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多种诺如病毒剂量反应模型预测风险的比较及其对定量微生物风险评估的意义。

Comparison of Risk Predicted by Multiple Norovirus Dose-Response Models and Implications for Quantitative Microbial Risk Assessment.

机构信息

Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA, USA.

Soller Environmental, Berkeley, Inc., Berkeley, CA, USA.

出版信息

Risk Anal. 2017 Feb;37(2):245-264. doi: 10.1111/risa.12616. Epub 2016 Jun 10.

Abstract

The application of quantitative microbial risk assessments (QMRAs) to understand and mitigate risks associated with norovirus is increasingly common as there is a high frequency of outbreaks worldwide. A key component of QMRA is the dose-response analysis, which is the mathematical characterization of the association between dose and outcome. For Norovirus, multiple dose-response models are available that assume either a disaggregated or an aggregated intake dose. This work reviewed the dose-response models currently used in QMRA, and compared predicted risks from waterborne exposures (recreational and drinking) using all available dose-response models. The results found that the majority of published QMRAs of norovirus use the F hypergeometric dose-response model with α = 0.04, β = 0.055. This dose-response model predicted relatively high risk estimates compared to other dose-response models for doses in the range of 1-1,000 genomic equivalent copies. The difference in predicted risk among dose-response models was largest for small doses, which has implications for drinking water QMRAs where the concentration of norovirus is low. Based on the review, a set of best practices was proposed to encourage the careful consideration and reporting of important assumptions in the selection and use of dose-response models in QMRA of norovirus. Finally, in the absence of one best norovirus dose-response model, multiple models should be used to provide a range of predicted outcomes for probability of infection.

摘要

定量微生物风险评估(QMRAs)在理解和减轻诺如病毒相关风险方面的应用越来越普遍,因为全球范围内爆发的频率很高。QMRAs 的一个关键组成部分是剂量反应分析,这是剂量与结果之间关联的数学特征。对于诺如病毒,有多种剂量反应模型,这些模型假设摄入剂量是离散的或聚合的。本研究综述了目前在 QMRA 中使用的剂量反应模型,并比较了使用所有可用剂量反应模型的饮用水(娱乐和饮用)暴露的预测风险。结果发现,大多数已发表的诺如病毒 QMRAs 使用 F 超几何剂量反应模型,α = 0.04,β = 0.055。与其他剂量反应模型相比,该剂量反应模型对 1-1000 个基因组当量拷贝范围内的剂量预测出相对较高的风险估计。剂量反应模型之间预测风险的差异在小剂量时最大,这对饮用水 QMRAs 中诺如病毒浓度较低的情况有影响。基于综述,提出了一套最佳实践,以鼓励在诺如病毒 QMRA 中仔细考虑和报告选择和使用剂量反应模型时的重要假设。最后,在没有最佳诺如病毒剂量反应模型的情况下,应使用多种模型提供感染概率的预测结果范围。

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