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Related Experiment Video

Updated: Jun 7, 2026

EPA Method 1615. Measurement of Enterovirus and Norovirus Occurrence in Water by Culture and RT-qPCR. Part III. Virus Detection by RT-qPCR
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EPA Method 1615. Measurement of Enterovirus and Norovirus Occurrence in Water by Culture and RT-qPCR. Part III. Virus Detection by RT-qPCR

Published on: January 16, 2016

Norovirus GII.4 strain antigenic variation.

Lisa C Lindesmith1, Eric F Donaldson, Ralph S Baric

  • 1Department of Epidemiology, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA.

Journal of Virology
|October 29, 2010
PubMed
Summary

Noroviruses, a leading cause of gastroenteritis, rapidly evolve their capsid proteins. This antigenic variation helps them evade population immunity, similar to influenza, impacting vaccine development.

Area of Science:

  • Virology
  • Immunology
  • Epidemiology

Background:

  • Noroviruses are a major cause of epidemic gastroenteritis globally.
  • GII.4 norovirus strains are responsible for 80% of infections and exhibit rapid evolution.
  • Antigenic variation is hypothesized to be a key factor in GII.4 norovirus persistence.

Purpose of the Study:

  • To investigate the antigenic evolution of GII.4 norovirus major capsid proteins.
  • To test the hypothesis that antigenic variation drives GII.4 norovirus persistence against herd immunity.

Main Methods:

  • Hyperimmunization of mice with virus-like particles (VLPs) of early (1987) and contemporary (2006) GII.4 strains.
  • Characterization of monoclonal antibody (MAb) reactivity against a panel of GII.4 VLPs spanning 1987-2008.

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Published on: July 22, 2012

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  • Assessment of MAb-mediated blockade of VLP-ligand binding.
  • Main Results:

    • MAbs against the 1987 strain showed limited reactivity to VLPs post-2002.
    • MAbs against the 2006 strain recognized a broader range of VLPs but failed to recognize strains from 2007-2008.
    • Antibodies from 2006 strains primarily blocked homotypic binding, with reduced efficacy against earlier strains.

    Conclusions:

    • Direct evidence demonstrates significant antigenic evolution in GII.4 norovirus capsid proteins.
    • This variation likely serves to overcome population herd immunity, ensuring viral persistence.
    • Understanding norovirus antigenic variation is crucial for developing effective vaccines and therapeutics.