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Pediatric urinary tract infections caused by poultry-associated Escherichia coli
Indexado
WoS WOS:001246568400001
Scopus SCOPUS_ID:85198032606
DOI 10.1128/SPECTRUM.03415-23
Año 2024
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Escherichia coli is the leading cause of urinary tract infections (UTIs) in children and adults. The gastrointestinal tract is the primary reservoir of uropathogenic E. coli, which can be acquired from a variety of environmental exposures, including retail meat. In the current study, we used a novel statistical-genomic approach to estimate the proportion of pediatric UTIs caused by foodborne zoonotic E. coli strains. E. coli urine isolates were collected from DC residents aged 2 months to 17 years from the Children's National Medical Center Laboratory, 2013-2014. During the same period, E. coli isolates were collected from retail poultry products purchased from 15 sites throughout DC. A total of 52 urine and 56 poultry isolates underwent whole-genome sequencing, core genome phylogenetic analysis, and host-origin prediction by a Bayesian latent class model that incorporated data on the presence of mobile genetic elements (MGEs) among E. coli isolates from multiple vertebrate hosts. A total of 56 multilocus sequence types were identified among the isolates. Five sequence types-ST10, ST38, ST69, ST117, and ST131-were observed among both urine and poultry isolates. Using the Bayesian latent class model, we estimated that 19% (10/52) of the clinical E. coli isolates in our population were foodborne zoonotic strains. These data suggest that a substantial portion of pediatric UTIs in the Washington DC region may be caused by E. coli strains originating in food animals and likely transmitted via contaminated poultry meat. IMPORTANCE Escherichia coli UTIs are a heavy public health burden and can have long-term negative health consequences for pediatric patients. E. coli has an extremely broad host range, including humans, chickens, turkeys, pigs, and cattle. E. coli derived from food animals is a frequent contaminant of retail meat products, but little is known about the risk these strains pose to pediatric populations. Quantifying the proportion of pediatric UTIs caused by food-animal-derived E. coli, characterizing the highest-risk strains, and identifying their primary reservoir species could inform novel intervention strategies to reduce UTI burden in this vulnerable population. Our results suggest that retail poultry meat may be an important vehicle for pediatric exposure to zoonotic E. coli strains capable of causing UTIs. Vaccinating poultry against the highest-risk strains could potentially reduce poultry colonization, poultry meat contamination, and downstream pediatric infections.

Revista



Revista ISSN
Microbiology Spectrum 2165-0497

Métricas Externas



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Disciplinas de Investigación



WOS
Microbiology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Aziz, Maliha - GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
2 Davis, Gregg S. - GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
3 Park, Daniel E. - GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
4 Idris, Azza H. - Childrens Natl Hlth Syst - Estados Unidos
NIAID - Estados Unidos
National Institute of Allergy and Infectious Diseases (NIAID) - Estados Unidos
Childrens National Health System - Estados Unidos
5 Sariya, Sanjeev - GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
6 Wang, Yashan - GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
7 Zerbonne, Sarah - GEORGE WASHINGTON UNIV - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
8 Nordstrom, Lora - Translat Genom Res Inst - Estados Unidos
Translational Genomics Research Institute - Estados Unidos
9 Weaver, Brett - Translat Genom Res Inst - Estados Unidos
Translational Genomics Research Institute - Estados Unidos
10 Statham, Sally - Translat Genom Res Inst - Estados Unidos
Translational Genomics Research Institute - Estados Unidos
11 Johnson, Timothy J. - Univ Minnesota - Estados Unidos
College of Veterinary Medicine - Estados Unidos
12 Campos, Joseph - Childrens Natl Hlth Syst - Estados Unidos
Childrens National Health System - Estados Unidos
13 Castro-Nallar, Eduardo Hombre Universidad de Talca - Chile
14 Crandall, Keith A. Hombre GEORGE WASHINGTON UNIV - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
15 Wu, Zhenke - UNIV MICHIGAN - Estados Unidos
University of Michigan School of Public Health - Estados Unidos
16 Liu, Cindy M. - GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University - Estados Unidos
Milken Institute School of Public Health - Estados Unidos
17 DeBiasi, Roberta L. - Childrens Natl Hlth Syst - Estados Unidos
GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University School of Medicine and Health Sciences - Estados Unidos
Childrens National Health System - Estados Unidos
18 Price, Lance B. - GEORGE WASHINGTON UNIV - Estados Unidos
The George Washington University - Estados Unidos
Milken Institute School of Public Health - Estados Unidos

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Financiamiento



Fuente
National Institutes of Health
Wellcome Trust
George Washington University
HHS
Wellcome Trust (WT)
George Washington University Food for Thought Pilot Award

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Agradecimientos



Agradecimiento
This work was supported by Wellcome Trust (award #201866), National Institutes of Health [grant #5R21AI117654-02 (L.B.P.), #1R01AI130066-01A1 (L.B.P.)], and the George Washington University Food for Thought Pilot Award. The funding sources had no role in the study design, data collection, analysis, interpretation, or the writing of this manuscript.
This work was supported by Wellcome Trust (award #201866), National Institutes of Health [grant #5R21AI117654-02 (L.B.P.), #1R01AI130066-01A1 (L.B.P.)], and the George Washington University Food for Thought Pilot Award. The funding sources had no role in the study design, data collection, analysis, interpretation, or the writing of this manuscript.
This work was supported by Wellcome Trust (award #201866), National Institutes of Health [grant #5R21AI117654-02 (L.B.P.), #1R01AI130066-01A1 (L.B.P.)], and the George Washington University Food for Thought Pilot Award. The funding sources had no role in the study design, data collection, analysis, interpretation, or the writing of this manuscript.

Muestra la fuente de financiamiento declarada en la publicación.