Department of Virology, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
Department of Hygiene and Zoonoses, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
Vet Res Commun. 2024 Oct;48(5):3089-3104. doi: 10.1007/s11259-024-10468-z. Epub 2024 Jul 30.
This study investigated the genotype classification and pathogenicity of infectious bursal disease virus (IBDV) circulating in vaccinated broiler chicken farms in Egypt. A total of 150 samples were collected from 30 vaccinated commercial broiler chicken farms and pooled into 30 working samples. IBDV was tested using reverse transcriptase polymerase chain reaction (RT-PCR) amplification of the hypervariable region of the viral protein 2 (hvVP2) and the VP1 gene 5' extremity. Both RT-PCR fragments were sequenced from six samples, and then the obtained nucleotide sequences were analyzed. The IBDV genotypes were identified using nucleotide sequences. Five sequences of the six strains examined were classified as genotype A3B2 for the highly virulent segments A and B (vv-A/vv-B IBDV). Interestingly, this study identified and classified a novel segment-reassortant strain as the A1B2 genotype. Specifically, it involved the segment reassortment of classical virulent segment A (cv-A) with vv-B producing cv-A/vv-B reassortant IBDV. Subsequently, we compared the pathogenicity of reassortant (cv-A/vv-B) IBDV and vvIBDV strains identified in this study. Both strains developed typical IBD clinical signs, postmortem lesions, histopathology, immunohistochemistry, and lesion scores, which were more severe in vvIBDV than reassortant IBDV. In conclusion, this is the first report of the genotype classification based on both genome segments (hvVP2 and VP1) with pathogenicity of IBDV circulating in vaccinated broiler chicken farms and this pathogenicity is more severe in vvIBDV strain than a novel reassortant IBDV strain.
本研究调查了在埃及接种疫苗的肉鸡场中流行的传染性法氏囊病病毒(IBDV)的基因型分类和致病性。从 30 个接种商业肉鸡场采集了 150 个样本,并将其汇集为 30 个工作样本。使用逆转录聚合酶链反应(RT-PCR)扩增病毒蛋白 2(hvVP2)和 VP1 基因 5'端的高变区来检测 IBDV。从六个样本中对两个 RT-PCR 片段进行了测序,然后对获得的核苷酸序列进行了分析。使用核苷酸序列鉴定 IBDV 基因型。在检查的六个毒株中,有五个序列被归类为高度致病毒株 A 和 B(vv-A/vv-B IBDV)的 A3B2 基因型。有趣的是,本研究鉴定并分类了一种新型的节段重组毒株为 A1B2 基因型。具体来说,它涉及到经典致病毒株 A(cv-A)与 vv-B 的节段重组,产生 cv-A/vv-B 重组 IBDV。随后,我们比较了本研究中鉴定的重组(cv-A/vv-B)IBDV 和 vvIBDV 株的致病性。两种毒株均表现出典型的 IBD 临床症状、死后病变、组织病理学、免疫组织化学和病变评分,vvIBDV 比重组 IBDV 更严重。总之,这是首次报告在接种疫苗的肉鸡场中流行的 IBDV 基于两个基因组节段(hvVP2 和 VP1)的基因型分类及其致病性,vvIBDV 株的致病性比新型重组 IBDV 株更严重。