Cargando…

Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV

BACKGROUND: Pneumococcal conjugate vaccines (PCVs) effectively reduce infection and asymptomatic carriage of Streptococcus pneumoniae vaccine serotypes. In 2016, Belgium replaced its infant PCV13 program by a 4-year period of PCV10. Concomitantly, S. pneumoniae serotype carriage was monitored togeth...

Descripción completa

Detalles Bibliográficos
Autores principales: Ekinci, Esra, Van Heirstraeten, Liesbet, Willen, Laura, Desmet, Stefanie, Wouters, Ine, Vermeulen, Helene, Lammens, Christine, Goossens, Herman, Van Damme, Pierre, Verhaegen, Jan, Beutels, Philippe, Theeten, Heidi, Malhotra-Kumar, Surbhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9909365/
https://www.ncbi.nlm.nih.gov/pubmed/36377804
http://dx.doi.org/10.1093/jpids/piac117
_version_ 1784884559681159168
author Ekinci, Esra
Van Heirstraeten, Liesbet
Willen, Laura
Desmet, Stefanie
Wouters, Ine
Vermeulen, Helene
Lammens, Christine
Goossens, Herman
Van Damme, Pierre
Verhaegen, Jan
Beutels, Philippe
Theeten, Heidi
Malhotra-Kumar, Surbhi
author_facet Ekinci, Esra
Van Heirstraeten, Liesbet
Willen, Laura
Desmet, Stefanie
Wouters, Ine
Vermeulen, Helene
Lammens, Christine
Goossens, Herman
Van Damme, Pierre
Verhaegen, Jan
Beutels, Philippe
Theeten, Heidi
Malhotra-Kumar, Surbhi
author_sort Ekinci, Esra
collection PubMed
description BACKGROUND: Pneumococcal conjugate vaccines (PCVs) effectively reduce infection and asymptomatic carriage of Streptococcus pneumoniae vaccine serotypes. In 2016, Belgium replaced its infant PCV13 program by a 4-year period of PCV10. Concomitantly, S. pneumoniae serotype carriage was monitored together with the carriage of other nasopharyngeal pathogens in children attending day-care centers. METHODS: From 2016 to 2019, a total of 3459 nasopharyngeal swabs were obtained from children aged 6–30 months. Culture and qPCR were used for the identification of S. pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Staphylococcus aureus and for serotyping and antimicrobial susceptibility assessment of S. pneumoniae strains. RESULTS: S. pneumoniae colonization was frequent and stable over the study years. H. influenzae and M. catarrhalis were more frequently carried (P < .001) than S. pneumoniae, by, respectively, 92.3% and 91.0% of children. Prevalence of all PCV13 serotypes together increased significantly over time from 5.8% to 19.6% (P < .001) and was attributable to the increasing prevalence of serotype 19A. Coincidently, non-vaccine serotype 6C increased (P < .001) and the overall pneumococcal non-susceptibility to tetracycline and erythromycin. Non-susceptibility to cotrimoxazole decreased (P < .001). CONCLUSIONS: The switch to a PCV program no longer covering serotypes 19A, 6A, and 3 was associated with a sustained increase of serotypes 19A and 6C in healthy children, similarly as in invasive pneumococcal disease. This resulted in a re-introduction of the 13-valent conjugate vaccine during the summer of 2019.
format Online
Article
Text
id pubmed-9909365
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-99093652023-02-09 Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV Ekinci, Esra Van Heirstraeten, Liesbet Willen, Laura Desmet, Stefanie Wouters, Ine Vermeulen, Helene Lammens, Christine Goossens, Herman Van Damme, Pierre Verhaegen, Jan Beutels, Philippe Theeten, Heidi Malhotra-Kumar, Surbhi J Pediatric Infect Dis Soc Original Articles BACKGROUND: Pneumococcal conjugate vaccines (PCVs) effectively reduce infection and asymptomatic carriage of Streptococcus pneumoniae vaccine serotypes. In 2016, Belgium replaced its infant PCV13 program by a 4-year period of PCV10. Concomitantly, S. pneumoniae serotype carriage was monitored together with the carriage of other nasopharyngeal pathogens in children attending day-care centers. METHODS: From 2016 to 2019, a total of 3459 nasopharyngeal swabs were obtained from children aged 6–30 months. Culture and qPCR were used for the identification of S. pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Staphylococcus aureus and for serotyping and antimicrobial susceptibility assessment of S. pneumoniae strains. RESULTS: S. pneumoniae colonization was frequent and stable over the study years. H. influenzae and M. catarrhalis were more frequently carried (P < .001) than S. pneumoniae, by, respectively, 92.3% and 91.0% of children. Prevalence of all PCV13 serotypes together increased significantly over time from 5.8% to 19.6% (P < .001) and was attributable to the increasing prevalence of serotype 19A. Coincidently, non-vaccine serotype 6C increased (P < .001) and the overall pneumococcal non-susceptibility to tetracycline and erythromycin. Non-susceptibility to cotrimoxazole decreased (P < .001). CONCLUSIONS: The switch to a PCV program no longer covering serotypes 19A, 6A, and 3 was associated with a sustained increase of serotypes 19A and 6C in healthy children, similarly as in invasive pneumococcal disease. This resulted in a re-introduction of the 13-valent conjugate vaccine during the summer of 2019. Oxford University Press 2022-12-20 /pmc/articles/PMC9909365/ /pubmed/36377804 http://dx.doi.org/10.1093/jpids/piac117 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of The Journal of the Pediatric Infectious Diseases Society. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Ekinci, Esra
Van Heirstraeten, Liesbet
Willen, Laura
Desmet, Stefanie
Wouters, Ine
Vermeulen, Helene
Lammens, Christine
Goossens, Herman
Van Damme, Pierre
Verhaegen, Jan
Beutels, Philippe
Theeten, Heidi
Malhotra-Kumar, Surbhi
Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV
title Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV
title_full Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV
title_fullStr Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV
title_full_unstemmed Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV
title_short Serotype 19A and 6C Account for One-Third of Pneumococcal Carriage Among Belgian Day-Care Children Four Years After a Shift to a Lower-Valent PCV
title_sort serotype 19a and 6c account for one-third of pneumococcal carriage among belgian day-care children four years after a shift to a lower-valent pcv
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9909365/
https://www.ncbi.nlm.nih.gov/pubmed/36377804
http://dx.doi.org/10.1093/jpids/piac117
work_keys_str_mv AT ekinciesra serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT vanheirstraetenliesbet serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT willenlaura serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT desmetstefanie serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT woutersine serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT vermeulenhelene serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT lammenschristine serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT goossensherman serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT vandammepierre serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT verhaegenjan serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT beutelsphilippe serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT theetenheidi serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT malhotrakumarsurbhi serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv
AT serotype19aand6caccountforonethirdofpneumococcalcarriageamongbelgiandaycarechildrenfouryearsafterashifttoalowervalentpcv