Next generation risk assessment: A proof of concept for the integration of genomic data on cold tolerance into quantitative microbial risk assessment for Campylobacter jejuni in poultry meat

IF 2.2 4区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
Microbial Risk Analysis Pub Date : 2026-06-01 Epub Date: 2026-01-20 DOI:10.1016/j.mran.2026.100365
Eduardo de Freitas Costa , Andries A. Kampfraath , Dirkjan Schokker , Menno van der Voort , Roan Pijnacker , Clazien J. de Vos , Eric G. Evers , Alex Bossers , Jose L. Gonzales , Ewa Pacholewicz
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Abstract

Quantitative Microbiological Risk assessment (QMRA) models are essential tools for setting up mitigation strategies. Traditional QMRA modelling approaches do not account for the correlation between genetic traits and variability among pathogens, potentially leading to over- or underestimation of microbial exposure and associated risks. We aimed to integrate genomic data into QMRA to propagate bacterial strain variability and update the existing framework of QMRA, following a Next Generation Risk Assessment (NGRA) approach. We used a benchmark QMRA model describing the prevalence and concentration of Campylobacter jejuni on chicken in all stages from farm-to-fork, to model the risk of infection and illness related to consumption of chicken meat. We integrated extended the storage step, to account for genetic variability in cold inactivation by incorporating gene-level genomic data associated with cold tolerance, derived from literature and a large C. jejuni genomic dataset, into the traditional QMRA model by setting up cold inactivation curves from existing data to map the relationship between the number of cold tolerance genes and temperature-dependent inactivation. The predicted number of cases was 8822 human cases/year in the benchmark QMRA model. The contamination of meat with C. jejuni strains having lower cold tolerance genes can reduce the expected number of human campylobacteriosis cases up to 100%; on the other hand, higher number of cold tolerance genes resulted in an increase up to 335.8% on the expected number of cases. Although our results are based on simulations, we show a potential implementation of the genetic information into QMRA, linking risk estimates with whole-genome sequencing data. More research is needed to understand how genetic features shape phenotypical characteristics, which is one of the main uncertainties in the current NGRA model, and to further explore the implications for risk management.

Abstract Image

下一代风险评估:将耐寒性基因组数据整合到禽肉中空肠弯曲杆菌的定量微生物风险评估的概念证明
定量微生物风险评估(QMRA)模型是制定缓解战略的重要工具。传统的QMRA建模方法没有考虑遗传性状和病原体变异性之间的相关性,可能导致高估或低估微生物暴露和相关风险。我们的目标是将基因组数据整合到QMRA中,以传播细菌菌株变异性并更新现有的QMRA框架,采用下一代风险评估(NGRA)方法。我们使用了一个基准QMRA模型,描述了从农场到餐桌的所有阶段鸡肉上空肠弯曲杆菌的患病率和浓度,以模拟与鸡肉消费相关的感染和疾病风险。为了解释冷失活的遗传变异性,我们整合了扩展存储步骤,通过将与耐寒性相关的基因水平基因组数据(来自文献和大型空肠C. jejuni基因组数据集)纳入传统的QMRA模型,通过从现有数据中建立冷失活曲线来绘制耐寒基因数量与温度依赖性失活之间的关系。在基准QMRA模型中,预测病例数为8822例/年。具有较低耐寒基因的空肠梭菌污染肉类可使人类弯曲杆菌病的预期病例数减少100%;另一方面,耐冷基因数量的增加导致预期病例数增加了335.8%。虽然我们的结果是基于模拟,但我们展示了将遗传信息应用于QMRA的潜在实现,将风险估计与全基因组测序数据联系起来。遗传特征是如何塑造表型特征的,这是当前NGRA模型的主要不确定性之一,需要进一步研究,并进一步探讨其对风险管理的影响。
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来源期刊
Microbial Risk Analysis
Microbial Risk Analysis Medicine-Microbiology (medical)
CiteScore
5.70
自引率
7.10%
发文量
28
审稿时长
52 days
期刊介绍: The journal Microbial Risk Analysis accepts articles dealing with the study of risk analysis applied to microbial hazards. Manuscripts should at least cover any of the components of risk assessment (risk characterization, exposure assessment, etc.), risk management and/or risk communication in any microbiology field (clinical, environmental, food, veterinary, etc.). This journal also accepts article dealing with predictive microbiology, quantitative microbial ecology, mathematical modeling, risk studies applied to microbial ecology, quantitative microbiology for epidemiological studies, statistical methods applied to microbiology, and laws and regulatory policies aimed at lessening the risk of microbial hazards. Work focusing on risk studies of viruses, parasites, microbial toxins, antimicrobial resistant organisms, genetically modified organisms (GMOs), and recombinant DNA products are also acceptable.
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