Stress-induced immunosuppression inhibits immune response to infectious bursal disease virus vaccine partially by miR-27b-3p/SOCS3 regulatory gene network in chicken

被引:4
|
作者
Ma, Xiaoli [1 ]
Tian, Yufei [1 ]
Zhang, Wei [1 ]
Zhang, Rui [1 ]
Xu, Xinxin [1 ]
Han, Jianwei [1 ]
Jiang, Yi [1 ]
Wang, Xiangnan [1 ]
Man, Chaolai [1 ]
机构
[1] Harbin Normal Univ, Coll Life Sci & Technol, Harbin 150001, Peoples R China
关键词
SOCS3; gene; miR-27b-3p; stress-induced immunosuppression; infectious bursal disease virus; immune response; SOCS PROTEINS; CELLS; PATHWAYS;
D O I
10.1016/j.psj.2023.103164
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Stress-induced immunosuppression (SIIS) is one of the common problems in intensive poultry production, which often reduces the prevention and control effects of various vaccines, including infectious bursal disease virus (IBDV) vaccine, and brings enormous economic losses to the poultry industry. However, the molecular mechanisms of SIIS inhibiting immune response to IBDV vaccine remain unclear. In this study, suppressor of cytokine signaling 3 (SOCS3) gene was selected and stress-induced immunosuppressed chickens were simulated using dexamethasone (Dex). Quantitative real-time PCR (qRT-PCR) was conducted to analyze its expression characteristics and game relationships between SOCS3 gene and miR-27b-3p (it could target SOCS3 gene) in the process of SIIS inhibiting immune response to IBDV vaccine in chicken, and the potential application value of circulating miR-27b-3p as a biomarker was also identified. The results showed that SOCS3 gene and miR-27b-3p were significantly differentially expressed in the candidate tissues during SIIS inhibiting the immune response to IBDV (P < 0.05), respectively, which were key factors involved in the process. Moreover, miR-27b-3p and SOCS3 gene showed game regulation relationships in several tissues during the process, so the miR-27b-3p/SOCS3 regulatory network was one of the key mechanisms of SOCS3 gene participating in the process. Circulating miR-27b-3p was differentially expressed in serum at 10 time points (1, 2, 3, 4, 5, 7, 14, 21, 28, and 35 days postimmunization (dpi)) in the process (P < 0.05), showing that circulating miR-27b-3p was a valid candidate target as a molecular marker for detecting SIIS inhibiting the IBDV immune response. This study can provide references for further studying molecular mechanisms of stress affecting immune response.
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页数:10
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