Evidence map›Paper›PMID 41842687›Full record

ArticleRisk analysis : an official publication of the Society for Risk Analysis2026

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

Tyler Stump, Carly Gomez, Jade Mitchell

Abstract read
In one paragraph

Article in Risk analysis : an official publication of the Society for Risk Analysis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Tyler StumpDepartment of Engineering Education, The Ohio State University, Ohio, Columbus, USA.
Carly GomezDepartment of Biosystems and Agricultural Engineering, Michigan State University, East Lansing, Michigan, USA.
Jade MitchellDepartment of Biosystems and Agricultural Engineering, Michigan State University, East Lansing, Michigan, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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

Indexed as

Listeria monocytogenesListeriosisStillbirthAnimalsFemaleHumansLikelihood FunctionsPregnancyRisk Assessmentdose‐responseListeria monocytogenessensitive populationstillbirth

Identifiers

PMID41842687
PMCPMC12994439

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.