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A Comparative Approach to Characterize the Landscape of Host-Pathogen Protein-Protein Interactions
Published on: July 18, 2013
Host-pathogen co-evolution and glycan interactions.
Jacques Le Pendu1, Kristina Nyström1, Nathalie Ruvoën-Clouet2
1Inserm, UMR 892; CNRS, UMR 6299; Université de Nantes, IRS UN, 8 Quai Moncousu, BP 70721, 44007 Nantes cedex 1, France.
Noroviruses and rotavirus A utilize histo-blood group antigens (HBGAs) for infection. Host HBGA diversity creates herd innate protection, maintaining virus circulation while partially protecting the population.
Area of Science:
- Virology
- Immunology
- Evolutionary Biology
Background:
- Noroviruses and rotavirus A attach to host histo-blood group antigens (HBGAs).
- HBGA polymorphism in humans leads to varied susceptibility to different virus strains.
- This variation suggests a co-evolutionary trade-off maintaining both host protection and virus spread.
Purpose of the Study:
- To explore the co-evolutionary dynamics between caliciviruses, specifically RHDV, and host HBGA diversity.
- To understand how HBGA polymorphism contributes to herd innate protection.
- To use RHDV as a model for studying virus-host co-evolution involving glycan recognition.
Main Methods:
- Analysis of HBGA binding specificities of norovirus and rotavirus strains.
- Examination of field observations documenting virus evolution and host HBGA phenotype selection.
- Modeling of virus-host interactions based on glycan polymorphisms.
Main Results:
- Norovirus strains collectively infect the human population but individually infect subgroups.
- Host HBGA diversity provides partial population-level protection ('Herd Innate Protection').
- Evidence of reciprocal evolution: viruses adapting to HBGA diversity and hosts selected by virus outbreaks.
Conclusions:
- HBGA polymorphism is a key factor in the co-evolutionary relationship between humans and caliciviruses.
- Herd innate protection, driven by HBGA diversity, balances host defense and pathogen persistence.
- RHDV serves as a valuable model for understanding virus-host co-evolutionary processes involving glycans.
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