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Frontiers in Microbiology

dc.contributor.authorThystrup, Cecilie
dc.contributor.authorBrinch, Maja Lykke
dc.contributor.authorHenri, Clementine
dc.contributor.authorMughini-Gras, Lapo
dc.contributor.authorFranz, Eelco
dc.contributor.authorWieczorek, Kinga
dc.contributor.authorGutierrez, Montserrat
dc.contributor.authorPrendergast, Deirdre M.
dc.contributor.authorDuffy, Geraldine
dc.contributor.authorBurgess, Catherine M.
dc.contributor.authorBolton, Declan
dc.contributor.authorAlvarez, Julio
dc.contributor.authorLopez-Chavarrias, Vicente
dc.contributor.authorRosendal, Thomas
dc.contributor.authorClemente, Lurdes
dc.contributor.authorAmaro, Ana
dc.contributor.authorZomer, Aldert L.
dc.contributor.authorGrimstrup, Joensen Katrine
dc.contributor.authorMøller, Nielsen Eva
dc.contributor.authorScavia, Gaia
dc.contributor.authorSkarżyńska, Magdalena
dc.contributor.authorPinto, Miguel
dc.contributor.authorOleastro, Mónica
dc.contributor.authorCha, Wonhee
dc.contributor.authorThépault, Amandine
dc.contributor.authorRivoal, Katell
dc.contributor.authorDenis, Martine
dc.contributor.authorChemaly, Marianne
dc.contributor.authorHald, Tine
dc.date.accessioned2025-02-19T10:24:26Z
dc.date.available2025-02-19T10:24:26Z
dc.date.issued2025
dc.identifierhttps://dspace.piwet.pulawy.pl/xmlui/handle/123456789/787
dc.identifier.issn1664-302X
dc.identifier.urihttps://www.frontiersin.org/articles/10.3389/fmicb.2025.1519189
dc.description.abstractIntroduction: Infections caused by Campylobacter spp. represent a severe threat to public health worldwide. National action plans have included source attribution studies as a way to quantify the contribution of specific sources and understand the dynamic of transmission of foodborne pathogens like Salmonella and Campylobacter. Such information is crucial for implementing targeted intervention. The aim of this study was to predict the sources of humancampylobacteriosis cases across multiple countries using available whole-genome sequencing (WGS) data and explore the impact of data availability andsample size distribution in a multi-country source attribution model.Methods: We constructed a machine-learning model using k-mer frequency patterns as input data to predict human campylobacteriosis cases per source.We then constructed a multi-country model based on data from all countries.Results using different sampling strategies were compared to assess the impact of unbalanced datasets on the prediction of the cases.Results: The results showed that the variety of sources sampled and the quantity of samples from each source impacted the performance of the model. Most cases were attributed to broilers or cattle for the individual and multi-country models. The proportion of cases that could be attributed with 70% probability to a source decreased when using the down-sampled data set (535 vs. 273 of 2627 cases). The baseline model showed a higher sensitivity compared to the down-sampled model, where samples per source were more evenly distributed. The proportion of cases attributed to non-domestic source was higher but varied depending on the sampling strategy. Both models showed that most cases could be attributed to domestic sources in each country (baseline: 248/273 cases, 91%; down-sampled: 361/535 cases, 67%;).Discussion: The sample sizes per source and the variety of sources included in the model influence the accuracy of the model and consequently theuncertainty of the predicted estimates. The attribution estimates for sources with a high number of samples available tend to be overestimated, whereasthe estimates for source with only a few samples tend to be underestimated.Reccomendations for future sampling strategies include to aim for a more balanced sample distribution to improve the overall accuracy and utility of source attribution efforts.
dc.language.isoEN
dc.publisherFRONTIERS MEDIA SA
dc.subjectsource attribution
dc.subjectfoodborne disease
dc.subjectcampylobacteriosis
dc.subjectmachine learning
dc.subjectEuropean union
dc.titleSource attribution of human Campylobacter infection: a multi-country model in the European Union.
dcterms.bibliographicCitation2025 vol. 16
dcterms.titleFrontiers in Microbiology
dc.identifier.doihttps://doi.org/10.3389/fmicb.2025.1519189


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