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2001-2018 年结合疫苗时代血清型 3 人群结构。

serotype 3 population structure in the era of conjugate vaccines, 2001-2018.

机构信息

Burnett School of Biomedical Sciences, University of Central Florida, Orlando, Florida.

Center for Indigenous Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

出版信息

Microb Genom. 2024 Mar;10(3). doi: 10.1099/mgen.0.001196.

Abstract

Despite use of highly effective conjugate vaccines, invasive pneumococcal disease (IPD) remains a leading cause of morbidity and mortality and disproportionately affects Indigenous populations. Although included in the 13-valent pneumococcal conjugate vaccine (PCV13), which was introduced in 2010, serotype 3 continues to cause disease among Indigenous communities in the Southwest USA. In the Navajo Nation, serotype 3 IPD incidence increased among adults (3.8/100 000 in 2001-2009 and 6.2/100 000 in 2011-2019); in children the disease persisted although the rates dropped from 5.8/100 000 to 2.3/100 000. We analysed the genomic epidemiology of serotype 3 isolates collected from 129 adults and 63 children with pneumococcal carriage (=61) or IPD (=131) from 2001 to 2018 of the Navajo Nation. Using whole-genome sequencing data, we determined clade membership and assessed changes in serotype 3 population structure over time. The serotype 3 population structure was characterized by three dominant subpopulations: (=90, 46.9 %) and (=59, 30.7 %), which fall into Clonal Complex (CC) 180, and a non-CC180 clade (=43, 22.4 %). The proportion of -associated IPD cases increased significantly from 2001 to 2010 to 2011-2018 among adults (23.1-71.8 %; <0.001) but not in children (27.3-33.3 %; =0.84). Over the same period, the proportion of associated carriage increased; this was statistically significant among children (23.3-52.6 %; =0.04) but not adults (0-50.0 %, =0.08). In this setting with persistent serotype 3 IPD and carriage, has increased since 2010. Genomic changes may be contributing to the observed trends in serotype 3 carriage and disease over time.

摘要

尽管使用了高效的结合疫苗,侵袭性肺炎球菌病(IPD)仍然是发病率和死亡率的主要原因,并且不成比例地影响着土著人群。尽管包括在 2010 年推出的 13 价肺炎球菌结合疫苗(PCV13)中,但血清型 3 仍继续在美西南地区的土著社区引起疾病。在纳瓦霍族,成人中血清型 3 IPD 发病率增加(2001-2009 年为 3.8/100000,2011-2019 年为 6.2/100000);儿童中该疾病仍然存在,尽管发病率从 5.8/100000 降至 2.3/100000。我们分析了 2001 年至 2018 年期间从纳瓦霍族的 129 名成人和 63 名携带肺炎球菌的儿童(=61 名)或 IPD(=131 名)中收集的血清型 3 分离株的基因组流行病学。使用全基因组测序数据,我们确定了谱系成员,并评估了血清型 3 人群结构随时间的变化。血清型 3 人群结构的特征是三个主要亚群:=90,46.9%)和=59,30.7%),它们属于克隆复合体(CC)180,和一个非 CC180 谱系=43,22.4%)。成人中与相关的 IPD 病例比例从 2001 年至 2010 年显著增加至 2011-2018 年(23.1-71.8%;<0.001),但在儿童中无显著变化(27.3-33.3%;=0.84)。在此期间,与相关的携带量增加;这在儿童中具有统计学意义(23.3-52.6%;=0.04),但在成人中无统计学意义(0-50.0%;=0.08)。在这种持续存在血清型 3 IPD 和携带的情况下,自 2010 年以来有所增加。基因组变化可能导致了观察到的血清型 3 携带和疾病随时间的变化趋势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c96/10963907/4c79415f8e2c/mgen-10-01196-g001.jpg

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