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

被引:107
作者
Eterradossi, N
Arnauld, C
Tekaia, F
Toquin, D
Le Coq, H
Rivallan, G
Guittet, M
Domenech, J
van den Berg, TP
Skinner, MA
机构
[1] Ctr Natl Etud Vet & Alimentaires, F-22440 Ploufragan, France
[2] Inst Pasteur, F-75724 Paris 15, France
[3] Lab Pathol Anim, Bingerville, Cote Ivoire
[4] Inst Natl Rech Vet, B-1180 Brussels, Belgium
[5] Inst Anim Hlth, Newbury RG20 7NN, Berks, England
关键词
D O I
10.1080/03079459995028
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The antigenic and genetic relationships between very virulent (vv) infectious bursal disease viruses (IBDV) from different countries were investigated. Antigenic characterization was performed using an antigen-capture ELISA based on a panel of seven neutralizing monoclonal antibodies (Mabs), which probe at least three VP2-located antigenic domains. All these domains are reactive in the Faragher 52/70 (F52/70) reference strain for European classical serotype 1 IBDV, Genomic characterization was achieved by reverse transcription, amplification and direct sequencing of a genome fragment encoding the VP2 variable domain. Eleven vv isolates from France were compared to the 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 antigenic profiles characterized by no binding of Mabs 3 and 4, Lack of binding 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 French isolates, which did not bind Mabs 6, 7 or 8, The genetic analysis revealed 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 acid differences to all the European viruses, including the F52/70 virus. Phylogenetic analysis based on the neighbour-joining and parsimony methods suggest that the African virus may belong to a genetically distinct lineage of highly pathogenic IBDVs.
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页码:36 / 46
页数:11
相关论文
共 34 条
[1]   DELETION MAPPING AND EXPRESSION IN ESCHERICHIA-COLI OF THE LARGE GENOMIC SEGMENT OF A BIRNAVIRUS [J].
AZAD, AA ;
JAGADISH, MN ;
BROWN, MA ;
HUDSON, PJ .
VIROLOGY, 1987, 161 (01) :145-152
[2]  
BAYLISS CD, 1990, J GEN VIROL, V71, P569
[3]   Molecular epidemiological tools and phylogenetic analysis of bacteria and viruses with special emphasis on lyssaviruses [J].
Bourhy, H ;
Kissi, B ;
Tordo, N ;
Badrane, H ;
Sacramento, D .
PREVENTIVE VETERINARY MEDICINE, 1995, 25 (02) :161-181
[4]  
Box P, 1989, WORLD POULTRY, V53, P17
[5]   VP2 SEQUENCES OF RECENT EUROPEAN VERY VIRULENT ISOLATES OF INFECTIOUS BURSAL DISEASE VIRUS ARE CLOSELY-RELATED TO EACH OTHER BUT ARE DISTINCT FROM THOSE OF CLASSICAL STRAINS [J].
BROWN, MD ;
GREEN, P ;
SKINNER, MA .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :675-680
[6]   Coding sequences of both genome segments of a European 'very virulunt' infectious bursal disease virus [J].
Brown, MD ;
Skinner, MA .
VIRUS RESEARCH, 1996, 40 (01) :1-15
[7]   OUTBREAK OF VIRULENT INFECTIOUS BURSAL DISEASE IN EAST ANGLIA [J].
CHETTLE, N ;
STUART, JC ;
WYETH, PJ .
VETERINARY RECORD, 1989, 125 (10) :271-272
[8]  
CISSE B, 1989, THESIS NATL SCH VET
[9]  
DOBOS P, 1995, VIRUS TAXONOMY, P240
[10]   Critical amino acid changes in VP2 variable domain are associated with typical and atypical antigenicity in very virulent infectious bursal disease viruses [J].
Eterradossi, N ;
Arnauld, C ;
Toquin, D ;
Rivallan, G .
ARCHIVES OF VIROLOGY, 1998, 143 (08) :1627-1636