Impact of pneumococcal conjugate vaccines on invasive pneumococcal disease-causing lineages among South African children

Invasive pneumococcal disease (IPD) due to non-vaccine serotypes after the introduction of pneumococcal conjugate vaccines (PCV) remains a global concern. This study used pathogen genomics to evaluate changes in invasive pneumococcal lineages before, during and after vaccine introduction in South Africa. We included genomes (N = 3104) of IPD isolates from individuals aged <18 years (2005-20), spanning four periods: pre-PCV, PCV7, early-PCV13, and late-PCV13. Significant incidence reductions occurred among vaccine-type lineages in the late-PCV13 period compared to the pre-PCV period. However, some vaccine-type lineages continued to cause invasive disease and showed increasing effective population size trends in the post-PCV era. A significant increase in lineage diversity was observed from the PCV7 period to the early-PCV13 period (Simpson's diversity index: 0.954, 95% confidence interval 0.948-0.961 vs 0.965, 0.962-0.969) supporting intervention-driven population structure perturbation. Increases in the prevalence of penicillin, erythromycin, and multidrug resistance were observed among non-vaccine serotypes in the late-PCV13 period compared to the pre-PCV period. In this work we highlight the importance of continued genomic surveillance to monitor disease-causing lineages post vaccination to support policy-making and future vaccine designs and considerations.

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Publication Details

Journal
Nature Communications
Published
2024-09-27
DOI
https://doi.org/10.1038/s41467-024-52459-3
Citations
15
Primary Topic
Pneumonia and Respiratory Infections
Type
article
Field-Weighted Citation Impact
5.80

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article

Impact of pneumococcal conjugate vaccines on invasive pneumococcal disease-causing lineages among South African children

Scott Hazelhurst, Jackie Kleynhans, Linda de Gouveia, Stephanie W. Lo et al.
15 citations
Nature Communications
Pneumonia and Respiratory Infections
5.80
article

Impact of pneumococcal conjugate vaccines on invasive pneumococcal disease-causing lineages among South African children

Scott Hazelhurst, Jackie Kleynhans, Linda de Gouveia, Stephanie W. Lo, Susan Meiring, Lesley McGee, Vanessa Quan, Cebile Lekhuleni, Kedibone Ndlangisa, Rebecca Ashley Gladstone, Benjamin J. Metcalf, Anne von Gottberg, Mignon du Plessis, Sopio Chochua, Sibongile Walaza, Stephen D. Bentley, Paulina A. Hawkins, Happy Skosana, Cheryl Cohen, Yuan Li, Ana D S Ferreira
article en
15 citations

Abstract

Invasive pneumococcal disease (IPD) due to non-vaccine serotypes after the introduction of pneumococcal conjugate vaccines (PCV) remains a global concern. This study used pathogen genomics to evaluate changes in invasive pneumococcal lineages before, during and after vaccine introduction in South Africa. We included genomes (N = 3104) of IPD isolates from individuals aged <18 years (2005-20), spanning four periods: pre-PCV, PCV7, early-PCV13, and late-PCV13. Significant incidence reductions occurred among vaccine-type lineages in the late-PCV13 period compared to the pre-PCV period. However, some vaccine-type lineages continued to cause invasive disease and showed increasing effective population size trends in the post-PCV era. A significant increase in lineage diversity was observed from the PCV7 period to the early-PCV13 period (Simpson's diversity index: 0.954, 95% confidence interval 0.948-0.961 vs 0.965, 0.962-0.969) supporting intervention-driven population structure perturbation. Increases in the prevalence of penicillin, erythromycin, and multidrug resistance were observed among non-vaccine serotypes in the late-PCV13 period compared to the pre-PCV period. In this work we highlight the importance of continued genomic surveillance to monitor disease-causing lineages post vaccination to support policy-making and future vaccine designs and considerations.

Nature CommunicationsVol. 15(1)
National Health Laboratory Service (ZA), Centers for Disease Control and Prevention (US), University of Cape Town (ZA), University of Oslo (NO), University of the Witwatersrand (ZA), Wellcome Sanger Institute (GB), University of Bath (GB)
Bill and Melinda Gates Foundation, Wellcome, University of Pittsburgh, Wellcome Trust, Department of Health and Social Care, National Institutes of Health, Fogarty International Center
Zero hunger
Openalex Percentile: Top 3%
Pneumonia and Respiratory Infections
5.80
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