Identification of Beclin-1 from orange-spotted grouper (Epinephelus coioides) involved in viral infection

被引:14
作者
Cai, Jia [1 ,2 ,3 ,4 ]
Zou, Zihong [1 ,2 ,3 ]
Wei, Shina [4 ,5 ]
Zheng, Qi [1 ,2 ,3 ]
Xu, Yongxian [1 ]
Lu, Yishan [1 ,2 ,3 ,4 ]
Wu, Zaohe [2 ,3 ]
Qin, Qiwei [4 ,5 ]
Jian, Jichang [1 ,2 ,3 ,4 ]
机构
[1] Guangdong Ocean Univ, Coll Fishery, Zhanjiang 524088, Peoples R China
[2] Guangdong Prov Key Lab Pathogen Biol & Epidemiol, Zhanjiang 524088, Peoples R China
[3] Guangdong Key Lab Control Dis Aquat Econ Anim, Zhanjiang 524088, Peoples R China
[4] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao, Shandong, Peoples R China
[5] South China Agr Univ, Coll Marine Sci, Guangzhou 510642, Guangdong, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Beclin-1; Orange-spotted grouper; RGNNV; Interferon; Inflammatory; Autophagy; MOLECULAR CHARACTERIZATION; AUTOPHAGY GENES; IMMUNE-RESPONSE; EXPRESSION; PROTEINS; MECHANISMS; FACTOR-3; TRAF6; PCR;
D O I
10.1016/j.fsi.2019.09.029
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Beclin-1 is an essential autophagic regulator that plays diverse roles in physiology and disease. However, reports about the function of fish Beclin-1 during pathogen infection are still very limited. In this study, a Beclin-1 homolog (EcBeclin-1) from orange-spotted grouper (Epinephelus coioides) was identified and its roles in viral infection were investigated. EcBeclin-1 encoded 447amino acids protein with a BH3 domain, a CCD domain and an ECD domain, which shared high identities (97%-82%) with reported Beclin-1 proteins from mammal to fish. Quantitative real-time PCR (qRT-PCR) analysis revealed that EcBeclin-1 was predominantly expressed in brain and muscle of healthy grouper. Using fluorescence microscopy, we found that EcBeclin-1 was co-localized with endoplasmic reticulum (ER) in grouper spleen cells (EAGS). After red-spotted grouper nervous necrosis virus (RGNNV) infection in vitro, EcBeclin-1 transcript was significantly up-regulated, implying that EcBeclin-1 might be involved in viral infection. Furthermore, the in vitro studies of EcBeclin-1 overexpression promoted RGNNV induced autophagy, as well as the expression of coat protein (CP) and RNA-dependent RNA polymerase (RdRp). The overexpression of EcBeclin-1 suppressed the expressions of interferon pathway-related factors, inflammatory-related factors and activities of NF-kappa B and ISRE. Additionally, EcBeclin-1 could interact with EcBcl-xL in vitro. These data suggest that EcBeclin-1 affect viral replication through modulating IFN and inflammatory responses, as well as virus-induced cell death, which will help us to further explore the immune response of fish during viral infection.
引用
收藏
页码:336 / 345
页数:10
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