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Host-Range Shift Between Emerging P[8]-4 Rotavirus and Common P[8] and P[4] Strains
Amira Khachou1,2, Béatrice Le Moullac-Vaidye1, Cécile Peltier3,4
1Centre de Recherche en Cancérologie et Immunologie, Inserm, Université de Nantes, Centre Hospitalier Universitaire de Nantes, Nantes, France.
The Journal of Infectious Diseases
|March 20, 2020
Summary
Rotavirus strains P[8]-3 and P[4] infect secretor children, while the P[8]-4 strain targets nonsecretors. This difference in rotavirus tropism is linked to the FUT2 enzyme deficiency common in the population.
Area of Science:
- Virology
- Human Genetics
- Epidemiology
Background:
- Rotavirus is a leading cause of severe gastroenteritis in young children worldwide.
- Rotavirus strains are classified by their G and P types, with P[8] being a common type.
- The secretor histo-blood group phenotype, determined by the FUT2 gene, influences susceptibility to certain infections.
Purpose of the Study:
- To investigate the association between rotavirus P-types and secretor status in Tunisian children with gastroenteritis.
- To characterize the binding properties of different P[8] rotavirus VP8* proteins to host glycans.
Main Methods:
- Genotyping of rotavirus strains from children with gastroenteritis.
- Determination of secretor/nonsecretor phenotype of patients.
- In vitro binding assays of rotavirus VP8* proteins to saliva glycans.
Main Results:
- Rotavirus P[8]-3 and P[4] strains were associated with the secretor phenotype.
- The emerging P[8]-4 strain, accounting for 10% of cases, was found exclusively in nonsecretor patients.
- The P[8]-4 VP8* protein exhibited binding to glycans irrespective of secretor status, unlike P[8]-3 and P[4] strains.
Conclusions:
- The study identifies distinct tropisms for different P[8] rotavirus strains based on host secretor status.
- A high prevalence of nonsecretor phenotype in the Tunisian population may facilitate the co-circulation of P[8]-3 and P[8]-4 strains in respective secretor and nonsecretor children.
- These findings have implications for understanding rotavirus epidemiology and vaccine development.
Keywords:
FUT2fucosyltransferasegenetic susceptibilityhisto-blood group antigenhost rangerotavirussecretor/nonsecretor phenotypes
