Molecular characterization and pathogenicity of highly pathogenic fowl adenovirus serotype 4 isolated from laying flock with hydropericardium-hepatitis syndrome

被引:11
|
作者
Yin, Dongdong [1 ,2 ]
Xue, Mei [1 ,2 ]
Yang, Kankan [1 ,2 ]
Xiong, Xiuqi [1 ,2 ]
Geng, Shu [1 ,2 ]
Tu, Jian [1 ,2 ]
Song, Xiangjun [1 ,2 ]
Shao, Ying [1 ,2 ]
Wang, Guijun [1 ,2 ]
Qi, Kezong [1 ,2 ]
机构
[1] Anhui Agr Univ, Coll Anim Sci & Technol, Hefei 230036, Peoples R China
[2] Anhui Prov Key Lab Vet Pathobiol & Dis Control, Hefei 230036, Peoples R China
基金
中国国家自然科学基金;
关键词
Fowl adenovirus serotype 4; Hepatitis-hydropericardium syndrome; Phylogenetic analysis; Fiber-2; 100K protein; CHICKENS; PROTEIN; HEXON; OUTBREAKS; POULTRY; GENES;
D O I
10.1016/j.micpath.2020.104381
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hydropericardium-hepatitis syndrome (HHS) is an important emerging disease responsible for huge economic losses to the poultry industry in China. HHS primarily affects 20 to 60-day-old broilers and rarely occurs in laying flock. In this study, the highly pathogenic fowl adenovirus (FAdV) strain, AH-F19, was isolated from the liver samples of 120-day-old laying flock with HHS and its phylogenetic information, genetic mutations, and pathogenicity was evaluated. The phylogenetic analysis revealed that AH-F19 belonged to the FAdV serotype 4 (FAdV-4) cluster, however, 100K differs from the other FAdV-4 strains and is divided into different branches. Amino acid variations in fiber-2 for pathogenic isolates and non-pathogenic isolates indicated that D219, T300, and T380 may not be responsible for virulence. Animal experiments revealed AH-F19 to be a highly pathogenic isolate that can cause 100% mortality in three-week-old specific pathogen-free (SPF) chickens, which exhibited typical hydropericardium and hepatitis. Microscopically, the presence of basophilic intranuclear inclusion bodies in hepatocytes, fractured heart muscle fibers, as well as kidney degeneration and necrosis was observed. Collectively, these findings enriched our understanding of FAdV-4 pathogenicity and provided a reference for further exploration into its pathogenicity.
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页数:7
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