Related Experiment Video
Updated: Aug 6, 2026

EPA Method 1615. Measurement of Enterovirus and Norovirus Occurrence in Water by Culture and RT-qPCR. I. Collection of Virus Samples
Published on: March 28, 2015
Revisiting norovirus dose-response models: a meta-analysis and multi-model comparison for waterborne risk assessment
Zejun Liu1, Masaaki Kitajima2, Hiroyuki Katayama3
1Department of Urban Engineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.
None:
Norovirus is a leading cause of gastroenteritis worldwide, and robust dose-response models are essential for quantitative microbial risk assessment (QMRA). However, existing models are constrained by limited human challenge data and a lack of systematic multi-model comparison, particularly for GII norovirus. In this study, we conducted a meta-analysis of 408 publications and extracted 37 dose-response datasets. Five models, including three models incorporating an immunity parameter, were fitted separately to GI and GII data using maximum likelihood estimation. Apparent and consistent immunity was observed for GI (φ = 0.31-0.32), whereas susceptibility/immunity-related signals were weak for GII and model-dependent (φ = 0-0.02 in most models). The estimated one particle infection probability (Pinf(1)) varied substantially across models (0.08%-45.61%), highlighting strong structural uncertainty, particularly in the low-dose range where observed data are limited. Aggregation-related parameters were highly model-dependent, suggesting that aggregation functions as an effective fitting parameter rather than a directly measured property. The conditional illness probability was best represented by a one-inflated beta distribution for both GI and GII, with GII showing a stronger concentration near 1. Scenario-based QMRA across four exposure pathways showed that log reduction values (LRVs) to achieve acceptable safety level varied considerably across models (differences >2 log10), and followed the scenario order: drinking > toothbrushing > showering > swimming. Overall, these findings demonstrate that norovirus risk estimates are highly sensitive to model structure and assumptions, underscoring the need to explicitly consider structural uncertainty in waterborne QMRA.
Related Concept Videos
Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions
Pharmacodynamic Models: Direct Effect Model and Indirect Response Model
Pharmacokinetic Models: Comparison and Selection Criterion
Physiological models take a detailed approach by considering specific molecular processes. They can predict drug distribution, metabolism, and elimination changes, providing a comprehensive understanding of how drugs interact with the body.
Bioavailability Study Design: Single Versus Multiple Dose Studies
Pharmacodynamic Models: Additive and Proportional Drug Effect Model
Determination of Multiple Dosing Parameters: Loading and Maintenance Doses

