Grouper TRADD Mediates Innate Antiviral Immune Responses and Apoptosis Induced by Singapore Grouper Iridovirus (SGIV) Infection

被引:19
作者
Zhang, Xin [1 ]
Liu, Zetian [1 ]
Li, Chen [1 ]
Zhang, Ya [1 ]
Wang, Liqun [1 ]
Wei, Jingguang [1 ,2 ]
Qin, Qiwei [1 ,2 ,3 ]
机构
[1] South China Agr Univ, Joint Lab Guangdong Prov & Hong Kong Reg Marine B, Coll Marine Sci, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Guangdong Prov Key Lab Aquat Econ Anim, Guangzhou, Guangdong, Peoples R China
[3] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao, Shandong, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
grouper; TRADD; SGIV; virus replication; apoptosis; ORANGE-SPOTTED GROUPER; BREAST-CARCINOMA CELLS; DEATH; P53; VIRUS; CYTOTOXICITY; FADD; PHOSPHORYLATION; RECRUITMENT; FILAMENTS;
D O I
10.3389/fcimb.2019.00329
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor necrosis factor (TNF) receptor type 1-associated DEATH domain protein (TRADD) is a TNFR1-associated signal transducer and an essential component of the TNFR1 complex that is involved in activating both apoptotic and nuclear factor (NF)-kappa B pathways as an adaptor. It also is required for TNFR-1-initiated neuronal apoptosis following in vitro infection with virus as an essential component of the antiviral response. To date, few studies have investigated the function of TRADD in lower vertebrates and its antiviral response to DNA virus infection. In the present study, a TRADD gene (named as EcTR4DD) from the orange-spotted grouper (Epinephelus coioides) was cloned and characterized. The full-length cDNA of EcTRADD consists of 1,370 base pairs (bp) and contains a 44 bp 5'-terminal untranslated region (UTR), a 450 bp 3'-UTR including a poly (A) tail, and an 876 bp open reading frame encoding a putative 291 amino acid protein. EcTRADD has two conserved domains of N-terminal domain (TRADD-N) and a death domain (DD). EcTRADD was detected in all examined tissues. EcTRADD was up-regulated in the spleen after infection with Singapore grouper iridovirus (SGIV). Subcellular localization analysis revealed that EcTRADD and EcTRADD-DD exhibited a clear pattern of discrete and interconnecting cytoplasmic filaments resembling the death-effector filaments, while EcTRADD-N was observed in the cytoplasm. After infection with SGIV, EcTRADD, and EcTRADD-DD were transferred to the nucleus. Overexpression of EcTRADD and its domains inhibited replication of SGIV in vitro. Both EcTRADD and EcTRADD-DD induced the caspase-dependent apoptosis in control and infected cells, while EcTRADD-N inhibited the apoptosis. Additionally, EcTRADD and EcTRADD-DD significantly promoted activation of NF-kappa B and reporter gene p53, whereas EcTRADD-N had no significant effect on p53. The results may provide new insights into the role of fish TRADD in fish virus infection.
引用
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页数:14
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共 48 条
[1]   Adenovirus-mediated transfer of wild-type p53 gene sensitizes TNF resistant MCF7 derivatives to the cytotoxic effect of this cytokine:: relationship with c-myc and Rb [J].
Ameyar, M ;
Shatrov, V ;
Bouquet, C ;
Capoulade, C ;
Cai, ZZ ;
Stancou, R ;
Badie, C ;
Haddada, H ;
Chouaib, S .
ONCOGENE, 1999, 18 (39) :5464-5472
[2]   Resistance of MCF7 human breast carcinoma cells to TNF-induced cell death is associated with loss of p53 function [J].
Cai, ZZ ;
Capoulade, C ;
MoyretLalle, C ;
AmorGueret, M ;
Feunteun, J ;
Larsen, AK ;
BressacdePaillerets, B ;
Chouaib, S .
ONCOGENE, 1997, 15 (23) :2817-2826
[3]   Selenocystine induces caspase-independent apoptosis in MCF-7 human breast carcinoma cells with involvement of p53 phosphorylation and reactive oxygen species generation [J].
Chen, Tianfeng ;
Wong, Yum-Shing .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2009, 41 (03) :666-676
[4]   Apoptosis in animal models of virus-induced disease [J].
Clarke, Penny ;
Tyler, Kenneth L. .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (02) :144-155
[5]   Phosphorylation of the tumor necrosis factor receptor CD120a (p55) recruits Bcl-2 and protects against apoptosis [J].
Cottin, V ;
Van Linden, AA ;
Riches, DWH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) :17252-17260
[6]   Homeodomain-interacting protein kinase-2 phosphorylates p53 at Ser 46 and mediates apoptosis [J].
D'Orazi, G ;
Cecchinelli, B ;
Bruno, T ;
Manni, I ;
Higashimoto, Y ;
Saito, S ;
Gostissa, M ;
Coen, S ;
Marchetti, A ;
Del Sal, G ;
Piaggio, G ;
Fanciulli, M ;
Appella, E ;
Soddu, S .
NATURE CELL BIOLOGY, 2002, 4 (01) :11-19
[7]   Regulation of p53 activity in nuclear bodies by a specific PML isoform [J].
Fogal, V ;
Gostissa, M ;
Sandy, P ;
Zacchi, P ;
Sternsdorf, T ;
Jensen, K ;
Pandolfi, PP ;
Will, H ;
Schneider, C ;
Del Sal, G .
EMBO JOURNAL, 2000, 19 (22) :6185-6195
[8]   EVER2 protein binds TRADD to promote TNF-α-induced apoptosis [J].
Gaud, G. ;
Guillemot, D. ;
Jacob, Y. ;
Favre, M. ;
Vuillier, F. .
CELL DEATH & DISEASE, 2013, 4 :e499-e499
[9]   A PERMANENT CELL LINE FROM FATHEAD MINNOW (PIMEPHALES PROMELAS) [J].
GRAVELL, M ;
MALSBERGER, RG .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1965, 126 (A1) :555-+
[10]   Caspase recruitment domain (CARD)-dependent cytoplasmic filaments mediate bcl10-induced NF-κB activation [J].
Guiet, C ;
Vito, P .
JOURNAL OF CELL BIOLOGY, 2000, 148 (06) :1131-1139