Development of Dose‐Response Models for the Ingestion Exposure Route and Stillbirth Outcome for <i>Listeria monocytogenes</i>

Foodborne listeriosis can cause stillbirth in pregnant individuals, prompting numerous population-specific food safety guidelines. Dose-response models are employed in quantitative microbial risk assessments (QMRAs) to develop such guidelines; however, pregnant hosts are under-considered when developing dose-response models, and the few published dose-response models for pregnant hosts do not consider the biological plausibility of the model. Therefore, this study aims to develop biologically plausible dose-response models for pregnant hosts using infection and stillbirth as health outcomes. The inclusion criteria of dose-response data for this analysis required reporting of (i) quantified dose, (ii) Listeria monocytogenes as the target pathogen, (iii) infection and/or stillbirth as endpoints, and (iv) specificity to pregnant hosts. The datasets were fit individually and as pooled sets to exponential and beta-Poisson dose-response models using Maximum Likelihood Estimation (MLE). To establish uncertainty around the MLE estimates, 10,000 bootstrapped iterations were fit to the models. Recommended dose-response models for endpoints of stillbirth and infection were generated. The recommended model for infection was based on pooled guinea pig and gerbil maternal infection data fit to the beta-Poisson model, with parameters of: α = 0.0843 and N<sub>50</sub> = 1.01 × 10<sup>8</sup>. The recommended stillbirth dose-response model utilized a pooled guinea pig fetal brain infection and stillbirth dataset fit to the beta-Poisson model parameters of α = 0.575 and N<sub>50</sub> = 1.31 × 10<sup>7</sup>. Integrating such models into QMRAs for pregnant hosts supports a more health-protective assessment and decision-making process by separating sensitive populations from the general public when possible.

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Publication Details

Journal
Risk Analysis
Published
2026-03-17
DOI
https://doi.org/10.1111/risa.70204
Primary Topic
Listeria monocytogenes in Food Safety
Type
article
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article

Development of Dose‐Response Models for the Ingestion Exposure Route and Stillbirth Outcome for Listeria monocytogenes

Carly B. Gomez, Jade Mitchell, Tyler Stump
Risk Analysis
Listeria monocytogenes in Food Safety
article

Development of Dose‐Response Models for the Ingestion Exposure Route and Stillbirth Outcome for Listeria monocytogenes

Carly B. Gomez, Jade Mitchell, Tyler Stump
article en

Abstract

Foodborne listeriosis can cause stillbirth in pregnant individuals, prompting numerous population-specific food safety guidelines. Dose-response models are employed in quantitative microbial risk assessments (QMRAs) to develop such guidelines; however, pregnant hosts are under-considered when developing dose-response models, and the few published dose-response models for pregnant hosts do not consider the biological plausibility of the model. Therefore, this study aims to develop biologically plausible dose-response models for pregnant hosts using infection and stillbirth as health outcomes. The inclusion criteria of dose-response data for this analysis required reporting of (i) quantified dose, (ii) Listeria monocytogenes as the target pathogen, (iii) infection and/or stillbirth as endpoints, and (iv) specificity to pregnant hosts. The datasets were fit individually and as pooled sets to exponential and beta-Poisson dose-response models using Maximum Likelihood Estimation (MLE). To establish uncertainty around the MLE estimates, 10,000 bootstrapped iterations were fit to the models. Recommended dose-response models for endpoints of stillbirth and infection were generated. The recommended model for infection was based on pooled guinea pig and gerbil maternal infection data fit to the beta-Poisson model, with parameters of: α = 0.0843 and N<sub>50</sub> = 1.01 × 10<sup>8</sup>. The recommended stillbirth dose-response model utilized a pooled guinea pig fetal brain infection and stillbirth dataset fit to the beta-Poisson model parameters of α = 0.575 and N<sub>50</sub> = 1.31 × 10<sup>7</sup>. Integrating such models into QMRAs for pregnant hosts supports a more health-protective assessment and decision-making process by separating sensitive populations from the general public when possible.

Risk AnalysisVol. 46(4)
Ohio Department of Education (US), The Ohio State University (US), Michigan State University (US)
Zero hunger
Openalex Percentile: Top 22%
Listeria monocytogenes in Food Safety
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