在埃及接种疫苗的家禽中出现了新的传染性法氏囊病病毒变体

Momtaz A Shahin, Hesham A Sultan, Ali Zanaty, Zienab Mosaad, Naglaa M Hagage, Amany Adel, Karim Selim, Dalia Saied, Abdel Hafez Samir, Ahmed Erfan, Abdelsatar Arafa, Abdullah Selim, Mohammed Samy, Mahmoud M Naguib, Heba Hassan, Osama El Shazly, Zeinab A Elbade, Mahmoud Kamel, Eman Farghaly, Samah Eid, Mohamed El Shahaby, Mohamed Hammoda, Osama Mehana, Mohamed Nabeh, Ahmed Samy
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引用次数: 0

摘要

传染性法氏囊病病毒(IBDVs)对全世界的家禽生产有着深远的影响,直接导致高达100%的死亡率,并通过其免疫抑制作用间接造成死亡率。自从1999年底在埃及出现经过抗原性修饰的非常强毒的IBDV (vvIBDV)以来,该国经历了高死亡率和典型的vvIBDV大体病变的反复暴发。然而,2023年发生了显著的变化,其特征是报告的亚临床IBDV病例大幅增加,表现为囊萎缩和相关的免疫抑制。为了评估现场情况,我们检查了2023年21个农场和2021年和2022年18个农场的样本,根据临床诊断,这些农场都经历了IBD暴发。这些样本被提交到我们的实验室进行确认测试,随后进行VP2-HVR测序。系统发育分析显示,2021年和2022年收集的所有样本均聚集了经典强毒株和极强毒株。2023年,1份样本聚集为埃及型vvIBDV, 1份样本聚集为经典毒力型IBDV,其余2023份样本聚集为中国新型IBDV (nVarIBDV)。VP2的氨基酸序列比对表明,所有埃及经典毒力菌株与Winterfield或Leukert菌株相似。相比之下,vvIBDV株在埃及抗原性非典型vvIBDV中发现的三个典型残基中有两个,即Y220F和G254S,但没有A321T,并且一个样本与欧洲vvIBDV(1989年出现)相同。与此同时,本研究识别的所有变异菌株除了在中国变异IBDV中发现的3个保守氨基酸残基外,均具有变异IBDV的典型残基。然而,所有埃及变种菌株在321 (321V)位置显示突变,这是衣壳最暴露的部分,已知对IBDV抗原性有巨大影响,除了一个样本有318G。本报告强调了在埃及出现的与中国新变体聚集的新型IBDV,引起囊萎缩并在广泛的地理距离上亚临床地在肉鸡养殖场传播,由于免疫抑制导致巨大的经济损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emergence of the Novel Infectious bursal disease viruse Variant in Vaccinated Poultry Flocks in Egypt
Infectious bursal disease viruses (IBDVs) have a profound impact on poultry production worldwide, directly causing mortality rates of up to 100%, and indirectly through their immunosuppressive effects. Since the emergence of the antigenically modified very virulent IBDV (vvIBDV) in Egypt in late 1999, the country has experienced recurrent outbreaks with high mortality rates and typical vvIBDV gross lesions. However, a notable shift occurred in 2023, characterized by a substantial increase in reported subclinical IBDV cases exhibiting atrophied bursa and associated immunosuppression. To assess the field situation, we examined samples from 21 farms in 2023 and 18 farms from 2021 and 2022, all of which experienced IBD outbreaks based on clinical diagnosis. These samples were submitted to our laboratory for confirmatory testing and subsequently subjected to VP2-HVR sequencing. Phylogenetic analysis revealed that all samples collected in 2021 and 2022 clustered with classical virulent strains and very virulent IBDV. In 2023, one sample clustered with the Egyptian vvIBDV, while one sample clustered with classic virulent IBDV, and the remaining 2023 samples clustered with the Chinese novel variant IBDV (nVarIBDV). The alignment of deduced amino acid sequences for VP2 revealed that all Egyptian classic virulent strains were similar to the Winterfield or Leukert strains. In contrast, vvIBDV strains exhibited two out of the three typical residues found in Egyptian antigenically atypical vvIBDV, namely Y220F and G254S, but not A321T, and one sample was identical to the European vvIBDV (emerged in 1989). Meanwhile, all variant strains recognized in the present study exhibited typical residues found in variant IBDV, in addition to the three conserved amino acid residues found only in Chinese variant IBDVs. However, all Egyptian variant strains showed a mutation at position 321 (321V), which represents the most exposed part of the capsid and is known to have a massive impact on IBDV antigenicity, with the exception of one sample that had 318G instead. This report highlights the emergence of a new variant IBDV clustered with the Chinese new variant in Egypt, causing bursa atrophy and spreading subclinically in broiler farms over a wide geographic distance, resulting in massive economic losses due to immunosuppression.
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