Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera.

Front Microbiol

Guangdong Provincial Key Laboratory of Tropical Disease Research, Department of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, China.

Published: December 2020

AI Article Synopsis

  • The study focused on characterizing the diversity and antigenic relatedness of various norovirus GI genotypes, particularly during a gastroenteritis outbreak linked to the GI.3 strain.
  • The research compared the phylogenetic relationships, HBGA binding profiles, and immune responses of GI.2, GI.3, and GI.9 strains using mouse and patient serums.
  • Results showed a weak immune response against GI.3 in the general population, contributing to the outbreak, while also revealing potential insights for optimizing norovirus vaccine design based on immunotype groupings.

Article Abstract

Characterizing diversity and the antigenic relatedness of norovirus remains a primary focus in understanding its biological properties and vaccine designs. The precise antigenic and serological features of GI genotypes have not been studied. The study represented an investigation on a gastroenteritis outbreak related to GI.3 norovirus and the three most detected GI genotypes, GI.2 (belonging to immunotype B), GI.3 and GI.9 (belonging to immunotype C), were selected to characterize their phylogenetic relationship, HBGA binding profiles and antigenic relatedness within (intra-immunotype), and between (inter-immunotypes) genotypes using mouse sera and patient's serum samples from the GI.3 related outbreak. Wide HBGA binding profiles and evolution of binding affinity were observed in the three GI genotypes studied. A low specific blockade antibody to GI.3 in the population generated the pool of susceptible individuals and supported virus spread in the outbreak. We found strong blockade immune response in homologous strains, moderate intra-immunotype blockade but weak inter-immunotypes blockade in humans following GI.3 norovirus infections. These findings further support the immunotypes grouping and will be valuable for optimizing the design of norovirus vaccine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752868PMC
http://dx.doi.org/10.3389/fmicb.2020.607723DOI Listing

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