Pneumococcal carriage and disease during the implementation of PCV13: 2006 to 2016
Pneumococcal carriage and disease during the implementation of PCV13: 2006 to 2016
Streptococcus pneumoniae is both a common inhabitant of the human nasopharynx and a leading cause of morbidity and mortality. Characterisation of pneumococcal populations derived from asymptomatic carriage and invasive disease during the introduction of a 13-valent pneumococcal conjugate vaccine (PCV13) allows the impact of the vaccine to be assessed and may provide information with which to inform public health policies.
Streptococcus pneumoniae isolated from the nasopharynx of healthy children were collected alongside isolates found in invasive pneumococcal disease (IPD) from the same geographical location over a ten year period. Carriage rates and IPD incidence rates were examined to assess the impact of PCV13 on both populations. Changes to the serotype distribution in both the carriage and the disease populations were compared and a molecular investigation was performed to ascertain similarities between the populations.
Pneumococcal carriage and IPD incidence caused by PCV13 serotypes decreased following PCV13 introduction however an increase in carriage and IPD incidence caused by non-vaccine serotypes was observed. Evaluation of serotype distribution revealed that three non-vaccine serotypes had significantly higher odds of featuring in IPD; 12F, 8 and 9N. Genotypic analyses showed that while 83% of IPD isolates had the same clonal type as carriage isolates, some molecular variations within prevalent carriage isolates were not seen in the IPD population.
The increase in carriage and IPD caused by non-vaccine serotypes is compromising the benefits of PCV use. Continued surveillance is required to safeguard public health.
University of Southampton
Jones, Jessica
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March 2018
Jones, Jessica
4f58f8c6-d17e-4bdd-b78f-8f3cbabaf26a
Clarke, Stuart
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Cleary, David
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Faust, Saul
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Gladstone, Rebecca
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Jones, Jessica
(2018)
Pneumococcal carriage and disease during the implementation of PCV13: 2006 to 2016.
University of Southampton, Doctoral Thesis, 199pp.
Record type:
Thesis
(Doctoral)
Abstract
Streptococcus pneumoniae is both a common inhabitant of the human nasopharynx and a leading cause of morbidity and mortality. Characterisation of pneumococcal populations derived from asymptomatic carriage and invasive disease during the introduction of a 13-valent pneumococcal conjugate vaccine (PCV13) allows the impact of the vaccine to be assessed and may provide information with which to inform public health policies.
Streptococcus pneumoniae isolated from the nasopharynx of healthy children were collected alongside isolates found in invasive pneumococcal disease (IPD) from the same geographical location over a ten year period. Carriage rates and IPD incidence rates were examined to assess the impact of PCV13 on both populations. Changes to the serotype distribution in both the carriage and the disease populations were compared and a molecular investigation was performed to ascertain similarities between the populations.
Pneumococcal carriage and IPD incidence caused by PCV13 serotypes decreased following PCV13 introduction however an increase in carriage and IPD incidence caused by non-vaccine serotypes was observed. Evaluation of serotype distribution revealed that three non-vaccine serotypes had significantly higher odds of featuring in IPD; 12F, 8 and 9N. Genotypic analyses showed that while 83% of IPD isolates had the same clonal type as carriage isolates, some molecular variations within prevalent carriage isolates were not seen in the IPD population.
The increase in carriage and IPD caused by non-vaccine serotypes is compromising the benefits of PCV use. Continued surveillance is required to safeguard public health.
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Published date: March 2018
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Local EPrints ID: 435491
URI: http://eprints.soton.ac.uk/id/eprint/435491
PURE UUID: cf2831ec-2ac3-4ff8-96f3-857b7b1416bc
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Date deposited: 08 Nov 2019 17:30
Last modified: 17 Mar 2024 05:01
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Contributors
Author:
Jessica Jones
Thesis advisor:
Rebecca Gladstone
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