Parasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Parasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Lancet Microbe. 2022 Oct;3(10):e735-e743. doi: 10.1016/S2666-5247(22)00158-6. Epub 2022 Aug 16.
Serotype 24F is one of the emerging pneumococcal serotypes after the introduction of pneumococcal conjugate vaccine (PCV). We aimed to identify lineages driving the increase of serotype 24F in France and place these findings into a global context.
Whole-genome sequencing was performed on a collection of serotype 24F pneumococci from asymptomatic colonisation (n=229) and invasive disease (n=190) isolates among individuals younger than 18 years in France, from 2003 to 2018. To provide a global context, we included an additional collection of 24F isolates in the Global Pneumococcal Sequencing (GPS) project database for analysis. A Global Pneumococcal Sequence Cluster (GPSC) and a clonal complex (CC) were assigned to each genome. Phylogenetic, evolutionary, and spatiotemporal analysis were conducted using the same 24F collection and supplemented with a global collection of genomes belonging to the lineage of interest from the GPS project database (n=25 590).
Serotype 24F was identified in numerous countries mainly due to the clonal spread of three lineages: GPSC10 (CC230), GPSC16 (CC156), and GPSC206 (CC7701). GPSC10 was the only multidrug-resistant lineage. GPSC10 drove the increase in 24F in France and had high invasive disease potential. The international dataset of GPSC10 (n=888) revealed that this lineage expressed 16 other serotypes, with only six included in 13-valent PCV (PCV13). All serotype 24F isolates were clustered in a single clade within the GPSC10 phylogeny and long-range transmissions were detected from Europe to other continents. Spatiotemporal analysis showed GPSC10-24F took 3-5 years to spread across France and a rapid change of serotype composition from PCV13 serotype 19A to 24F during the introduction of PCV13 was observed in neighbouring country Spain.
Our work reveals that GPSC10 alone is a challenge for serotype-based vaccine strategy. More systematic investigation to identify lineages like GPSC10 will better inform and improve next-generation preventive strategies against pneumococcal diseases.
Bill & Melinda Gates Foundation, Wellcome Sanger Institute, and the US Centers for Disease Control and Prevention.
在引入肺炎球菌结合疫苗(PCV)后,血清型 24F 是新出现的肺炎球菌血清型之一。我们旨在确定推动法国血清型 24F 增加的谱系,并将这些发现置于全球背景下。
对 2003 年至 2018 年间法国 18 岁以下人群无症状定植(n=229)和侵袭性疾病(n=190)分离株中血清型 24F 肺炎球菌的全基因组测序进行分析。为了提供全球背景,我们还将 GPS 项目数据库中的 24F 分离株纳入了全球肺炎球菌测序 (GPS) 项目数据库进行分析。为每个基因组分配了一个全球肺炎球菌序列聚类 (GPSC) 和一个克隆复合体 (CC)。使用相同的 24F 集合进行系统发育、进化和时空分析,并补充来自 GPS 项目数据库中感兴趣谱系的全球基因组集合(n=25590)。
血清型 24F 在许多国家被发现,主要是由于三个谱系的克隆传播:GPSC10(CC230)、GPSC16(CC156)和 GPSC206(CC7701)。GPSC10 是唯一的多药耐药谱系。GPSC10 推动了法国 24F 的增长,并具有高侵袭性疾病的潜力。GPSC10(n=888)的国际数据集显示,该谱系表达了 16 个其他血清型,其中只有 6 个包含在 13 价 PCV(PCV13)中。所有血清型 24F 分离株都聚集在 GPSC10 系统发育的一个单一分支内,并检测到来自欧洲到其他大陆的远距离传播。时空分析表明,GPSC10-24F 花费 3-5 年时间在法国传播,在邻国西班牙,PCV13 引入期间,血清型组成从 PCV13 血清型 19A 快速转变为 24F。
我们的工作表明,GPSC10 本身就是基于血清型疫苗策略的挑战。更系统地调查像 GPSC10 这样的谱系将更好地为针对肺炎球菌疾病的下一代预防策略提供信息并加以改进。
比尔及梅琳达·盖茨基金会、桑格研究所和美国疾病控制与预防中心。