Literature DB >> 36121297

Intestinal Norovirus Binding Patterns in Nonsecretor Individuals.

Georges Tarris1,2, Marie Estienney3,2, Philippe Daval-Frérot3, Anne-Cécile Lariotte1, Damien Aubignat1, Karine Sé1, Christophe Michiels4, Laurent Martin1, Alexis de Rougemont3,2, Gaël Belliot3,2.   

Abstract

Human norovirus (HuNoV) infection is associated with an active FUT2 gene, which characterizes the secretor phenotype. However, nonsecretor individuals are also affected by HuNoV infection although in a lesser proportion. Here, we studied GII.3, GII.4, and GII.17 HuNoV interactions in nonsecretor individuals using virus-like particles (VLPs). Only GII.4 HuNoV specifically interacted with nonsecretor saliva. Competition experiments using histo-blood group antigen (HBGA)-specific monoclonal antibodies (MAbs) demonstrate that GII.4 VLPs recognized the Lewis a (Lea) antigen. We also analyzed HuNoV VLP interactions on duodenum tissue blocks from healthy nonsecretor individuals. VLP binding was observed for the three HuNoV genotypes in 10 of the 13 individuals, and competition experiments demonstrated that VLP recognition was driven by an interaction with the Lea antigen. In 3 individuals, binding was restricted to either GII.4 alone or GII.3 and GII.17. Finally, we performed a VLP binding assay on proximal and distal colon tissue blocks from a nonsecretor patient with Crohn's disease. VLP binding to inflammatory tissues was genotype specific since GII.4 and GII.17 VLPs were able to interact with regenerative mucosa, whereas GII.3 VLP was not. The binding of GII.4 and GII.17 HuNoV VLPs was linked to Lea in regenerative mucosae from the proximal and distal colon. Overall, our data clearly showed that Lea has a pivotal role in the recognition of HuNoV in nonsecretors. We also showed that Lea is expressed in inflammatory/regenerative tissues and interacts with HuNoV in a nonsecretor individual. The physiological and immunological consequences of such interactions in nonsecretors have yet to be elucidated. IMPORTANCE Human norovirus (HuNoV) is the main etiological agent of viral gastroenteritis in all age classes. HuNoV infection affects mainly secretor individuals where ABO(H) and Lewis histo-blood group antigens (HBGAs) are present in the small intestine. Nonsecretor individuals, who only express Lewis (Le) antigens, are less susceptible to HuNoV infection. Here, we studied the interaction of common HuNoV genotypes (GII.3, GII.4, and GII.17) in nonsecretor individuals using synthetic viral particles. Saliva binding assays showed that only GII.4 interacted with nonsecretor saliva via the Lewis a (Lea) antigen Surprisingly, the three genotypes interacted with nonsecretor enterocytes via the Lea antigen on duodenal tissue blocks, which were more relevant for HuNoV/HBGA studies. The Lea antigen also played a pivotal role in the recognition of GII.4 and GII.17 particles by inflammatory colon tissue from a nonsecretor Crohn's disease patient. The implications of HuNoV binding in nonsecretors remain to be elucidated in physiological and pathological conditions encountered in other intestinal diseases.

Entities:  

Keywords:  Crohn’s disease; FUT2; HBGA; colon; duodenum; healthy; nonsecretor; norovirus

Mesh:

Substances:

Year:  2022        PMID: 36121297      PMCID: PMC9555158          DOI: 10.1128/jvi.00865-22

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   6.549


  79 in total

1.  Relationship between GII.3 norovirus infections and blood group antigens in young children in Tunisia.

Authors:  S Ayouni; M Estienney; K Sdiri-Loulizi; K Ambert-Balay; A de Rougemont; S Aho; S Hammami; M Aouni; M N Guédiche; P Pothier; G Belliot
Journal:  Clin Microbiol Infect       Date:  2015-05-21       Impact factor: 8.067

2.  Comparison of human saliva and synthetic histo-blood group antigens usage as ligands in norovirus-like particle binding and blocking assays.

Authors:  Hanni Uusi-Kerttula; Kirsi Tamminen; Maria Malm; Timo Vesikari; Vesna Blazevic
Journal:  Microbes Infect       Date:  2014-03-14       Impact factor: 2.700

3.  Spike protein VP8* of human rotavirus recognizes histo-blood group antigens in a type-specific manner.

Authors:  Pengwei Huang; Ming Xia; Ming Tan; Weiming Zhong; Chao Wei; Leyi Wang; Ardythe Morrow; Xi Jiang
Journal:  J Virol       Date:  2012-02-15       Impact factor: 5.103

4.  Predicting susceptibility to norovirus GII.4 by use of a challenge model involving humans.

Authors:  Robert Frenck; David I Bernstein; Ming Xia; Pengwei Huang; Weiming Zhong; Susan Parker; Michelle Dickey; Monica McNeal; Xi Jiang
Journal:  J Infect Dis       Date:  2012-08-20       Impact factor: 5.226

5.  An immunohistochemical employer monoclonal antibodies against Le(a), sialyl Le(a), Le(x), and sialyl Le(x) antigens in primary colorectal, carcinomas and lymph node and hepatic lesions.

Authors:  T Nakagoe; K Fukushima; M Hirota; H Kusano; H Ayabe; M Tomita; S Kamihira
Journal:  J Gastroenterol       Date:  1994-04       Impact factor: 7.527

6.  Cell attachment protein VP8* of a human rotavirus specifically interacts with A-type histo-blood group antigen.

Authors:  Liya Hu; Sue E Crawford; Rita Czako; Nicolas W Cortes-Penfield; David F Smith; Jacques Le Pendu; Mary K Estes; B V Venkataram Prasad
Journal:  Nature       Date:  2012-04-15       Impact factor: 49.962

7.  Secretor Status Strongly Influences the Incidence of Symptomatic Norovirus Infection in a Genotype-Dependent Manner in a Nicaraguan Birth Cohort.

Authors:  Yaoska Reyes; Fredman González; Lester Gutiérrez; Patricia Blandón; Edwing Centeno; Omar Zepeda; Christian Toval-Ruíz; Lisa C Lindesmith; Ralph S Baric; Nadja Vielot; Marta Diez-Valcarce; Jan Vinjé; Lennart Svensson; Sylvia Becker-Dreps; Johan Nordgren; Filemón Bucardo
Journal:  J Infect Dis       Date:  2022-01-05       Impact factor: 7.759

8.  Mechanisms of GII.4 norovirus persistence in human populations.

Authors:  Lisa C Lindesmith; Eric F Donaldson; Anna D Lobue; Jennifer L Cannon; Du-Ping Zheng; Jan Vinje; Ralph S Baric
Journal:  PLoS Med       Date:  2008-02       Impact factor: 11.069

9.  An outbreak caused by GII.17 norovirus with a wide spectrum of HBGA-associated susceptibility.

Authors:  Xu-Fu Zhang; Qiong Huang; Yan Long; Xi Jiang; Ting Zhang; Ming Tan; Qiao-Li Zhang; Zhen-Yu Huang; Yue-Huan Li; Yao-Quan Ding; Gui-Fang Hu; Shixing Tang; Ying-Chun Dai
Journal:  Sci Rep       Date:  2015-12-07       Impact factor: 4.379

10.  Systematic sequence analysis of the FUT3 gene identifies 11 novel alleles in the Sindhi and Punjabi populations from Pakistan.

Authors:  Maomao Zhao; Atif Adnan; Allah Rakha; Shahid Nazir; Meihui Tian; Siyi Zhang; Hao Pang
Journal:  Sci Rep       Date:  2020-03-26       Impact factor: 4.379

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