4.7 Article

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

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 225, Issue 1, Pages 105-115

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiab316

Keywords

birth cohort; histo-blood group antigens; incidence; Nicaragua; norovirus; secretor

Funding

  1. National Institute of Allergy and Infectious Diseases at the National Institute of Health [R01AI127845, K24AI141744]
  2. Fogarty International Center at the National Institute of Health [D43TW010923]
  3. Swedish Research Council [2014-02827, 2018-02862]
  4. Mucosa Infection and Inflammation Center at Linkoping University
  5. Swedish Research Council [2018-02862, 2014-02827] Funding Source: Swedish Research Council
  6. Vinnova [2018-02862] Funding Source: Vinnova

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This study found that histo-blood group status plays an important role in the burden and severity of norovirus gastroenteritis in young infants, with secretor children being more susceptible to GII norovirus and GII.4 causing more severe symptoms.
Background. The role of histo-blood group on the burden and severity of norovirus gastroenteritis in young infants has not been well documented. Methods. Norovirus gastroenteritis was assessed in 443 Nicaraguan children followed from birth until 3 years of age. Stool samples were tested for norovirus by reverse-transcription quantitative polymerase chain reaction (RT-qPCR), and histo-blood group antigens (HBGAs) were determined by phenotyping of saliva and blood. Hazard ratios and predictors of norovirus acute gastroenteritis (AGE) outcome stratified by HBGA were estimated using Cox proportional hazards models. Results. Of 1353 AGE episodes experienced by children, 229 (17%) tested positive for norovirus with an overall incidence of 21.9/100 child-years. Secretor children were infected as early as 2 months of age and had a higher incidence of norovirus GII compared to nonsecretor children (15.4 vs 4.1/100 child-years, P = .006). Furthermore, all GII.4 AGE episodes occurred in secretor children. Children infected with GI (adjusted odds ratio [aOR], 0.09 [95% confidence interval {CI}, .02-.33]) or non-GII.4 viruses (aOR, 0.2 [95% CI, .07-.6]) were less likely to have severe AGE compared to GII.4-infected children. Conclusions. Secretor status in children strongly influences the incidence of symptomatic norovirus infection in a genogroup or genotype-dependent manner and provides evidence that clinical severity in children depends on norovirus genotypes.

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