Genetic point mutation inducing antigenic drift in hypervariable region of a very virulent IBDV isolate in chickens in Egypt during 2014-2016

H. Ellakany, A. Elbestawy, A. Sayed-Ahmed, S. Elgammal, A. Gado, Hatem Abdel-Hameed
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Abstract

Infectious bursal disease (IBD) is a highly contagious viral disease affecting young chickens causing immune suppression, high morbidity and mortality. Its economic significance is recognized worldwide. In this study, suspected IBD samples (bursa of Fabricious) were collected from 45 chicken flocks in 3 Egyptian governorates from 2014 to 2016. The virus was inoculated in embryonated chicken eggs via chorio-allantoic- membrane (CAM) route inducing specific IBDV lesions in the embryos. Viral identification was carried out through Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) targeting VP2 gene. Fourteen positive IBDV isolates (31%) were confirmed by RT-PCR. Three pure IBDV isolates were subjected to partial VP2 gene sequence analysis from which 2 IBDV isolates No. 1 and 3 (Accession No. KX827589.1 and MK906027) were defined as a very virulent IBDV (vvIBDV) genogroup 3, while the third isolate (Accession No. KX827588.1) was closely related to a vaccine strain in cvIBDV genogroup 1. Nucleotide and amino acid sequence analysis and blast of the IBDV isolates indicated a close relationship with the previously recorded Egyptian IBDVs with 96 to 99% identity. Point mutation or amino acid substitution in positions P202M (conserved region); and A211T, D212Y (hypervariable region) of the VP2 gene in the isolate No. 3 vvIBDV (Accession No. MK906027) that differ from all the previously recorded Egyptian isolates in GenBank were present.
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2014-2016年埃及一株强毒IBDV高变区基因点突变诱导抗原漂移
传染性法氏囊病(IBD)是一种影响雏鸡的高传染性病毒性疾病,可引起免疫抑制,发病率和死亡率高。它的经济意义是举世公认的。在本研究中,从2014年至2016年埃及3个省的45个鸡群中收集了疑似IBD样本(法氏囊)。该病毒通过绒毛膜-尿囊膜(CAM)途径接种于鸡胚,在胚中诱导特异性IBDV病变。通过针对VP2基因的逆转录聚合酶链反应(RT-PCR)进行病毒鉴定。RT-PCR结果证实14株IBDV阳性(31%)。对3株IBDV纯分离株进行了部分VP2基因序列分析,其中2株IBDV 1号和3号分离株(Accession No. 1;KX827589.1和MK906027)被定义为非常毒力IBDV (vvIBDV)基因组3;KX827588.1)与cvIBDV基因1组疫苗株密切相关。对分离株的核苷酸、氨基酸序列分析和blast分析表明,分离株与先前记录的埃及IBDV亲缘关系密切,同源性为96% ~ 99%。P202M(保守区)点突变或氨基酸取代;分离物3号vvIBDV中VP2基因的A211T, D212Y(高变区)。MK906027)与GenBank中先前记录的所有埃及分离株不同。
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