Molecular characterization and phylogenetic analysis of very virulent infectious bursal disease virus circulating in Morocco during 2016-2017

被引:12
作者
Drissi Touzani, Charifa [1 ,2 ]
Fellahi, Siham [1 ]
Gaboun, Fatima [2 ]
Fassi Fihri, Ouafaa [1 ]
Baschieri, Selene [3 ]
Mentag, Rachid [2 ]
El Houadfi, Mohammed [1 ]
机构
[1] IAV Hassan II, Rabat Inst, Dept Pathol & Sante Publ Vet, Unite Pathol Aviaire, BP 6202, Rabat 10000, Morocco
[2] INRA, CRRA Rabat, Unite Biotechnol, Rabat Inst, Ave Mohamed Belarbi Alaoui,BP 6356, Rabat 10101, Morocco
[3] Agenzia Nazl Nuove Tecnol Energia & Sviluppo Econ, Biotechnol Lab, CR Casaccia, Via Anguillarese 301, I-00123 Rome, Italy
关键词
VP2; GENE; PATHOGENICITY; ANTIGENICITY; SEQUENCES; CHICKENS; GENOTYPE; STRAINS; TISSUE;
D O I
10.1007/s00705-018-4076-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Very virulent infectious bursal disease virus (vvIBDV), the cause of significant economic losses in many poultry-producing areas, has been present in Morocco since 1991. In spite of the introduction of vaccination, disease outbreaks are frequently observed. To ascertain if vaccines failure may be due to the emergence of new strains, the aim of this study was to perform for the first time the molecular characterization of vvIBDV strains circulating in Morocco by focusing on the hypervariable region (HVR) of the VP2 protein, which is frequently used for molecular epidemiology and phylogenetic studies. Field samples of haemorrhagicbursae of Fabricius were collected for molecular characterization in different parts of the country during 2016-2017 from 48 chicken flocks showing symptoms of disease. In a phylogenetic tree, nucleotide sequences containing the VP2 HVR of 13 samples that were positive for vvIBDV formed a common branch with those of vvIBDV references strains published in GenBank, but they clearly grouped into a distinct subcluster. An alignment of the deduced amino acid sequences, in addition to confirming the presence of the signature typical of the vvIBDV HVR, also revealed the presence of substitutions in hydrophilic loops that are known to be involved in the elicitation of neutralizing antibodies. One of these substitutions is unique to the Moroccan isolates. These results represent the first molecular characterization of vvIBDV isolates in Morocco and may indicate that one of the causes of vaccine ineffectiveness is antigenic drift.
引用
收藏
页码:381 / 390
页数:10
相关论文
共 34 条
[1]   A COMPARISON OF THE SEQUENCES OF SEGMENT-A OF 4 INFECTIOUS BURSAL DISEASE VIRUS-STRAINS AND IDENTIFICATION OF A VARIABLE REGION IN VP2 [J].
BAYLISS, CD ;
SPIES, U ;
SHAW, K ;
PETERS, RW ;
PAPAGEORGIOU, A ;
MULLER, H ;
BOURSNELL, MEG .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :1303-1312
[2]   Molecular determinants of virulence, cell tropism, and pathogenic phenotype of infectious bursal disease virus [J].
Brandt, M ;
Yao, K ;
Liu, MH ;
Heckert, RA ;
Vakharia, VN .
JOURNAL OF VIROLOGY, 2001, 75 (24) :11974-11982
[3]   AN APPARENTLY NEW DISEASE OF CHICKENS - AVIAN NEPHROSIS [J].
COSGROVE, AS .
AVIAN DISEASES, 1962, 6 (03) :385-&
[4]   Crystal Structure of an Aquabirnavirus Particle: Insights into Antigenic Diversity and Virulence Determinism [J].
Coulibaly, Fasseli ;
Chevalier, Christophe ;
Delmas, Bernard ;
Rey, Felix A. .
JOURNAL OF VIROLOGY, 2010, 84 (04) :1792-1799
[5]   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
[6]  
Hall T., 1999, NUCL ACIDS S SER, V41, P95
[7]   SEQUENCE-ANALYSIS AND EXPRESSION OF THE HOST-PROTECTIVE IMMUNOGEN-VP2 OF A VARIANT STRAIN OF INFECTIOUS BURSAL DISEASE VIRUS WHICH CAN CIRCUMVENT VACCINATION WITH STANDARD TYPE-I STRAINS [J].
HEINE, HG ;
HARITOU, M ;
FAILLA, P ;
FAHEY, K ;
AZAD, A .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :1835-1843
[8]   Pathogenicity of SspI-positive infectious bursal disease virus and molecular characterization of the VP2 hypervariable region [J].
Hoque, MM ;
Omar, AR ;
Chong, LK ;
Hair-Bejo, M ;
Aini, I .
AVIAN PATHOLOGY, 2001, 30 (04) :369-380
[9]   Studies on naturally occurring infectious bursal disease viruses suggest that a single amino acid substitution at position 253 in VP2 increases pathogenicity [J].
Jackwood, D. J. ;
Sreedevi, B. ;
LeFever, L. J. ;
Sommer-Wagner, S. E. .
VIROLOGY, 2008, 377 (01) :110-116
[10]   Genetic characteristics of infectious bursal disease viruses from four continents [J].
Jackwood, Daral J. ;
Sommer-Wagner, Susan .
VIROLOGY, 2007, 365 (02) :369-375