Department of Pediatrics, University of Thessaly, School of Health Sciences, Faculty of Medicine, Biopolis, Larissa, Greece.
University of Florence and Anna Meyer Children's Hospital, Florence, Italy.
Sci Rep. 2021 Dec 30;11(1):24534. doi: 10.1038/s41598-021-03720-y.
In a cross-sectional study, with the use of molecular methods, we aimed to gain insight into oropharyngeal pneumococcal colonization over time in 1212 Greek children recruited in general pediatric settings throughout the country; they were fully vaccinated with PCV13 (3 + 1 schedule). A single sample was obtained from each child at a time interval of 26 days to 70 months after administration of the 4th (booster) PCV13 dose; sampling time was divided into six time intervals. Carriage of Streptococcus pneumoniae was detected by real-time PCR targeting the lytA gene and isolates were serotyped by singleplex real-time PCR assays. Multiple control procedures to avoid false-positive results were applied. We showed an overall S. pneumoniae carriage rate of 48.6%. Serotyping identified typeable isolates in 82% of the total lytA-positive samples. Non-PCV13 serotypes represented 83.8% of total isolates when excluding serogroups with mixed PCV13 and non-PCV13 serotypes. In multivariate analysis daycare/school attendance emerged as the main contributing factor. Notably, serotypes 19A and 3 were the only two PCV13 serotypes the colonization rate of which increased over time (χ for trend P < 0.001 and P = 0.012, respectively). The application of the SP2020 gene on lytA-positive serotyped samples showed pneumococcal colonization in 97% of cases, and the overall colonization profile over time closely resembled that of the lytA gene. With the provisions of the methodological approach and age group of our study, the use of the oropharynx emerges as a reliable alternative to the nasopharynx in estimating pneumococcal carriage in epidemiological studies.
在一项横断面研究中,我们使用分子方法,旨在深入了解在希腊全国范围内的儿科常规环境中招募的 1212 名儿童在接受 PCV13(3+1 方案)完全接种后,口咽部肺炎链球菌定植随时间的变化情况;每个孩子在第 4 次(加强)PCV13 剂量后 26 天至 70 个月的时间间隔内从每个孩子中获得一个单一样本;采样时间分为六个时间间隔。通过针对 lytA 基因的实时 PCR 检测来检测肺炎链球菌的携带情况,通过单重实时 PCR 检测来对分离株进行血清型分型。应用了多种控制程序以避免假阳性结果。我们显示了 48.6%的总体肺炎链球菌携带率。血清型鉴定在总 lytA 阳性样本的 82%中鉴定出可分型的分离株。当排除包含混合 PCV13 和非 PCV13 血清型的血清群时,非 PCV13 血清型代表了总分离株的 83.8%。多变量分析显示,日托/学校出勤率是主要的促成因素。值得注意的是,血清型 19A 和 3 是仅有的两种 PCV13 血清型,其定植率随时间推移而增加(趋势 χ 值 P<0.001 和 P=0.012)。在 lytA 阳性的血清型样本上应用 SP2020 基因显示 97%的情况下存在肺炎链球菌定植,并且随着时间的推移,总体定植情况与 lytA 基因非常相似。考虑到我们研究的方法学方法和年龄组的规定,口咽部作为估计流行病学研究中肺炎链球菌携带情况的可靠替代方法出现。