Key result
Among children with acute diarrhea, rotavirus and norovirus predominantly infected those with secretor status, indicating higher susceptibility than non-secretors.
Why the study?
Host susceptibility according to human histo-blood group antigens is less described for rotavirus than norovirus, with variable HBGA polymorphisms across populations.
Cross-Sectional (n=272)
Secretor status is associated with higher susceptibility to both rotavirus and norovirus infections in children, with specific FUT3 polymorphisms reflecting the mixed Brazilian population.
Answers are grounded in this paper and cite their sources.
Secretor status was associated with higher symptomatic infection risk; extends HBGA susceptibility observations to mixed Brazilian populations but leaves practice implications open.
Host susceptibility according to human histo-blood group antigens (HBGAs) is widely known for norovirus infection, but is less described for rotavirus. Due to the variable HBGA polymorphism among populations, we aimed to evaluate the association between HBGA phenotypes (ABH, Lewis and secretor status) and susceptibility to rotavirus and norovirus symptomatic infection, and the polymorphisms of FUT2 and FUT3, of children from southeastern Brazil. Paired fecal-buccal specimens from 272 children with acute diarrhea were used to determine rotavirus/norovirus genotypes and HBGAs phenotypes/genotypes, respectively. Altogether, 100 (36.8%) children were infected with rotavirus and norovirus. The rotavirus P[8] genotype predominates (85.7%). Most of the noroviruses (93.8%) belonged to genogroup II (GII). GII.4 Sydney represented 76% (35/46) amongst five other genotypes. Rotavirus and noroviruses infected predominantly children with secretor status (97% and 98.5%, respectively). However, fewer rotavirus-infected children were Lewis-negative (8.6%) than the norovirus-infected ones (18.5%). FUT3 single nucleotide polymorphisms (SNP) occurred mostly at the T59G > G508A > T202C > C314T positions. Our results reinforce the current knowledge that secretors are more susceptible to infection by both rotavirus and norovirus than non-secretors. The high rate for Lewis negative (17.1%) and the combination of SNPs, beyond the secretor status, may reflect the highly mixed population in Brazil.
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Tonini et al. (2020) conducted a cross-sectional in Acute diarrhea (n=272). Secretor status (HBGA phenotypes) vs. Non-secretor status was evaluated on Rotavirus and norovirus symptomatic infection. Among children with acute diarrhea, rotavirus and norovirus predominantly infected those with secretor status, indicating higher susceptibility than non-secretors.
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