Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne Pathogens

Different techniques are available for assessing differences in virulence of bacterial foodborne pathogens. The use of animal models or human volunteers is not expedient for various reasons; the use of epidemiological data is often hampered by lack of crucial data. In this paper, we describe a stati...

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Main Authors: Lucas M. Wijnands, Peter F. M. Teunis, Angelina F. A. Kuijpers, Ellen H. M. Delfgou-Van Asch, Annemarie Pielaat
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-06-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmicb.2017.01139/full
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author Lucas M. Wijnands
Peter F. M. Teunis
Peter F. M. Teunis
Angelina F. A. Kuijpers
Ellen H. M. Delfgou-Van Asch
Annemarie Pielaat
author_facet Lucas M. Wijnands
Peter F. M. Teunis
Peter F. M. Teunis
Angelina F. A. Kuijpers
Ellen H. M. Delfgou-Van Asch
Annemarie Pielaat
author_sort Lucas M. Wijnands
collection DOAJ
description Different techniques are available for assessing differences in virulence of bacterial foodborne pathogens. The use of animal models or human volunteers is not expedient for various reasons; the use of epidemiological data is often hampered by lack of crucial data. In this paper, we describe a static, sequential gastrointestinal tract (GIT) model system in which foodborne pathogens are exposed to simulated gastric and intestinal contents of the human digestive tract, including the interaction of pathogens with the intestinal epithelium. The system can be employed with any foodborne bacterial pathogens. Five strains of Salmonella Heidelberg and one strain of Salmonella Typhimurium were used to assess the robustness of the system. Four S. Heidelberg strains originated from an outbreak, the fifth S. Heidelberg strain and the S. Typhimurium strain originated from routine meat inspections. Data from plate counts, collected for determining the numbers of surviving bacteria in each stage, were used to quantify both the experimental uncertainty and biological variability of pathogen survival throughout the system. For this, a hierarchical Bayesian framework using Markov chain Monte Carlo (MCMC) was employed. The model system is able to distinguish serovars/strains for in vitro infectivity when accounting for within strain biological variability and experimental uncertainty.
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spelling doaj.art-4e5570a8af5a4654a0b8887ff493f7172022-12-22T02:08:14ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2017-06-01810.3389/fmicb.2017.01139264776Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne PathogensLucas M. Wijnands0Peter F. M. Teunis1Peter F. M. Teunis2Angelina F. A. Kuijpers3Ellen H. M. Delfgou-Van Asch4Annemarie Pielaat5National Institute of Public Health and the EnvironmentBilthoven, NetherlandsNational Institute of Public Health and the EnvironmentBilthoven, NetherlandsRollins School of Public Health, Emory UniversityAtlanta, GA, United StatesNational Institute of Public Health and the EnvironmentBilthoven, NetherlandsNational Institute of Public Health and the EnvironmentBilthoven, NetherlandsNational Institute of Public Health and the EnvironmentBilthoven, NetherlandsDifferent techniques are available for assessing differences in virulence of bacterial foodborne pathogens. The use of animal models or human volunteers is not expedient for various reasons; the use of epidemiological data is often hampered by lack of crucial data. In this paper, we describe a static, sequential gastrointestinal tract (GIT) model system in which foodborne pathogens are exposed to simulated gastric and intestinal contents of the human digestive tract, including the interaction of pathogens with the intestinal epithelium. The system can be employed with any foodborne bacterial pathogens. Five strains of Salmonella Heidelberg and one strain of Salmonella Typhimurium were used to assess the robustness of the system. Four S. Heidelberg strains originated from an outbreak, the fifth S. Heidelberg strain and the S. Typhimurium strain originated from routine meat inspections. Data from plate counts, collected for determining the numbers of surviving bacteria in each stage, were used to quantify both the experimental uncertainty and biological variability of pathogen survival throughout the system. For this, a hierarchical Bayesian framework using Markov chain Monte Carlo (MCMC) was employed. The model system is able to distinguish serovars/strains for in vitro infectivity when accounting for within strain biological variability and experimental uncertainty.http://journal.frontiersin.org/article/10.3389/fmicb.2017.01139/fullmodel-systemGI-tractinfectionfoodborne pathogensBayesianquantification
spellingShingle Lucas M. Wijnands
Peter F. M. Teunis
Peter F. M. Teunis
Angelina F. A. Kuijpers
Ellen H. M. Delfgou-Van Asch
Annemarie Pielaat
Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne Pathogens
Frontiers in Microbiology
model-system
GI-tract
infection
foodborne pathogens
Bayesian
quantification
title Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne Pathogens
title_full Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne Pathogens
title_fullStr Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne Pathogens
title_full_unstemmed Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne Pathogens
title_short Quantification of Salmonella Survival and Infection in an In vitro Model of the Human Intestinal Tract as Proxy for Foodborne Pathogens
title_sort quantification of salmonella survival and infection in an in vitro model of the human intestinal tract as proxy for foodborne pathogens
topic model-system
GI-tract
infection
foodborne pathogens
Bayesian
quantification
url http://journal.frontiersin.org/article/10.3389/fmicb.2017.01139/full
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