Cargando…

Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada

BACKGROUND: A few extraintestinal pathogenic Escherichia coli (ExPEC) multilocus sequence types (STs) cause the majority of community-acquired urinary tract infections (UTIs). We examine the genomic epidemiology of major ExPEC lineages, specifically factors associated with intestinal acquisition. ME...

Descripción completa

Detalles Bibliográficos
Autores principales: Fibke, Chad D, Croxen, Matthew A, Geum, Hyun Min, Glass, Magdalena, Wong, Eugenia, Avery, Brent P, Daignault, Danielle, Mulvey, Michael R, Reid-Smith, Richard J, Parmley, E Jane, Portt, Andrea, Boerlin, Patrick, Manges, Amee R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824535/
https://www.ncbi.nlm.nih.gov/pubmed/31696141
http://dx.doi.org/10.1093/ofid/ofz431
_version_ 1783464750348238848
author Fibke, Chad D
Croxen, Matthew A
Geum, Hyun Min
Glass, Magdalena
Wong, Eugenia
Avery, Brent P
Daignault, Danielle
Mulvey, Michael R
Reid-Smith, Richard J
Parmley, E Jane
Portt, Andrea
Boerlin, Patrick
Manges, Amee R
author_facet Fibke, Chad D
Croxen, Matthew A
Geum, Hyun Min
Glass, Magdalena
Wong, Eugenia
Avery, Brent P
Daignault, Danielle
Mulvey, Michael R
Reid-Smith, Richard J
Parmley, E Jane
Portt, Andrea
Boerlin, Patrick
Manges, Amee R
author_sort Fibke, Chad D
collection PubMed
description BACKGROUND: A few extraintestinal pathogenic Escherichia coli (ExPEC) multilocus sequence types (STs) cause the majority of community-acquired urinary tract infections (UTIs). We examine the genomic epidemiology of major ExPEC lineages, specifically factors associated with intestinal acquisition. METHODS: A total of 385 women with UTI caused by E. coli across Canada were asked about their diet, travel, and other exposures. Genome sequencing was used to determine both ST and genomic similarity. Logistic regression was used to identify factors associated with the acquisition of and infection with major ExPEC STs relative to minor ExPEC STs. RESULTS: ST131, ST69, ST73, ST127, and ST95 were responsible for 54% of all UTIs. Seven UTI clusters were identified, but genomes from the ST95, ST127, and ST420 clusters exhibited as few as 3 single nucleotide variations across the entire genome, suggesting recent acquisition. Furthermore, we identified a cluster of UTIs caused by 6 genetically-related ST1193 isolates carrying mutations in gyrA and parC. The acquisition of and infection with ST69, ST95, ST127, and ST131 were all associated with increased travel. The consumption of high-risk foods such as raw meat or vegetables, undercooked eggs, and seafood was associated with acquisition of and infection with ST69, ST127, and ST131, respectively. CONCLUSIONS: Reservoirs may aid in the dissemination of pandemic ExPEC lineages in the community. Identifying ExPEC reservoirs may help prevent future emergence and dissemination of high-risk lineages within the community setting.
format Online
Article
Text
id pubmed-6824535
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-68245352019-11-06 Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada Fibke, Chad D Croxen, Matthew A Geum, Hyun Min Glass, Magdalena Wong, Eugenia Avery, Brent P Daignault, Danielle Mulvey, Michael R Reid-Smith, Richard J Parmley, E Jane Portt, Andrea Boerlin, Patrick Manges, Amee R Open Forum Infect Dis Major Article BACKGROUND: A few extraintestinal pathogenic Escherichia coli (ExPEC) multilocus sequence types (STs) cause the majority of community-acquired urinary tract infections (UTIs). We examine the genomic epidemiology of major ExPEC lineages, specifically factors associated with intestinal acquisition. METHODS: A total of 385 women with UTI caused by E. coli across Canada were asked about their diet, travel, and other exposures. Genome sequencing was used to determine both ST and genomic similarity. Logistic regression was used to identify factors associated with the acquisition of and infection with major ExPEC STs relative to minor ExPEC STs. RESULTS: ST131, ST69, ST73, ST127, and ST95 were responsible for 54% of all UTIs. Seven UTI clusters were identified, but genomes from the ST95, ST127, and ST420 clusters exhibited as few as 3 single nucleotide variations across the entire genome, suggesting recent acquisition. Furthermore, we identified a cluster of UTIs caused by 6 genetically-related ST1193 isolates carrying mutations in gyrA and parC. The acquisition of and infection with ST69, ST95, ST127, and ST131 were all associated with increased travel. The consumption of high-risk foods such as raw meat or vegetables, undercooked eggs, and seafood was associated with acquisition of and infection with ST69, ST127, and ST131, respectively. CONCLUSIONS: Reservoirs may aid in the dissemination of pandemic ExPEC lineages in the community. Identifying ExPEC reservoirs may help prevent future emergence and dissemination of high-risk lineages within the community setting. Oxford University Press 2019-10-09 /pmc/articles/PMC6824535/ /pubmed/31696141 http://dx.doi.org/10.1093/ofid/ofz431 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Fibke, Chad D
Croxen, Matthew A
Geum, Hyun Min
Glass, Magdalena
Wong, Eugenia
Avery, Brent P
Daignault, Danielle
Mulvey, Michael R
Reid-Smith, Richard J
Parmley, E Jane
Portt, Andrea
Boerlin, Patrick
Manges, Amee R
Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada
title Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada
title_full Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada
title_fullStr Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada
title_full_unstemmed Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada
title_short Genomic Epidemiology of Major Extraintestinal Pathogenic Escherichia coli Lineages Causing Urinary Tract Infections in Young Women Across Canada
title_sort genomic epidemiology of major extraintestinal pathogenic escherichia coli lineages causing urinary tract infections in young women across canada
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824535/
https://www.ncbi.nlm.nih.gov/pubmed/31696141
http://dx.doi.org/10.1093/ofid/ofz431
work_keys_str_mv AT fibkechadd genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT croxenmatthewa genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT geumhyunmin genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT glassmagdalena genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT wongeugenia genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT averybrentp genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT daignaultdanielle genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT mulveymichaelr genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT reidsmithrichardj genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT parmleyejane genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT porttandrea genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT boerlinpatrick genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada
AT mangesameer genomicepidemiologyofmajorextraintestinalpathogenicescherichiacolilineagescausingurinarytractinfectionsinyoungwomenacrosscanada