Cargando…

Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults

An experimental human challenge model with an attenuated diarrheagenic Escherichia coli (E. coli) strain has been used in food intervention studies aimed to increase resistance to E. coli infection. This study was designed to refine and expand this challenge model. In a double-blind study, healthy m...

Descripción completa

Detalles Bibliográficos
Autores principales: van Hoffen, Els, Mercenier, Annick, Vidal, Karine, Benyacoub, Jalil, Schloesser, Joyce, Kardinaal, Alwine, Lucas-van de Bos, Elly, van Alen, Ingrid, Roggero, Iris, Duintjer, Kim, Berendts, Anneke, Albers, Ruud, Kleerebezem, Michiel, ten Bruggencate, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7960709/
https://www.ncbi.nlm.nih.gov/pubmed/33723346
http://dx.doi.org/10.1038/s41598-021-85161-1
_version_ 1783665110184624128
author van Hoffen, Els
Mercenier, Annick
Vidal, Karine
Benyacoub, Jalil
Schloesser, Joyce
Kardinaal, Alwine
Lucas-van de Bos, Elly
van Alen, Ingrid
Roggero, Iris
Duintjer, Kim
Berendts, Anneke
Albers, Ruud
Kleerebezem, Michiel
ten Bruggencate, Sandra
author_facet van Hoffen, Els
Mercenier, Annick
Vidal, Karine
Benyacoub, Jalil
Schloesser, Joyce
Kardinaal, Alwine
Lucas-van de Bos, Elly
van Alen, Ingrid
Roggero, Iris
Duintjer, Kim
Berendts, Anneke
Albers, Ruud
Kleerebezem, Michiel
ten Bruggencate, Sandra
author_sort van Hoffen, Els
collection PubMed
description An experimental human challenge model with an attenuated diarrheagenic Escherichia coli (E. coli) strain has been used in food intervention studies aimed to increase resistance to E. coli infection. This study was designed to refine and expand this challenge model. In a double-blind study, healthy male subjects were orally challenged with 1E10 or 5E10 colony-forming units (CFU) of E. coli strain E1392/75-2A. Three weeks later, subjects were rechallenged with 1E10 CFU of E. coli. Before and after both challenges, clinical symptoms and infection- and immune-related biomarkers were analyzed. Subset analysis was performed on clinically high- and low-responders. Regardless of inoculation dose, the first challenge induced clinical symptoms for 2–3 days. In blood, neutrophils, CRP, CXCL10, and CFA/II-specific IgG were induced, and in feces calprotectin and CFA/II-specific IgA. Despite clinical differences between high- and low-responders, infection and immune biomarkers did not differ. The first inoculation induced protection at the second challenge, with a minor clinical response, and no change in biomarkers. The refined study design resulted in a larger dynamic range of symptoms, and identification of biomarkers induced by a challenge with the attenuated E. coli strain E1392/75-2A, which is of value for future intervention studies. Addition of a second inoculation allows to study the protective response induced by a primary infection. Clinicaltrials.gov registration: NCT02541695 (04/09/2015).
format Online
Article
Text
id pubmed-7960709
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-79607092021-03-19 Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults van Hoffen, Els Mercenier, Annick Vidal, Karine Benyacoub, Jalil Schloesser, Joyce Kardinaal, Alwine Lucas-van de Bos, Elly van Alen, Ingrid Roggero, Iris Duintjer, Kim Berendts, Anneke Albers, Ruud Kleerebezem, Michiel ten Bruggencate, Sandra Sci Rep Article An experimental human challenge model with an attenuated diarrheagenic Escherichia coli (E. coli) strain has been used in food intervention studies aimed to increase resistance to E. coli infection. This study was designed to refine and expand this challenge model. In a double-blind study, healthy male subjects were orally challenged with 1E10 or 5E10 colony-forming units (CFU) of E. coli strain E1392/75-2A. Three weeks later, subjects were rechallenged with 1E10 CFU of E. coli. Before and after both challenges, clinical symptoms and infection- and immune-related biomarkers were analyzed. Subset analysis was performed on clinically high- and low-responders. Regardless of inoculation dose, the first challenge induced clinical symptoms for 2–3 days. In blood, neutrophils, CRP, CXCL10, and CFA/II-specific IgG were induced, and in feces calprotectin and CFA/II-specific IgA. Despite clinical differences between high- and low-responders, infection and immune biomarkers did not differ. The first inoculation induced protection at the second challenge, with a minor clinical response, and no change in biomarkers. The refined study design resulted in a larger dynamic range of symptoms, and identification of biomarkers induced by a challenge with the attenuated E. coli strain E1392/75-2A, which is of value for future intervention studies. Addition of a second inoculation allows to study the protective response induced by a primary infection. Clinicaltrials.gov registration: NCT02541695 (04/09/2015). Nature Publishing Group UK 2021-03-15 /pmc/articles/PMC7960709/ /pubmed/33723346 http://dx.doi.org/10.1038/s41598-021-85161-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
van Hoffen, Els
Mercenier, Annick
Vidal, Karine
Benyacoub, Jalil
Schloesser, Joyce
Kardinaal, Alwine
Lucas-van de Bos, Elly
van Alen, Ingrid
Roggero, Iris
Duintjer, Kim
Berendts, Anneke
Albers, Ruud
Kleerebezem, Michiel
ten Bruggencate, Sandra
Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults
title Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults
title_full Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults
title_fullStr Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults
title_full_unstemmed Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults
title_short Characterization of the pathophysiological determinants of diarrheagenic Escherichia coli infection using a challenge model in healthy adults
title_sort characterization of the pathophysiological determinants of diarrheagenic escherichia coli infection using a challenge model in healthy adults
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7960709/
https://www.ncbi.nlm.nih.gov/pubmed/33723346
http://dx.doi.org/10.1038/s41598-021-85161-1
work_keys_str_mv AT vanhoffenels characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT mercenierannick characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT vidalkarine characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT benyacoubjalil characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT schloesserjoyce characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT kardinaalalwine characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT lucasvandeboselly characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT vanaleningrid characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT roggeroiris characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT duintjerkim characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT berendtsanneke characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT albersruud characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT kleerebezemmichiel characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults
AT tenbruggencatesandra characterizationofthepathophysiologicaldeterminantsofdiarrheagenicescherichiacoliinfectionusingachallengemodelinhealthyadults