Recombinant beta interferon could clear the low-dose infected porcine reproductive and respiratory syndrome virus (PRRSV) in MARC-145 cells

被引:9
|
作者
Shi, X. [1 ,3 ]
Zhang, X. [1 ]
Wang, L. [3 ]
Li, W. [1 ]
Jiang, B. [4 ]
Deng, R. [3 ]
Wang, A. [5 ]
Zhang, G. [2 ,3 ]
机构
[1] Henan Normal Univ, Coll Life Sci, Xinxiang 453000, Henan, Peoples R China
[2] Henan Agr Univ, Coll Vet Med & Anim Sci, Zhengzhou 450002, Henan, Peoples R China
[3] Henan Acad Agr Sci, Henan Prov Key Lab Anim Immunol, Key Lab Anim Immunol, Minist Agr, Zhengzhou 450002, Henan, Peoples R China
[4] Chongqing Police Coll, Off Sci & Technol, Chongqing 401331, Peoples R China
[5] Zhengzhou Univ, Dept Bioengn, Zhengzhou 450000, Peoples R China
基金
中国国家自然科学基金;
关键词
PRRSV; recombinant IFN-beta; NONSTRUCTURAL PROTEIN-1; INHIBIT; REPLICATION; IFN; MACROPHAGES; INDUCTION; SYSTEM; ALPHA; GAMMA;
D O I
10.4149/av_2016_03_290
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porcine reproductive and respiratory syndrome virus (PRRSV) causes one of the most economically devastating and pandemic porcine diseases. Previous study has shown that MARC-145 cells pretreated with recombinant IFN-beta (rIFN-beta) couldn't develop cytopathic effect (CPE) of PRRSV. However, up to date, it is not clear whether MARC-145 cells post-treated with rIFN-beta could develop CPE of PRRSV. The present work showed that the MARC-145 cells didn't develop the CPE at 120 hr post-infection (p.i.) with low-dose of PRRSV when the cells were pre-treated with rIFN-beta (Group 1), post-treated with rIFN-beta at 4 hr p.i. (Group 2), or post-treated with rIFN-beta at 8 hr p.i. (Group 3), while the MARC-145 cells could develop CPE when the cells were infected with high-dose PRRSV and then treated with rIFN-beta at 24 hr p.i.. Furthermore, the indirect immunofluorescence assay confirmed that there were a few N protein-positive cells in the high-dose infected cells in Group 1, Group 2 and Group 3, while there were no N protein-positive cells in the low-dose infected. cells in all rIFN-beta treatment groups. In addition, the numbers of N protein-positive cells in high-dose infected cells (MOI = 10) in Group 1 were lower than that in Group 2 and Group 3. The results above demonstrated that both pre-treatment with rIFN-beta and an earlier post-treatment with rIFN-beta could inhibit the PRRSV replication and could clear the low-dose infected PRRSV, which indicated that the rIFN-beta had efficient antiviral activities when the cells have been infected with PRRSV.
引用
收藏
页码:290 / 297
页数:8
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