Identification and Characterization of a Distinct Strain of Beak and Feather Disease Virus in Southeast China

被引:5
作者
Ma, Yanmei [1 ]
Chen, Xiaoyong [1 ]
Chen, Keyuan [1 ]
Zeng, Xiancheng [1 ]
Yang, Shili [1 ]
Chang, Wei [1 ]
Tang, Yao [3 ]
Chen, Xiaoli [3 ]
Wang, Song [1 ]
Chen, Ji-Long [1 ,2 ]
机构
[1] Fujian Agr & Forestry Univ, Fuzhou 350002, Peoples R China
[2] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
[3] Fuzhou Zoo, Fuzhou 350012, Peoples R China
基金
中国国家自然科学基金;
关键词
Beak and feather disease virus (BFDV); Parrot; FZ strain; Capsid protein (Cap); Phylogenetic analysis; PSITTACINE BEAK; PORCINE CIRCOVIRUS; AVIAN POLYOMAVIRUS; CAPSID PROTEIN; SEQUENCE-ANALYSIS; PARROTS; VACCINATION; PREVALENCE; INFECTION; KINASES;
D O I
10.1007/s12250-019-00159-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Beak and feather disease virus (BFDV) is an infectious agent responsible for feather degeneration and beak deformation in birds. In March 2017, an epidemic of psittacine beak and feather disease (PBFD) struck a farm in Fuzhou in the Fujian Province of southeast China, resulting in the death of 51 parrots. In this study, the disease was diagnosed and the pathogen was identified by PCR and whole genome sequencing. A distinct BFDV strain was identified and named as the FZ strain. This BFDV strain caused severe disease symptoms and pathological changes characteristic of typical PBFD in parrots, for example, loss of feathers and deformities of the beak and claws, and severe pathological changes in multiple organs of the infected birds. Phylogenetic analysis showed that the FZ strain was more closely related to the strain circulating in New Caledonia than the strains previously reported in China. Nucleotide homology between the FZ strain and other 43 strains of BFDV ranged from 80.0% to 92.0%. Blind passage experiment showed that this strain had limited replication capability in SPF Chicken Embryos and DF-1 Cells. Furthermore, the capsid (Cap) gene of this FZ strain was cloned into the pGEX-4T-1 expression vector to prepare the polyclonal anti-Cap antibody. Western blotting analysis using the anti-Cap antibody further confirmed that the diseased parrots were infected with BFDV. In this study, a PBFD and its pathogen was identified for the first time in Fujian Province of China, suggesting that future surveillance of BFDV should be performed.
引用
收藏
页码:43 / 51
页数:9
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