Abstract
Background. Herd immunity is important in the effectiveness of conjugate polysaccharide vaccines against encapsulated bacteria. A large multicenter study investigated the effect of meningococcal serogroup C conjugate vaccine introduction on the meningococcal population. Methods. Carried meningococci in individuals aged 15-19 years attending education establishments were investigated before and for 2 years after vaccine introduction. Isolates were characterized by multilocus sequence typing, serogroup, and capsular region genotype and changes in phenotypes and genotypes assessed. Results. A total of 8462 meningococci were isolated from 47 765 participants (17.7%). Serogroup prevalence was similar over the 3 years, except for decreases of 80% for serogroup C and 40% for serogroup 29E. Clonal complexes were associated with particular serogroups and their relative proportions fluctuated, with 12 statistically significant changes (6 up, 6 down). The reduction of ST-11 complex serogroup C meningococci was probably due to vaccine introduction. Reasons for a decrease in serogroup 29E ST-254 meningococci (from 1.8% to 0.7%) and an increase in serogroup B ST-213 complex meningococci (from 6.7% to 10.6%) were less clear. Conclusions. Natural fluctuations in carried meningococcal genotypes and phenotypes a can be affected by the use of conjugate vaccines, and not all of these changes are anticipatable in advance of vaccine introduction.
Original language | English |
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Pages (from-to) | 1046-1053 |
Number of pages | 8 |
Journal | Journal of Infectious Diseases |
Volume | 204 |
Issue number | 7 |
DOIs | |
Publication status | Published - 1 Oct 2011 |
Bibliographical note
Funding Information:The authors are grateful to the following organizations for providing research funding: the Wellcome Trust (sampling in England and Wales); the Chief Scientist Office of the Scottish Executive Health Department (sampling in Scotland); and the Meningitis Trust (questionnaire). We thank the following for their assistance with implementation of the study: A. D. Carr, C. Lewis, D. Casey, K. T. Dunkin, C. Roberts, R. A. Barnes, J. Murray, A. Paull, Y. K. Lau (deceased), S. Welch, P. Marks, D. Turner, D. Griffiths, M. Clacher, G. Lewendon, R. Mathews, and M. E. Ramsay. We are indebted to the student volunteers and the many other individuals who made this study possible, including nurses, laboratory staff, school principals and staff, and colleagues who supported the study in various ways. Martin Maiden is a Wellcome Trust Senior Fellow in Basic Biomedical Sciences; and Derrick Crook is supported by the NIHR Biomedical Research Centre, Oxford.
Funding Information:
This work was supported by the Wellcome Trust (062057).