共 10 条
Circular RNA circAKIRIN2 participates in the process of stress-induced immunosuppression affecting immune response to infectious bursal disease virus vaccine in chicken
被引:2
|作者:
Tian, Yufei
[1
]
Ma, Xiaoli
[1
]
Jiang, Yi
[1
]
Han, Jianwei
[1
]
Zhang, Rui
[1
]
Xu, Xinxin
[1
]
Zhang, Wei
[1
]
Man, Chaolai
[1
,2
]
机构:
[1] Harbin Normal Univ, Coll Life Sci & Technol, Harbin 150001, Peoples R China
[2] 1 Shida Rd Limin Dev Zone, Harbin 150025, Heilongjiang, Peoples R China
关键词:
Chicken;
CircAKIRIN2;
Stress-induced immunosuppression;
IBDV;
ZBTB20;
gene;
CELL-DIFFERENTIATION;
EXPRESSION;
ZBTB20;
GENE;
D O I:
10.1016/j.vetmic.2023.109746
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
At present, stress-induced immunosuppression is still a hidden threat that leads to immunization failure and outbreaks of poultry diseases, and causes huge economic losses to the modern poultry industry. However, the molecular mechanisms of stress-induced immunosuppression affecting viral vaccine immunity are still poorly understood. Here, we identified circAKIRIN2 as a conserved circular transcript in chicken, and explored its expression patterns in different immune states by quantitative real-time PCR (qRT-PCR), then conducted bio-informatics analysis. The results showed that circAKIRIN2 actively participated in the process of stress-induced immunosuppression affecting the immune response to infectious bursal disease virus (IBDV) vaccine. The key time points for circAKIRIN2 involving in the process were 2 day post immunization (dpi), 5 dpi, and 28 dpi, especially at the acquired immune stage. The important tissues that responded to the process included the heart, liver, and lung, all of which changed significantly. In addition, circAKIRIN2 as a competing endogenous RNA (ceRNA) sponging zinc finger and BTB domain containing 20 (ZBTB20) was a potential molecular mechanism for regulating immune functions in the process. In conclusion, circAKIRIN2 is a key regulatory factor for stress-induced immunosuppression affecting the IBDV vaccine immune response, and this study can provide a new perspective for exploring the molecular regulatory mechanisms of stress-induced immunosuppression affecting immune response.
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