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The Lyssavirus glycoprotein: A key to cross-immunity
- Source :
- Virology. 498:250-256
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Rabies is an acute viral encephalomyelitis in warm-blooded vertebrates, caused by viruses belonging to Rhabdovirus family and genus Lyssavirus. Although rabies is categorised as a neglected disease, the rabies virus (RABV) is the most studied amongst Lyssaviruses which show nearly identical infection patterns. In efforts to improving post-exposure prophylaxis, several anti-rabies monoclonal antibodies (mAbs) targeting the glycoprotein (G protein) sites I, II, III and G5 have been characterized. To explore cross-neutralization capacity of available mAbs and discover new possible B-cell epitopes, we have analyzed all available glycoprotein sequences from Lyssaviruses with a focus on sequence variation and conservation. This information was mapped on the structure of a representative G protein. We proposed several possible cross-neutralizing B-cell epitopes (GUVTTTF, WLRTV, REECLD and EHLVVEEL) in complement to the already well-characterized antigenic sites. The research could facilitate development of novel cross-reactive mAbs against RABV and even more broad, against possibly all Lyssavirus members.
- Subjects :
- Models, Molecular
0301 basic medicine
Protein Conformation
Cross immunity
Cross Reactions
Antibodies, Viral
medicine.disease_cause
Epitope
Conserved sequence
Viral Proteins
03 medical and health sciences
Neutralization Tests
Rhabdoviridae Infections
Virology
medicine
Antigens, Viral
Lyssavirus
Conserved Sequence
Phylogeny
Glycoproteins
chemistry.chemical_classification
biology
Rabies virus
biology.organism_classification
medicine.disease
Antibodies, Neutralizing
030104 developmental biology
chemistry
biology.protein
Epitopes, B-Lymphocyte
Rabies
Antibody
Glycoprotein
Subjects
Details
- ISSN :
- 00426822
- Volume :
- 498
- Database :
- OpenAIRE
- Journal :
- Virology
- Accession number :
- edsair.doi.dedup.....10b908599a4f5218b30f6374123d6208
- Full Text :
- https://doi.org/10.1016/j.virol.2016.08.034