1Infection Genomics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
2Faculty of Medicine and Institute for Life Sciences, University of Southampton, UK.
Microb Genom. 2017 Jun 9;3(6):e000119. doi: 10.1099/mgen.0.000119. eCollection 2017 Jun 30.
Serotype replacement has been reported in carriage and disease after pneumococcal conjugate vaccine (PCV) introductions in the UK and globally. We previously described concurrent expansion and decline of sequence types associated with serotype replacement over 5 years following PCV introductions in the UK. Here we use whole-genome sequencing to fully characterise the population structure of pneumococcal isolates collected over seven winters encompassing PCV7 and PCV13 introductions in the UK, investigating the importance of lineages in serotype replacement. We analysed 672 pneumococcal genomes from colonised children of 4 years old or less. The temporal prevalence of 20 lineages, defined by hierarchical Bayesian analysis of population structure (BAPS), was assessed in the context of serotype replacement. Multiple serotypes were detected in the primary winter of sampling within three vaccine-type (VT) lineages BAPS4, BAPS10 and BAPS11, in which serotype replacement were observed. In contrast, serotype replacement was not seen in the remaining three VT lineages (BAPS1, BAPS13 and BAPS14), that expressed a single serotype (6B, 6A and 3, respectively) in the primary winter. One lineage, BAPS1 serotype 6B was undetectable in the population towards the end of the study period. The dynamics of serotype replacement, in this UK population, was preceded by the presence or absence of multiple serotypes within VT lineages, in the pre-PCV population. This observation could help predict which non-vaccine types (NVTs) may be involved in replacement in future PCV introductions here and elsewhere. It could further indicate whether any antibiotic resistance associated with the lineages is likely to be affected by replacement.
血清型替换已在英国和全球范围内的肺炎球菌结合疫苗(PCV)引入后在带菌者和疾病中被报道。我们之前描述了在英国 PCV 引入后 5 年内与血清型替换相关的序列类型的同时扩张和下降。在这里,我们使用全基因组测序来充分描述在英国 PCV7 和 PCV13 引入后的七个冬季中收集的肺炎球菌分离株的群体结构,研究谱系在血清型替换中的重要性。我们分析了来自 4 岁或以下儿童的 672 个肺炎球菌基因组。在考虑血清型替换的情况下,评估了通过群体结构的分层贝叶斯分析(BAPS)定义的 20 个谱系在七个冬季中的时间流行率。在三个疫苗型(VT)谱系 BAPS4、BAPS10 和 BAPS11 中,在采样的第一个冬季中检测到了多种血清型,其中观察到了血清型替换。相比之下,在其余三个 VT 谱系(BAPS1、BAPS13 和 BAPS14)中,在第一个冬季中表达了一种单一血清型(分别为 6B、6A 和 3),没有观察到血清型替换。谱系 BAPS1 血清型 6B 在研究结束时在人群中无法检测到。在 PCV 引入之前的流行人群中,在 VT 谱系内存在或不存在多种血清型,这一现象预示着血清型替换的动态。这一观察结果可以帮助预测哪些非疫苗型(NVT)可能会在未来的 PCV 引入中参与替换,无论是在英国还是其他地方。它还可以进一步表明,与谱系相关的任何抗生素耐药性是否可能受到替换的影响。