Antigenic and genetic relationships between European very virulent infectious bursal disease viruses and an early West African isolate

Citation
N. Eterradossi et al., Antigenic and genetic relationships between European very virulent infectious bursal disease viruses and an early West African isolate, AVIAN PATH, 28(1), 1999, pp. 36-46
Citations number
34
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
AVIAN PATHOLOGY
ISSN journal
03079457 → ACNP
Volume
28
Issue
1
Year of publication
1999
Pages
36 - 46
Database
ISI
SICI code
0307-9457(199902)28:1<36:AAGRBE>2.0.ZU;2-I
Abstract
The antigenic and genetic relationships between very virulent (vv) infectio us bursal disease viruses (IBDV) from different countries were investigated . Antigenic characterization was performed using an antigen-capture ELISA b ased on a panel of seven neutralizing monoclonal antibodies (Mabs), which p robe at least three VP2-located antigenic domains. All these domains are re active in the Faragher 52/70 (F52/70) reference strain for European classic al serotype 1 IBDV, Genomic characterization was achieved by reverse transc ription, amplification and direct sequencing of a genome fragment encoding the VP2 variable domain. Eleven vv isolates from France were compared to th e British, Dutch and Belgian UK661, DV86 and 849VB viruses, and to an early vv isolate obtained from the Ivory Coast in 1988, All viruses exhibited an tigenic profiles characterized by no binding of Mabs 3 and 4, Lack of bindi ng of Mabs 3 and 4 might thus be helpful for differentiating classical and vvIBDVs, None of the non-French strains resembled the 91168 and 94432 Frenc h isolates, which did not bind Mabs 6, 7 or 8, The genetic analysis reveale d close relationships between all the European viruses, which differed from one another by no more than 12 nucleotides and 3 amino acids. The African isolate was markedly different, with at least 22 nucleotide and six amino a cid differences to all the European viruses, including the F52/70 virus. Ph ylogenetic analysis based on the neighbour-joining and parsimony methods su ggest that the African virus may belong to a genetically distinct lineage o f highly pathogenic IBDVs.