Isolation and pathogenicity of porcine circovirus type 2 in mice from Guangxi province, China

被引:1
|
作者
Jiao, Qiulin [1 ,2 ]
Yang, Liuyue [1 ,2 ]
Liu, Xiangzu [1 ,2 ]
Wen, Yanwen [1 ,2 ]
Tian, Linxing [1 ,2 ]
Qian, Ping [1 ,2 ,3 ]
Chen, Huanchun [1 ,2 ,3 ]
Li, Xiangmin [1 ,2 ,3 ]
机构
[1] Huazhong Agr Univ, Natl Key Lab Agr Microbiol, Hubei Hongshan Lab, Wuhan 430070, Hubei, Peoples R China
[2] Huazhong Agr Univ, Coll Vet Med, Wuhan 430070, Hubei, Peoples R China
[3] Cooperat Innovat Ctr Sustainable Pig Prod, Key Lab Prevent Vet Med Hubei Prov, Wuhan 430070, Hubei, Peoples R China
关键词
Porcine circovirus type 2; Isolation; Phylogenetic analysis; Pathogenicity; MULTISYSTEMIC WASTING SYNDROME; NEPHROPATHY SYNDROME; PHYLOGENETIC ANALYSIS; CAPSID PROTEIN; SYNDROME PMWS; PCV2; INFECTION; PIGS; DERMATITIS; IDENTIFICATION;
D O I
10.1186/s12985-023-02161-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BackgroundPorcine circovirus type 2 (PCV2), a member of the genus Circovirus and family Circoviridae, is a closed, small, circular, and single-stranded DNA virus, and it is a crucial swine pathogen of porcine circovirus-associated diseases (PCVADs). PCV2 was first detected in PK-15(ATCC-CCL) cells in 1974, which has caused significant economic loss to the swine industry throughout the world. And the first case of PCV2 was reported in China in 2000. At present, PCV2d is the main genotype circulating widely in China.MethodsLymph samples were obtained from piglets with emaciation and respiratory disease in Guangxi province, China. The main pathogens were detected via PCR from lymph samples, and then PCV2-single positive samples were used to inoculate with PK-15 cells. After successive generations, the isolate was subsequently identified by polymerase chain reaction (PCR), immunofluorescence assay (IFA), Western blot (WB), and transmission electron microscopic (TEM). The full-length genome and genetic characterization of isolates were analyzed by Sanger sequencing. The TCID50 of the PCV2-GX-6 was determined by IFA, and the pathogenicity of PCV2 in BALB/c mice was analyzed via the mouse model.ResultsThe isolates were successfully isolated from clinical samples. The complete genome of PCV2-GX-4, PCV2-GX-6, PCV2-GX-7, PCV2-GX-11 and PCV2-GX-16 have been amplified, sequenced, and deposited in GenBank (accession no.: OR133747, OQ803314, OR133748, OR133749, OR133750). Homology and phylogenetic analysis with reference strains showed that the isolates belonged to the PCV2d genotype. The PCV2-GX-6 could be stably passaged more than 30 times in PK-15 cells. PCV2-GX-6 was identified by PCR, IFA, WB and TEM. The results of homology showed that PCV2-GX-6 was closely related to the reference strains PCV2-JS17-8 (GenBank accession no.: MH211363). Pathogenicity studies in mice have shown that PCV2-GX-6 can lead to growth inhibition of mice. Meanwhile PCV2-GX-6 caused the typical lesions of spleen, lung and kidney. The results of qPCR showed that PCV2 can effectively proliferate in the liver, spleen, lung, and kidney.ConclusionPCV2-GX-6 can successfully infect BLAB/c mice, effectively proliferate in major organs, and possessed high pathogenicity. In conclusion, combined with the genotype and pathogenicity of PCV2d currently prevalent, PCV2-GX-6 can be used as a candidate vaccine strain.
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