Michel Linda O, Jackwood Daral J
Food Animal Health Research Program, The Ohio State University/Ohio Agricultural Research and Development Center, 1680 Madison Ave., Wooster, OH, 44691, USA.
Department of Veterinary Preventive Medicine, The Ohio State University/Ohio Agricultural Research and Development Center, 1680 Madison Ave., Wooster, OH, 44691, USA.
Arch Virol. 2017 Dec;162(12):3661-3670. doi: 10.1007/s00705-017-3500-4. Epub 2017 Aug 19.
Infectious bursal disease virus (IBDV) causes infectious bursal disease (IBD), an immunosuppressive disease of poultry. The current classification scheme of IBDV is confusing because it is based on antigenic types (variant and classical) as well as pathotypes. Many of the amino acid changes differentiating these various classifications are found in a hypervariable region of the capsid protein VP2 (hvVP2), the major host protective antigen. Data from this study were used to propose a new classification scheme for IBDV based solely on genogroups identified from phylogenetic analysis of the hvVP2 of strains worldwide. Seven major genogroups were identified, some of which are geographically restricted and others that have global dispersion, such as genogroup 1. Genogroup 2 viruses are predominately distributed in North America, while genogroup 3 viruses are most often identified on other continents. Additionally, we have identified a population of genogroup 3 vvIBDV isolates that have an amino acid change from alanine to threonine at position 222 while maintaining other residues conserved in this genogroup (I242, I256 and I294). A222T is an important mutation because amino acid 222 is located in the first of four surface loops of hvVP2. A similar shift from proline to threonine at 222 is believed to play a role in the significant antigenic change of the genogroup 2 IBDV strains, suggesting that antigenic drift may be occurring in genogroup 3, possibly in response to antigenic pressure from vaccination.
传染性法氏囊病病毒(IBDV)可引发传染性法氏囊病(IBD),这是一种禽类的免疫抑制性疾病。目前IBDV的分类方案令人困惑,因为它基于抗原类型(变异型和经典型)以及致病型。区分这些不同分类的许多氨基酸变化都出现在衣壳蛋白VP2的高变区(hvVP2),这是主要的宿主保护性抗原。本研究的数据被用于提出一种仅基于对全球范围内毒株的hvVP2进行系统发育分析所确定的基因组的IBDV新分类方案。确定了七个主要基因组,其中一些在地理上受到限制,而其他一些则具有全球分布,如基因组1。基因组2病毒主要分布在北美,而基因组3病毒最常在其他大陆被鉴定到。此外,我们还鉴定出一群基因组3的vvIBDV分离株,它们在第222位氨基酸处有从丙氨酸到苏氨酸的变化,同时该基因组中的其他残基(I242、I256和I294)保持保守。A222T是一个重要的突变,因为第222位氨基酸位于hvVP2四个表面环中的第一个。据信在基因组2的IBDV毒株的显著抗原变化中,第222位从脯氨酸到苏氨酸的类似转变起到了作用,这表明基因组3可能正在发生抗原漂移,可能是对疫苗接种产生的抗原压力的反应。