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Updated: Jun 17, 2026

Alternative In Vitro Methods for the Determination of Viral Capsid Structural Integrity
Published on: November 16, 2017
Mechanism of inactivation of murine norovirus-1 by high pressure processing
Qingjuan Tang1, Dan Li, Jie Xu
1College of Food Science and Engineering, Ocean University of China, No 5, Yushan Road, Qingdao, Shandong Province 266003, PR China.
Abstract:
Murine norovirus-1 (MNV) is currently the most suitable surrogate for human norovirus. The mechanism of MNV-1 inactivation by high pressure processing (HPP) was investigated. HPP-treated MNV could not bind to its target receptor and therefore could not initiate infection of mouse RAW cells. The integrity of the capsid was not affect by HPP. Partial motif changes of the viral capsid caused by HPP were accessed by induced sensitivity to proteinase K.
Insights
High pressure processing (HPP) inactivates murine norovirus-1 (MNV) by preventing viral binding to host cells, not by damaging the capsid. This mechanism offers insights into norovirus inactivation strategies.
Area of Science:
- Virology
- Food Science
- Microbiology
Background:
- Murine norovirus-1 (MNV) serves as a key surrogate for studying human norovirus.
- Understanding norovirus inactivation mechanisms is crucial for food safety and public health.
Purpose of the Study:
- To investigate the mechanism by which high pressure processing (HPP) inactivates MNV-1.
- To determine if HPP affects viral capsid integrity or receptor binding.
Main Methods:
- MNV-1 was subjected to high pressure processing (HPP).
- The ability of HPP-treated MNV-1 to bind to its target receptor was assessed.
- Viral capsid integrity was evaluated, including sensitivity to proteinase K digestion.
Main Results:
- HPP-treated MNV-1 lost its ability to bind to the target receptor.
- The overall integrity of the viral capsid remained unaffected by HPP.
- Partial motif changes in the viral capsid were detected, indicated by increased sensitivity to proteinase K.
Conclusions:
- HPP inactivates MNV-1 by disrupting its receptor-binding capability, not by compromising capsid structure.
- The findings suggest that HPP is a viable method for norovirus inactivation, preserving capsid integrity while blocking infectivity.
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