首页> 外文期刊>Polish journal of veterinary sciences >Genetic characterization of Infectious Bursal Disease Viruses isolated from the vaccinated broiler chicken flocks in Egypt during 2015-2016
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Genetic characterization of Infectious Bursal Disease Viruses isolated from the vaccinated broiler chicken flocks in Egypt during 2015-2016

机译:2015 - 2016年埃及疫苗的肉鸡鸡群中分离出感染性Bursal疾病病毒的遗传表征

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The present study was conducted to characterize the infectious bursal disease virus (IBDV) circulating in clinically diseased broiler chicken flocks with previous vaccination history during 2015-2016 in Egypt. IBDVs were isolated from 48 out of 63 of the investigated bursae from 10 flocks onto embryonated chicken eggs (ECEs) and verified by reverse transcriptase-polymerase chain reaction (RF-PCR). Histopathologically, bursae lesions revealed some lymphocytes depletion as well as the presence of vesicles in the lining epithelium. The hyper variable region (HVR) of VP2 and VP1 genes of the 10 isolates (1 isolate/flock) were partially sequenced and subjected to comparative alignment and phyologenetic analysis. Phylogenetically, IBDV isolates were clustered into two distinct genetic lineages: variants of classical virulent (cv) and very virulent (vv) IBDV strains based on VP1 and VP2 amino acid (aa) sequences. Alignment analysis of IIVR-VP2 aa sequences has demonstrated that the vvIBDV isolates have the conserved residues of the vvIBDV pathotype (A222, I242, and I256), while, the cvIBDV isolates have the same aa sequences of the classical attenuated vaccine strain (D78). Expected single point mutation occurred at position 253 (H253N). All previously characterized isolates were re-subjected to molecular analysis with VP1 protein due to its correlation with virulence and pathogenicity of IBDVs. vvIBDV isolates have the conserved tripeptide (TDN), while, the cvIBDV isolates have aa substitutions at conserved tripeptide including NEG at 145-147 amino acid. The present study has demonstrated that variants of classical virulent and very virulent IBDV circulated among vaccinated flocks in Egypt during 2015-2016.
机译:本研究旨在描述2015-2016年期间在埃及有接种史的临床患病肉鸡群中传播的传染性法氏囊病病毒(IBDV)的特征。从10个鸡群63个法氏囊中的48个分离到IBDV,并通过逆转录聚合酶链反应(RF-PCR)进行验证。组织病理学检查,法氏囊损伤显示一些淋巴细胞缺失,以及衬里上皮中存在小泡。对10个分离物(1个分离物/群)的VP2和VP1基因的高变区(HVR)进行部分测序,并进行比较比对和植物学分析。在系统发育学上,IBDV分离株分为两个不同的遗传谱系:基于VP1和VP2氨基酸(aa)序列的经典强毒株(cv)和极强毒株(vv)变种。IIVR-VP2 aa序列的比对分析表明,vvIBDV分离株具有vvIBDV致病型(A222、I242和I256)的保守残基,而cvIBDV分离株具有与经典减毒疫苗株(D78)相同的aa序列。预期的单点突变发生在253位(H253N)。由于VP1蛋白与IBDV的毒力和致病性相关,所有先前鉴定的分离株都重新进行了分子分析。vvIBDV分离株具有保守的三肽(TDN),而cvIBDV分离株在145-147个氨基酸的保守三肽处具有aa取代,包括NEG。目前的研究表明,2015-2016年期间,埃及接种疫苗的群体中传播了经典毒力和极强毒力的IBDV变种。

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