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

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 gastroenteriti...

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Autores principales: Xie, Dongjie, Chen, Junrui, Yu, Jingrong, Pei, Fuyu, Koroma, Mark Momoh, Wang, Lu, Qiu, Mengsi, Hou, Yuzhen, Yu, Dexian, Zhang, Xu-Fu, Dai, Ying-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752868/
https://www.ncbi.nlm.nih.gov/pubmed/33363528
http://dx.doi.org/10.3389/fmicb.2020.607723
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author Xie, Dongjie
Chen, Junrui
Yu, Jingrong
Pei, Fuyu
Koroma, Mark Momoh
Wang, Lu
Qiu, Mengsi
Hou, Yuzhen
Yu, Dexian
Zhang, Xu-Fu
Dai, Ying-Chun
author_facet Xie, Dongjie
Chen, Junrui
Yu, Jingrong
Pei, Fuyu
Koroma, Mark Momoh
Wang, Lu
Qiu, Mengsi
Hou, Yuzhen
Yu, Dexian
Zhang, Xu-Fu
Dai, Ying-Chun
author_sort Xie, Dongjie
collection PubMed
description 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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spelling pubmed-77528682020-12-23 Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera Xie, Dongjie Chen, Junrui Yu, Jingrong Pei, Fuyu Koroma, Mark Momoh Wang, Lu Qiu, Mengsi Hou, Yuzhen Yu, Dexian Zhang, Xu-Fu Dai, Ying-Chun Front Microbiol Microbiology 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. Frontiers Media S.A. 2020-12-08 /pmc/articles/PMC7752868/ /pubmed/33363528 http://dx.doi.org/10.3389/fmicb.2020.607723 Text en Copyright © 2020 Xie, Chen, Yu, Pei, Koroma, Wang, Qiu, Hou, Yu, Zhang and Dai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Xie, Dongjie
Chen, Junrui
Yu, Jingrong
Pei, Fuyu
Koroma, Mark Momoh
Wang, Lu
Qiu, Mengsi
Hou, Yuzhen
Yu, Dexian
Zhang, Xu-Fu
Dai, Ying-Chun
Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera
title Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera
title_full Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera
title_fullStr Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera
title_full_unstemmed Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera
title_short Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera
title_sort characterization of antigenic relatedness among gi norovirus genotypes using serum samples from norovirus-infected patients and mouse sera
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752868/
https://www.ncbi.nlm.nih.gov/pubmed/33363528
http://dx.doi.org/10.3389/fmicb.2020.607723
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