Chang Qiuzhi, Stevenson Abbie E, Croucher Nicholas J, Lee Grace M, Pelton Stephen I, Lipsitch Marc, Finkelstein Jonathan A, Hanage William P
Department of Epidemiology, Harvard School of Public Health, 677 Huntington Avenue, Boston, MA, USA.
Department of Infectious Disease Epidemiology, Imperial College London, London, W2 1PG, UK.
BMC Infect Dis. 2015 Feb 18;15:68. doi: 10.1186/s12879-015-0797-z.
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.
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.
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.
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.
2000年引入美国儿童免疫计划的7价肺炎球菌结合疫苗(PCV-7)的成效,在随后几年中因非疫苗血清型(特别是19A)导致的侵袭性肺炎球菌疾病(IPD)和肺炎球菌携带率增加而部分抵消。2010年引入了13价结合疫苗(PCV-13)。作为对马萨诸塞州肺炎球菌群体对结合疫苗反应的一项正在进行的研究的一部分,我们报告了在引入PCV-13的2011年所采集样本的研究结果。
我们使用多位点序列分型(MLST)分析了2010 - 11年冬季采集的马萨诸塞州儿童(3个月至7岁)携带的367株肺炎球菌分离株,并使用eBURST软件将肺炎球菌群体结构与前几年的结构进行比较。
共发现104种不同的序列类型(STs),其中24种此前未被记录。与2009年采集的类似样本相比,ST组成没有显著的总体差异(p = 0.39,分类指数)。然而,我们描述了重要替代血清型19A、15B/C和6C内的克隆动态,以及分别为血清型22F和21克隆的ST 433和ST 432的克隆扩张。
虽然血清型或STs总体变化不大,但个别STs和/或血清型频率的多种变化可能合理地归因于PCV-13的引入。这个2011年的样本记录了PCV-13的初步影响,对于与马萨诸塞州肺炎球菌群体演变的未来研究进行比较将很重要。