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Published on: September 11, 2020
Trends in serotypes and sequence types among cases of invasive pneumococcal disease in Scotland, 1999-2010
Karen E Lamb1, Stefan Flasche2, Mathew Diggle3
1Department of Mathematics and Statistics, University of Strathclyde, 26 Richmond Street, Glasgow, United Kingdom; Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Royal Children's Hospital, Flemington Road, Parkville, VIC, Australia.
Insights
The 7-valent pneumococcal conjugate vaccine (PCV7) significantly reduced invasive pneumococcal disease (IPD) in Scotland, especially in children under 5. Post-vaccination changes in serotypes were linked to pre-existing serotype-ST associations.
Area of Science:
- Microbiology
- Epidemiology
- Vaccinology
Background:
- The 7-valent pneumococcal conjugate vaccine (PCV7) was integrated into the UK's routine childhood immunization program in 2006.
- Invasive pneumococcal disease (IPD) surveillance in Scotland provides data on serotype and sequence type (ST) distribution.
Purpose of the Study:
- To analyze trends in pneumococcal serotypes and multi-locus sequence types (STs) in Scotland before and after PCV7 introduction.
- To evaluate the impact of PCV7 on IPD incidence across different age groups.
Main Methods:
- Utilized data from the Scottish Invasive Pneumococcal Disease Enhanced Surveillance system (1999-2010).
- Employed logistic and Poisson regression modeling to assess temporal trends.
- Analyzed isolates from blood and cerebrospinal fluid.
Main Results:
- PCV7 introduction led to a 69% reduction in IPD among children under 5 and a 57% reduction in those aged 5-64.
- No significant change in IPD incidence was observed in individuals aged 65 and over, with an increase in non-PCV7 serotypes.
- Post-PCV7 prevalent serotypes were associated with STs linked to the original PCV7 serotypes.
Conclusions:
- Serotype and ST surveillance in Scotland revealed a relationship between capsule types and bacterial clones post-vaccination.
- Observed serotype distribution changes are influenced by pre-existing serotype-ST associations.
- Findings inform predictions for replacement serotypes and the impact of higher-valency vaccines.
Introduction:
The 7-valent pneumococcal conjugate vaccine (Prevenar(®), Wyeth; PCV7) was introduced to the UK paediatric immunisation schedule in 2006. This study investigates trends in serotypes and multi locus sequence types (STs) among cases of invasive pneumococcal disease (IPD) in Scotland prior to, and following, the introduction of PCV7.
Methods:
Scottish Invasive Pneumococcal Disease Enhanced Surveillance has records of all cases of IPD in Scotland since 1999. Cases diagnosed from blood or cerebrospinal fluid isolates until 2010 were analysed. Logistic and poisson regression modelling was used to assess trends prior to and following the introduction of PCV7.
Results:
Prior to PCV7 use, on average 650 cases of IPD were reported each year; 12% occurred in those aged <5 years and 35% affected those aged over 65 years. Serotypes in PCV7 represented 47% of cases (68% in <5 year olds). The serotype and ST distribution was relatively stable with only serotype 1 and associated ST 306 showing an increasing trend. PCV7 introduction was associated with a 69% (95% CI: 50%, 80%) reduction in the incidence of IPD among those aged <5 years, a 57% (95% CI: 47%, 66%) reduction among those aged 5-64 years but no significant change among those aged 65 years and over where increases in non-PCV7 serotypes were observed. Serotypes which became more prevalent post-PCV7 are those which were associated with STs related to the PCV7 serotypes.
Conclusions:
Routine serotyping and sequence typing in Scotland allowed the assessment of the relationship between the capsule and the clones in the post vaccination era. Changes in the distribution of serotypes post PCV7 introduction appear to be driven by associations between serotypes and STs prior to PCV7 introduction. This has implications for the possible effects of the introduction of higher valency vaccines and could aid in predicting replacement serotypes in IPD.
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