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Stability of the pneumococcal population structure in Massachusetts as PCV13 was introduced
Qiuzhi Chang1, Abbie E Stevenson2, Nicholas J Croucher3,4
1Department of Epidemiology, Harvard School of Public Health, 677 Huntington Avenue, Boston, MA, USA. qic716@mail.harvard.edu.
Insights
The 13-valent pneumococcal conjugate vaccine (PCV-13) showed initial impacts on pneumococcal serotype and sequence type (ST) frequencies in Massachusetts children in 2011. Further studies will track the long-term evolution of the pneumococcal population.
Area of Science:
- Microbiology
- Immunology
- Epidemiology
Background:
- The 7-valent pneumococcal conjugate vaccine (PCV-7) led to increased disease from non-vaccine serotypes, like 19A.
- The 13-valent pneumococcal conjugate vaccine (PCV-13) was introduced in 2010 to address these limitations.
Purpose of the Study:
- To assess the initial impact of PCV-13 introduction on the pneumococcal population in Massachusetts.
- To analyze changes in pneumococcal serotypes and sequence types (STs) following PCV-13 implementation.
Main Methods:
- Multilocus sequence typing (MLST) was used to analyze 367 pneumococcal isolates from children aged 3 months to 7 years.
- eBURST software compared pneumococcal population structure to previous years, specifically a 2009 sample.
Main Results:
- 104 distinct sequence types (STs) were identified, including 24 novel STs.
- No significant overall change in ST composition was observed compared to 2009 (p=0.39).
- Clonal dynamics were noted in serotypes 19A, 15B/C, and 6C, with expansion of ST 433 (serotype 22F) and ST 432 (serotype 21).
Conclusions:
- While overall serotype and ST composition showed little change, shifts in individual ST and serotype frequencies may be linked to PCV-13 introduction.
- This 2011 data provides a baseline for understanding the ongoing evolution of the pneumococcal population in response to PCV-13.
Background:
The success of 7-valent pneumococcal conjugate vaccination (PCV-7) introduced to the US childhood immunization schedule in 2000 was partially offset by increases in invasive pneumococcal disease (IPD) and pneumococcal carriage due to non-vaccine serotypes, in particular 19A, in the years that followed. A 13-valent conjugate vaccine (PCV-13) was introduced in 2010. As part of an ongoing study of the response of the Massachusetts pneumococcal population to conjugate vaccination, we report the findings from the samples collected in 2011, as PCV-13 was introduced.
Methods:
We used multilocus sequence typing (MLST) to analyze 367 pneumococcal isolates carried by Massachusetts children (aged 3 months-7 years) collected during the winter of 2010-11 and used eBURST software to compare the pneumococcal population structure with that found in previous years.
Results:
One hundred and four distinct sequence types (STs) were found, including 24 that had not been previously recorded. Comparison with a similar sample collected in 2009 revealed no significant overall difference in the ST composition (p = 0.39, classification index). However, we describe clonal dynamics within the important replacement serotypes 19A, 15B/C, and 6C, and clonal expansion of ST 433 and ST 432, which are respectively serotype 22F and 21 clones.
Conclusions:
While little overall change in serotypes or STs was evident, multiple changes in the frequency of individual STs and or serotypes may plausibly be ascribed to the introduction of PCV-13. This 2011 sample documents the initial impact of PCV-13 and will be important for comparison with future studies of the evolution of the pneumococcal population in Massachusetts.
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