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Infant Non-Secretor Histoblood Group Antigen Phenotype Reduces Susceptibility to Both Symptomatic and Asymptomatic
Benjamin Lee1, Md Abdul Kader2, Masud Alam2
1Department of Pediatrics, Vaccine Testing Center and Translational Global Infectious Diseases Research Center, Larner College of Medicine, University of Vermont, Burlington, VT 05405, USA.
Insights
Infant non-secretor status reduces the risk of asymptomatic rotavirus infection, similar to symptomatic cases. This suggests non-secretors are less susceptible to rotavirus infection overall.
Area of Science:
- Pediatrics
- Infectious Diseases
- Immunology
Background:
- Infant non-secretor phenotype is linked to lower symptomatic rotavirus diarrhea risk.
- The role of secretor status in asymptomatic rotavirus infections remains unclear.
Purpose of the Study:
- To investigate the association between infant secretor phenotype and asymptomatic rotavirus infection.
- To determine if secretor status influences rotavirus diarrhea risk in unvaccinated infants.
Main Methods:
- Nested case-control study within a birth cohort in Dhaka, Bangladesh.
- Secretor phenotyping of infant saliva and rotavirus testing of surveillance stools using RT-PCR, PCR, and sequencing.
Main Results:
- Infant non-secretors had significantly fewer asymptomatic rotavirus infections in the first year of life.
- The reduced risk appeared to be dependent on the rotavirus P-genotype.
Conclusions:
- Non-secretor status is associated with a reduced risk of acquiring rotavirus infection, irrespective of symptomatic presentation.
- This suggests decreased susceptibility to infection is the primary protective mechanism.
Abstract:
The infant non-secretor histoblood group antigen phenotype is associated with reduced risk of symptomatic rotavirus diarrhea, one of the leading global causes of severe pediatric diarrheal disease and mortality. However, little is known regarding the role of secretor status in asymptomatic rotavirus infections. Therefore, we performed a nested case-control study within a birth cohort study previously conducted in Dhaka, Bangladesh, to determine the association between infant secretor phenotype and the odds of asymptomatic rotavirus infection, in addition to the risk of rotavirus diarrhea, in unvaccinated infants. In the parent cohort, infants were enrolled in the first week of life and followed through the first two years of life with multiple clinic visits and active surveillance for diarrheal illness. Secretor phenotyping was performed on saliva. Eleven surveillance stools collected over the first year of life were tested for rotavirus by real-time RT-PCR, followed by conventional PCR and amplicon sequencing to identify the infecting P-type of positive specimens. Similar to findings for symptomatic diarrhea, infant non-secretors experienced significantly fewer primary episodes of asymptomatic rotavirus infection through the first year of life in a likely rotavirus P-genotype-dependent manner. These data suggest that non-secretors experienced reduced risk from rotavirus due to decreased susceptibility to infection rather than reduced infection severity.
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