was inversely associated with vaccine-type SPn carriage, particularly with SPn serotype 19A.
Area of Science:
- Pediatrics
- Infectious Diseases
- Vaccinology
Background:
- Streptococcus pneumoniae (SPn) conjugate vaccination (PCV) has shifted invasive pneumococcal disease (IPD) to non-vaccine types.
- An increased burden of Staphylococcus aureus (SA) following PCV implementation has been suggested.
Purpose of the Study:
- To assess the epidemiology of SA and SPn nasal carriage in children attending day-care centers.
- To investigate the association between PCV dosage and SPn/SA carriage.
Main Methods:
- Cross-sectional study of 620 children at day-care centers.
- Analysis of SPn and SA nasal carriage, with 141 children having received 1-4 doses of PCV7.
Main Results:
- Higher PCV7 dosage correlated with non-vaccine type SPn carriage.
- SA carriage was inversely associated with vaccine-type SPn carriage.
- SPn serotype 19A exhibited higher SA co-carriage rates.
Conclusions:
- PCV7 implementation did not prevent children from participating in SPn transmission chains.
- Findings inform monitoring of SA and SPn diseases and the vaccination policy debate regarding PCV7 to PCV10 transition.
Abstract:
Since the implementation of Streptococcus pneumoniae (SPn) conjugate vaccination (PCV), non-vaccine types have prevailed in invasive pneumococcal disease (IPD), and an increase in Staphylococcus aureus (SA) burden has been suggested. Here, we assess the epidemiology of SA and SPn nasal carriage in 620 children at day-care centres; 141 of these children had received 1-4 PCV7 doses. A higher vaccine dosage was associated with non-vaccine-type SPn carriage. Of all SPn isolates, 45% were PCV7 types, 1% were additional PCV10 types and 22% were the three additional PCV13 types. SA carriage was inversely associated with vaccine-type SPn carriage. SPn serotype 19A showed higher SA co-carriage rates compared to other SPn serotypes. PCV7 implementation does not prevent children from being part of the IPD-related SPn transmission chain. These results contribute to the monitoring of SA- and SPn-related disease and add to the debate on the current national vaccination policy that recently included a change from PCV7 to PCV10.
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