| Literature DB >> 27614701 |
Sindisiwe G Buthelezi1, Heini W Dirr2, Ereck Chakauya3, Rachel Chikwamba3, Lennart Martens4, Tsepo L Tsekoa3, Stoyan H Stoychev5, Elien Vandermarliere6.
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.Entities:
Keywords: Cross-neutralization; Glycoprotein; Lyssavirus; Rabies
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Year: 2016 PMID: 27614701 DOI: 10.1016/j.virol.2016.08.034
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616