Risk of acquisition of human diarrhoeagenic Escherichia coli virulence genes in intercontinental travellers: A prospective, multi-centre study.


Journal

Travel medicine and infectious disease
ISSN: 1873-0442
Titre abrégé: Travel Med Infect Dis
Pays: Netherlands
ID NLM: 101230758

Informations de publication

Date de publication:
Historique:
received: 07 05 2018
revised: 11 12 2018
accepted: 14 12 2018
pubmed: 5 1 2019
medline: 19 2 2020
entrez: 5 1 2019
Statut: ppublish

Résumé

We studied geographic distribution of diarrhoeagenic Escherichia coli virulence genes (DEC VGs) acquisition in travellers and investigated if they acquired highly virulent EAEC/STEC hybrid strains. From the prospective, multicentre COMBAT study among 2001 Dutch travellers, 491 travellers were selected based on travel destination to 7 subregions. Faecal samples taken directly before and after travel were screened for nine DEC VGs with real-time PCR. Incidence proportions and rates were calculated for each gene and subregion. 479 travellers were analysed. 21.8% acquired aggR (EAEC), with highest acquisition rates in Northern and Western Africa and 15.3% acquired eae (STEC/EPEC) with highest rates in travellers to Western and Eastern Africa. ETEC (elt or est gene) was acquired by 4.2% of travellers and acquisition of est was associated with traveller's diarrhoea. Overall, the risk of acquiring DEC VGs was low in Southern Africa and South America. Although the combination of aggR (EAEC) and stx1/2 (STEC) was acquired by 3 travellers, these genes could not be detected together in a single E. coli strain. The risk of acquisition of DEC VGs strongly depends on the travel destination, with those travelling to Africa - except Southern Africa - having a higher risk.

Sections du résumé

BACKGROUND BACKGROUND
We studied geographic distribution of diarrhoeagenic Escherichia coli virulence genes (DEC VGs) acquisition in travellers and investigated if they acquired highly virulent EAEC/STEC hybrid strains.
METHODS METHODS
From the prospective, multicentre COMBAT study among 2001 Dutch travellers, 491 travellers were selected based on travel destination to 7 subregions. Faecal samples taken directly before and after travel were screened for nine DEC VGs with real-time PCR. Incidence proportions and rates were calculated for each gene and subregion.
RESULTS RESULTS
479 travellers were analysed. 21.8% acquired aggR (EAEC), with highest acquisition rates in Northern and Western Africa and 15.3% acquired eae (STEC/EPEC) with highest rates in travellers to Western and Eastern Africa. ETEC (elt or est gene) was acquired by 4.2% of travellers and acquisition of est was associated with traveller's diarrhoea. Overall, the risk of acquiring DEC VGs was low in Southern Africa and South America. Although the combination of aggR (EAEC) and stx1/2 (STEC) was acquired by 3 travellers, these genes could not be detected together in a single E. coli strain.
CONCLUSIONS CONCLUSIONS
The risk of acquisition of DEC VGs strongly depends on the travel destination, with those travelling to Africa - except Southern Africa - having a higher risk.

Identifiants

pubmed: 30609386
pii: S1477-8939(18)30448-4
doi: 10.1016/j.tmaid.2018.12.005
pii:
doi:

Substances chimiques

Virulence Factors 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

101362

Investigateurs

Martin C J Bootsma (MCJ)
Perry J van Genderen (PJ)
Abraham Goorhuis (A)
Martin Grobusch (M)
Nicky Molhoek (N)
Astrid M L Oude Lashof (AML)
Ellen E Stobberingh (EE)
Henri A Verbrugh (HA)

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Jarne M van Hattem (JM)

Department of Medical Microbiology, Academic Medical Center, Amsterdam, Netherlands. Electronic address: j.m.vanhattem@amc.uva.nl.

Adriana Cabal (A)

VISAVET Health Surveillance Centre, Universidad Complutense, Madrid, Spain; SaBio IREC, National Wildlife Research Institute (CSIC-UCLM-JCCM), Ciudad Real, Spain.

Maris S Arcilla (MS)

Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Centre, Rotterdam, Netherlands.

Julio Alvarez (J)

VISAVET Health Surveillance Centre, Universidad Complutense, Madrid, Spain; Departmento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense, Madrid, Spain.

Menno D de Jong (MD)

Department of Medical Microbiology, Academic Medical Center, Amsterdam, Netherlands.

Damian C Melles (DC)

Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Centre, Rotterdam, Netherlands.

John Penders (J)

Department of Medical Microbiology, Maastricht University, Maastricht, the Netherlands; School for Nutrition and Translational Research in Metabolism (NUTRIM), Care and Public Health Research Institute (Caphri), Maastricht University, Maastricht, the Netherlands.

Christian Gortázar Schmidt (CG)

SaBio IREC, National Wildlife Research Institute (CSIC-UCLM-JCCM), Ciudad Real, Spain.

Constance Schultsz (C)

Department of Medical Microbiology, Academic Medical Center, Amsterdam, Netherlands; Department of Global Health-Amsterdam-Institute for Global Health and Development, AMC, Amsterdam, the Netherlands.

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Classifications MeSH