Streptococcus pneumoniae serotype 3 population structure in the era of conjugate vaccines, 2001–2018

Author:

Cella Eleonora1,Sutcliffe Catherine G.2,Grant Lindsay R.2,Tso Carol2,Weatherholtz Robert C.2,Littlepage Shea2,Becenti Ladonna2,Jubair Mohammad1,Simons Brenna C.3,Harker-Jones Marcella3,Reid Raymond2,Yazzie Del4,Santosham Mathuram2,O'Brien Katherine L.2,Hammitt Laura L.2ORCID,Azarian Taj1

Affiliation:

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

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

3. Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska

4. Navajo Epidemiology Center, Window Rock, Arizona

Abstract

Background. 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. Methods. We analysed the genomic epidemiology of serotype 3 isolates collected from 129 adults and 63 children with pneumococcal carriage (n=61) or IPD (n=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. Results. The serotype 3 population structure was characterized by three dominant subpopulations: clade II (n=90, 46.9 %) and clade Iα (n=59, 30.7 %), which fall into Clonal Complex (CC) 180, and a non-CC180 clade (n=43, 22.4 %). The proportion of clade II-associated IPD cases increased significantly from 2001 to 2010 to 2011–2018 among adults (23.1–71.8 %; P<0.001) but not in children (27.3–33.3 %; P=0.84). Over the same period, the proportion of clade II-associated carriage increased; this was statistically significant among children (23.3–52.6 %; P=0.04) but not adults (0–50.0 %, P=0.08). Conclusions. In this setting with persistent serotype 3 IPD and carriage, clade II has increased since 2010. Genomic changes may be contributing to the observed trends in serotype 3 carriage and disease over time.

Funder

Robert Austrian Research Award

Publisher

Microbiology Society

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