Department of Zoology, University of Oxford, Oxford, United Kingdom ; Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
PLoS One. 2013 Nov 25;8(11):e81539. doi: 10.1371/journal.pone.0081539. eCollection 2013.
The 10-valent pneumococcal conjugate vaccine (PCV10) was introduced in Kenya in 2011. Introduction of any PCV will perturb the existing pneumococcal population structure, thus the aim was to genotype pneumococci collected in Kilifi before PCV10.
Using multilocus sequence typing (MLST), we genotyped >1100 invasive and carriage pneumococci from children, the largest collection genotyped from a single resource-poor country and reported to date. Serotype 1 was the most common serotype causing invasive disease and was rarely detected in carriage; all serotype 1 isolates were members of clonal complex (CC) 217. There were temporal fluctuations in the major circulating sequence types (STs); and although 1-3 major serotype 1, 14 or 23F STs co-circulated annually, the two major serotype 5 STs mainly circulated independently. Major STs/CCs also included isolates of serotypes 3, 12F, 18C and 19A and each shared ≤ 2 MLST alleles with STs that circulate widely elsewhere. Major CCs associated with non-PCV10 serotypes were predominantly represented by carriage isolates, although serotype 19A and 12F CCs were largely invasive and a serotype 10A CC was equally represented by invasive and carriage isolates.
Understanding the pre-PCV10 population genetic structure in Kilifi will allow for the detection of changes in prevalence of the circulating genotypes and evidence for capsular switching post-vaccine implementation.
10 价肺炎球菌结合疫苗(PCV10)于 2011 年在肯尼亚引入。任何 PCV 的引入都会改变现有的肺炎球菌种群结构,因此本研究旨在对基利菲(Kilifi)接种 PCV10 前采集的肺炎球菌进行基因分型。
我们采用多位点序列分型(MLST)方法,对 1100 余株来自儿童的侵袭性和携带性肺炎球菌进行了基因分型,这是迄今为止从单一资源匮乏国家中采集的最大肺炎球菌基因分型数据集,并进行了报道。血清型 1 是引起侵袭性疾病最常见的血清型,在携带中很少被检测到;所有血清型 1 分离株均属于克隆复合体(CC)217。主要流行序列型(ST)存在时间波动;虽然每年都会有 1-3 种主要的血清型 1、14 或 23F ST 共同流行,但两种主要的血清型 5 ST 主要独立流行。主要 ST/CC 还包括血清型 3、12F、18C 和 19A 的分离株,它们与广泛流行的其他 ST 共享的 MLST 等位基因≤2 个。与非 PCV10 血清型相关的主要 CC 主要由携带株代表,尽管血清型 19A 和 12F CC 主要是侵袭性的,而血清型 10A CC 则由侵袭性和携带性分离株同等代表。
了解基利菲接种 PCV10 前的人群遗传结构,将有助于检测流行基因型的变化,并为疫苗实施后荚膜转换提供证据。