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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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 |
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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 |
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