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Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso

Norovirus (NoV) constitutes the second most common viral pathogen causing pediatric diarrhea after rotavirus. In Africa, diarrhea is a major health problem in children, and yet few studies have been performed regarding NoV. The association of histo-blood group antigens (HBGA) and susceptibility to N...

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Autores principales: Nordgren, Johan, Nitiema, Léon W., Ouermi, Djeneba, Simpore, Jacques, Svensson, Lennart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716642/
https://www.ncbi.nlm.nih.gov/pubmed/23894502
http://dx.doi.org/10.1371/journal.pone.0069557
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author Nordgren, Johan
Nitiema, Léon W.
Ouermi, Djeneba
Simpore, Jacques
Svensson, Lennart
author_facet Nordgren, Johan
Nitiema, Léon W.
Ouermi, Djeneba
Simpore, Jacques
Svensson, Lennart
author_sort Nordgren, Johan
collection PubMed
description Norovirus (NoV) constitutes the second most common viral pathogen causing pediatric diarrhea after rotavirus. In Africa, diarrhea is a major health problem in children, and yet few studies have been performed regarding NoV. The association of histo-blood group antigens (HBGA) and susceptibility to NoV infection is well established in Caucasian populations with non-secretors being resistant to many common NoV strains. No study regarding HBGA and NoV susceptibility has yet been performed in Africa. We collected 309 stool and 208 saliva samples from diarrheal children in Ouagadougou, Burkina Faso; May 2009 to March 2010. NoV was detected using real-time PCR, and genotyped by sequencing. Saliva samples were ABO, Lewis and secretor phenotyped using in house ELISA assays. NoV was detected in 12% (n = 37) of the samples. The genotype diversity was unusually large; overall the 37 positive samples belonged to 14 genotypes. Only children <2 years of age were NoV positive and the GII.4 NoVs were more frequent in the late dry season (Jan-May). NoV infections were observed less in children with the secretor-negative phenotype or blood group A (OR 0.18; p = 0.012 and OR 0.31; p = 0.054; respectively), with two non-secretors infected with genotypes GII.7 and GII.4 respectively. Lewis-negative (Le(a−b−)) children, representing 32% of the study population, were susceptible to GII, but were not infected with any NoV GI. GII.4 strains preferentially infected children with blood group B whereas secretor-positive children with blood group O were infected with the largest variety of genotypes. This is the first study identifying host genetic factors associated with susceptibility to NoV in an African population, and suggests that while the non-secretor phenotype provides protection; the Lewis b antigen is not necessary for GII infection.
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spelling pubmed-37166422013-07-26 Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso Nordgren, Johan Nitiema, Léon W. Ouermi, Djeneba Simpore, Jacques Svensson, Lennart PLoS One Research Article Norovirus (NoV) constitutes the second most common viral pathogen causing pediatric diarrhea after rotavirus. In Africa, diarrhea is a major health problem in children, and yet few studies have been performed regarding NoV. The association of histo-blood group antigens (HBGA) and susceptibility to NoV infection is well established in Caucasian populations with non-secretors being resistant to many common NoV strains. No study regarding HBGA and NoV susceptibility has yet been performed in Africa. We collected 309 stool and 208 saliva samples from diarrheal children in Ouagadougou, Burkina Faso; May 2009 to March 2010. NoV was detected using real-time PCR, and genotyped by sequencing. Saliva samples were ABO, Lewis and secretor phenotyped using in house ELISA assays. NoV was detected in 12% (n = 37) of the samples. The genotype diversity was unusually large; overall the 37 positive samples belonged to 14 genotypes. Only children <2 years of age were NoV positive and the GII.4 NoVs were more frequent in the late dry season (Jan-May). NoV infections were observed less in children with the secretor-negative phenotype or blood group A (OR 0.18; p = 0.012 and OR 0.31; p = 0.054; respectively), with two non-secretors infected with genotypes GII.7 and GII.4 respectively. Lewis-negative (Le(a−b−)) children, representing 32% of the study population, were susceptible to GII, but were not infected with any NoV GI. GII.4 strains preferentially infected children with blood group B whereas secretor-positive children with blood group O were infected with the largest variety of genotypes. This is the first study identifying host genetic factors associated with susceptibility to NoV in an African population, and suggests that while the non-secretor phenotype provides protection; the Lewis b antigen is not necessary for GII infection. Public Library of Science 2013-07-19 /pmc/articles/PMC3716642/ /pubmed/23894502 http://dx.doi.org/10.1371/journal.pone.0069557 Text en © 2013 Nordgren et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nordgren, Johan
Nitiema, Léon W.
Ouermi, Djeneba
Simpore, Jacques
Svensson, Lennart
Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso
title Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso
title_full Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso
title_fullStr Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso
title_full_unstemmed Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso
title_short Host Genetic Factors Affect Susceptibility to Norovirus Infections in Burkina Faso
title_sort host genetic factors affect susceptibility to norovirus infections in burkina faso
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716642/
https://www.ncbi.nlm.nih.gov/pubmed/23894502
http://dx.doi.org/10.1371/journal.pone.0069557
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