Original Research ARTICLE
Functional Characterization of Dark Sleeper (Odontobutis obscura) TBK1 on IFN Regulation
- 1Fisheries Research Institute, Wuhan Academy of Agricultural Sciences, Wuhan, China
- 2State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China
- 3University of Chinese Academy of Sciences, Beijing, China
- 4Key Laboratory of Aquaculture Disease Control, Ministry of Agriculture, Wuhan, China
In East Asia, the dark sleeper, Odontobutis obscura (O. obscura) is a crucial commercial species of freshwater fish; however, its molecular biology research is still undeveloped, including its innate immune system, which is pivotal to antiviral responses. In this study, we cloned and identified the characterization and kinase function of dark sleeper TANK-binding kinase 1 (TBK1), supplementing the evidence of the conservation of this classical factor in fish. First, the ORF of Odontobutis obscurus (O. obscura) TBK1 (OdTBK1) was cloned from liver tissue by RACE-PCR. Subsequent nucleic acid and amino acid sequence analysis suggested that OdTBK1 is homologous with other fish TBK1, and the N-terminal Serine/Threonine protein kinases catalytic domain (S_TKc) and C-terminal coiled coil domain (CCD) are conserved. Subsequently, the cellular distribution demonstrated that OdTBK1 was located in the cytoplasm region. With regard to the identification of functions, OdTBK1 activated several interferon (IFN) promoters' activity and induced downstream IFN-stimulated genes (ISGs) expression. In a canonical manner, wild-type OdTBK1 significantly phosphorylated interferon regulatory factor 3 (IRF3) but failed when the N-terminal region was truncated. Furthermore, overexpression of OdTBK1 decreased viral proliferation remarkably. Collectively, these data systematically analyzed the characterization and function of OdTBK1, initiating the study of the innate antiviral response of dark sleeper.
- OdTBK1 promotes fish IFNs transcription.
- OdTBK1 phosphorylates IRF3 as a kinase.
- OdTBK1 exhibits a powerful antiviral capacity.
A variety of pattern recognition receptors (PRRs) mediate a host's innate immune response to pathogen invasion; six families have been identified, including Toll-like receptors (TLRs), C-type lectins (CTLs), NOD-like receptors (NLRs), RIG-I-like receptors (RLRs), AIM2-like receptors (ALRs), and OAS-like receptors (OLRs). Among them, RLRs are cytoplasmic sensors of RNA (1). Upon activation, they signal to the mitochondrial antiviral signaling protein (MAVS, also called IPS-1, Cardif, or VISA) (2–4) to form active MAVS polymers and subsequently recruit tumor necrosis factor (TNF) receptor-associated factor (TRAF) family ubiquitin E3 ligases to synthesize polyubiquitin chains, which activates IKK and TANK-binding kinase 1 (TBK1). The recruited kinases then phosphorylate MAVS at its conserved pLxIS motif, and, at the same time, the potential transcription factors interferon regulatory factor (IRF) 3 and IRF7 are phosphorylated by IκB kinase IKKε or TBK1. Thereafter, phosphorylated IRF3 and IRF7 form dimers that accumulate in the nuclei where they bind to target sequences to activate the IFN-β promoter to initiate interferon (IFN) secretion (5).
TBK1 contains an N-terminal kinase, an ubiquitin like domain and two C-terminal coiled-coil domains (6). Recruiting of multiple TBK1 dimers to signaling complexes enables activation-loop swapping of locally clustered TBK1 and results in TBK1 auto-phosphorylation (7). In addition, TBK1 is a serine/threonine protein kinase of the IKK kinase family involved in innate immunity to viral infection by inducing type I IFNs and mediating TANK's ability to activate NF-κB (6, 8).
Upon stimulation by virus structural components, pattern recognition receptors (PRRs) recruit TLR/IL-1R domain-containing adaptor proteins, inducing IFN-β (TRIF), MAVS, and a stimulator of IFN genes (STING; also called MITA, MPYS, and ERIS) to activate TBK1 (9–11). Activated TBK1 phosphorylates IRF3/7, triggers dimerization and nuclear translocation, and leads to formation of active transcriptional complexes that bind to IFN stimulation response elements (ISRE), activating type I IFN gene expression (12). Knockdown assays and gene-targeting studies have shown that TBK1 is essential for type I IFN production in TLR3 and RLR signaling pathways (13–15).
TBK1 has been identified in a variety of fishes. The TBK1 of black carp (Mylopharyngodon piceus), named bcTBK1, shows antiviral activity against both Grass Carp Reovirus (GCRV) and Spring Viremia of Carp Virus (SVCV) (16). TBK1 in the large yellow croaker (Larimichthys crocea) (named LcTBK1) can interact with an E3 ubiquitin ligase LcNrdp1 to defend against Cryptocaryon irritans infection (17). Upon LPS stimulation, TBK1 from grass carp (Ctenopharyngodon idella) (CiTBK1) triggers IFN response in an IRF3/IRF7-independent manner (18). In addition, Danio rerio TBK1 (DrTBK1) or Carassius auratus TBK1 (CaTBK1) can cause the phosphorylation of IRF3/7 (19, 20). Nevertheless, in teleost fish, the identification of the molecular characteristics and mechanisms of TBK1 are still limited.
The dark sleeper (Odontobutis obscurus), an important commercial fish species, is widely distributed in the river systems of southeast China (21, 22). In recent years, because of its delicious taste and high nutritional value, the dark sleeper has become a very promising aquaculture species in China. However, some viruses seriously threaten its growth. Better understanding of antiviral immune mechanisms may contribute to the development of management strategies for disease control.
In this study, we report the characterization of Odontobutis obscurus (O. obscura) TBK1 (OdTBK1). Our findings demonstrate that OdTBK1 is effective for zebrafish and grass carp IFN promoters and significantly induces IFN-stimulated gene (ISG) expression. It can also promote the phosphorylation of IRF3 both in Danio rerio (D. rerio) and O. obscura. OdTBK1 plays a critical role in the antiviral immune defense of fish in promoting the IFN response.
Materials and Methods
Cells and Viruses
Epithelioma papulosum cyprinid (EPC, now IDed as fathead minnow) and Grass carp ovary (GCO) cells were maintained at 28°C, 5% CO2 in medium 199 (Invitrogen) supplemented with 15% fetal bovine serum (FBS, Invitrogen) (23). Human embryonic kidney (HEK) 293T cells were grown at 37°C, 5% CO2 in DMEM medium (Invitrogen) supplemented with 15% FBS. Spring Viremia of Carp Virus (SVCV-741, 109 TCID50/ml), a negative-sense ssRNA virus, was propagated in EPC cells until cytopathic effect (CPE) were observed, then the cultured media with cells was harvested and stored at −80°C until use.
Healthy dark sleeper (weighing 40 ± 20 g) purchased from a fish farm were maintained and acclimated to re-circulating tanks (1,000-L, 28 ± 1°C) containing filtered and oxygenated water for at least 2 weeks before experiments. All animal experiments were approved by the Committee on the Ethics of Animal Experiments of the Chinese Academy of Sciences.
Amplification of OdTBK1 and Plasmid Construction
Rapid amplification of cDNA ends (RACE) was carried out using the 5′ RACE system (Invitrogen) and BD SMARTTM RACE cDNA amplification kit (BD Biosciences Clontech) according to the manufacturer's instruction. The first strand cDNA synthesis and RACE were performed on liver-derived RNA. To obtain the 3′ unknown region, primer pairs OdTBK1F4a/APT and OdTBK1F5a/AP (Table 1), were used for the primary PCR and the nested PCR, respectively. The amplified PCR product was cloned and sequenced as described above. Similarly, the 5′ end of OdTBK1 was obtained by nested PCR using primer pairs OdTBK1R2a/APG and OdTBK1R3a/AP (Table 1). The full-length cDNA sequence was confirmed by sequencing the PCR product amplified by primers OdTBK1-FP and OdTBK1-RP (Table 1) within the predicted 5′ and 3′ untranslated regions, respectively. The open reading frame (ORF) of OdTBK1 was subcloned into pcDNA3.1(+) (Invitrogen), pCMV-Myc (Clontech) and pCMV-Tag2C (Clontech), respectively. For subcellular localization, the ORF of OdTBK1 was inserted into pEGFP-N3 (Clontech) vector. The ORFs of zebrafish IRF3 (NM_001143904) was subcloned into pCMV-HA (Clontech) and pCMV-Myc vector. The primers used to amplify the N-terminal absent OdTBK1 sequence were OdTBK1-ΔN-FP and OdTBK1-RP (Table 1). It was also subcloned into pCMV-Tag2C and pCMV-Myc vector. The fmIFN promoter was obtained from NCBI database (HE856618.1) and cloned into pGL3-Basic luciferase reporter vector (Promega). The plasmids containing DrIFNϕ1pro-Luc, DrIFNϕ3pro-Luc, gcIFN1, and ISRE-Luc in pGL3-Basic luciferase reporter vectors were constructed as described previously (24, 25). All constructs were confirmed by DNA sequencing.
The phylogenetic tree was constructed with the Neighbor-joining method (NJ) by MEGA7 program which was bootstrapped 500 times. All gene sequences used in this study were derived from GenBank. Multiple alignments were accomplished using GENE.DOC.
Transient Transfection and Virus Infection
Transient transfections were performed in EPC cells or GCO cells seeded in 6-well or 24-well plates by using X-tremeGENE HP DNA Transfection Reagent (Roche) according to the manufacturer's protocol. And the transfection efficiency of EPC cells or GCO cells is nearly 50%. To confirm the antiviral response of OdTBK1, EPC cells were seeded in 24-well plates overnight and transfected with 0.5 μg OdTBK1-Myc or the pCMV-Myc vector separately. At 24 h post-transfection, the EPC cells were infected with SVCV at a multiplicity of infection (MOI = 0.01) and incubated at 28°C. The supernatant aliquots were then harvested to detect the virus titers at 48 h post infection, using the standard 50% tissue culture infection dose (TCID50) method. The cell monolayers were washed with PBS, fixed with 4% paraformaldehyde (PFA) for 1 h, and stained with 0.05% crystal violet overnight, and observed for the cytopathic effect (CPE). For virus titration, 200 μl of culture medium were collected at 48 h post-infection, and used for plaque assay. The supernatants were subjected to 3-fold serial dilutions and then added (100 μl) onto a monolayer of EPC cells cultured in a 96-well plate. After 48 or 72 h, the medium was removed and the cells were washed with PBS, fixed by 4% PFA and stained with 1% crystal violet. The virus titer was expressed as 50% tissue culture infective dose (TCID50/ml). Results are representative of three independent experiments.
Luciferase Activity Assay
EPC cells were seeded in 24-well plates, and 24 h later co-transfected with 250 ng luciferase reporter plasmid (DrIFNϕ1pro-Luc, DrIFNϕ3pro-Luc, ISRE-Luc, or fmIFN-Luc) and 250 ng OdTBK1-Myc or pCMV-Myc and 50 ng Renilla luciferase internal control vector (pRL-TK, Promega). Empty vector pCMV-Myc was used to maintain equivalent amounts of DNA in each well. GCO cells were used to detect ISRE-Luc and gcIFN1-Luc. At 24 h post-transfection, the cells were washed in PBS and lysed for measuring luciferase activity by Dual-Luciferase Reporter Assay System, according to the manufacturer's instructions (Promega). Firefly luciferase activities were normalized on the basis of Renilla luciferase activity. The results were representative of more than three independent experiments, each performed in triplicate.
EPC cells were plated onto coverslips in 6-well plates and transfected with indicated plasmids for 24 h. The experimental group was stimulated with the viral analog polyinosinic-polycytidylic acid (poly I:C) 12 h before the photo was taken. Then the cells were washed twice with PBS and fixed with 4% PFA for 1 h. After draining the fixative, the cells were stained with DAPI (C1006, Beyotime) for 5 min in dark at room temperature. Finally, the coverslips were washed and observed with a Leica confocal microscope under a × 63 oil immersion objective (SP8; Leica Microsystems).
RNA Extraction, Reverse Transcription, and Quantitative Real-Time PCR
The total RNA from brain, pituitarium, eye, gill, heart, liver, muscle, spleen, head kidney, and ovary were extracted from three apparently healthy dark sleepers to detect the expression of OdTBK1.
Total RNAs of EPC cells and tissues were extracted by Trizol reagent (Invitrogen). RNase-free DNase is used specifically for RNA purification by removing all contaminating genomic DNA. The first-strand cDNA was synthesized by using a GoScript Reverse Transcription System (Promega) according to the manufacturer's instructions. Quantitative real-time PCR (qPCR) was performed with Fast SYBR Green master mix (BioRad) on a CFX96 Real-Time System (BioRad). PCR conditions were as follows: 95°C for 5 min, then 40 cycles of 95°C for 20 s, 60°C for 20 s, 72°C for 20 s. and the β-actin primers were used as internal control. The specificity of the PCR amplification for all primer sets was verified from the dissociation curves. The identity of each PCR products was confirmed by dideoxy-mediated chain termination sequencing at Wuhan TSINGKE Biological Technology Inc. The relative fold changes were calculated by comparison to the corresponding controls using the 2−ΔΔCt method. Three independent experiments were conducted for statistical analysis. The total RNA extracted from the tissue of liver also treated as cells.
For transient-transfection and Co-IP experiments, HEK 293T cells were used instead of EPC cells due to the superhigh transfection efficiency of HEK 293T cells. Cells seeded into 10-cm2 dishes overnight were transfected with a total of 10 μg the indicated plasmids. At 24 h post transfection, the medium was removed carefully, and the cell monolayer was washed twice with 10 ml ice-cold phosphate-buffered saline (PBS). The cells were then lysed in 1.0 ml radioimmunoprecipitation (RIPA) lysis buffer (1% NP-40, 50 mM Tris-HCl [pH 7.5], 150 mM NaCl, 1 mM EDTA, 1 mM NaF, 1 mM sodium orthovanadate [Na3VO4], 1 mM phenylmethylsulfonyl fluoride [PMSF], 0.25% sodium deoxycholate) containing a protease inhibitor cocktail (Sigma-Aldrich) at 4°C for 1 h on a rocker platform. The cellular debris was removed by centrifugation at 12,000 × g for 15 min at 4°C. The supernatant was transferred to a fresh tube and incubated with 20 μl anti-Flag affinity gel (Sigma-Aldrich) overnight at 4°C with constant agitation. These samples were further analyzed by Immunoblotting (IB). Immunoprecipitated proteins were collected by centrifugation at 5,000 × g for 1 min at 4°C, washed three times with lysis buffer, and resuspended in 100 μl 5 × SDS sample buffer. The immunoprecipitates and whole-cell lysates were analyzed by IB with the indicated Abs.
In vitro Protein Dephosphorylation Assay
Transfected HEK 293T cells were lysed as described above, except that the phosphatase inhibitors (Na3VO4 and EDTA) were omitted from the lysis buffer. Protein dephosphorylation was carried out in 100 μl reaction mixtures consisting of 100 μg of cell protein and 10 U of CIP (Sigma-Aldrich). The reaction mixtures were incubated at 37°C for 1 h, followed by Western blotting analysis.
Whole cells were lysed in radioimmunoprecipitation (RIPA) lysis buffer [1% NP-40, 50 mM Tris-HCl (pH 7.5), 150 mM NaCl, 1 mM EDTA, 1 mM NaF, 1 mM sodium orthovanadate, 1 mM phenyl-methylsulfonyl fluoride, and 0.25% sodium deoxycholate] containing protease inhibitor mixture (Sigma-Aldrich). The Bradford method was used for estimation of protein concentration of cell lysates. The equivalent amount of proteins (10 μg) in different groups were separated by 10% SDS-PAGE and transferred to PVDF membrane (Bio-Rad). The membranes were blocked for 1 h at room temperature in TBST buffer (25 mM Tris-HCl, 150 mM NaCl, 0.1% Tween-20, pH 7.5) containing 5% nonfat dry milk, probed with indicated primary antibodies (Abs) at an appropriate dilution overnight at 4°C, washed three times with TBST and then incubated with secondary Abs for 1 h at room temperature. After additional three washes with TBST, the membranes were stained with Immobilon TM Western Chemiluminescent HRP Substrate (Millipore) and detected using an Image Quant LAS4000 system (GE Healthcare). Abs were diluted as follows: anti-Myc (Santa Cruz Biotechnology) at 1:2000, HRP-conjugated anti-mouse IgG (Thermo Scientific) at 1:5000. The results were the representative of three independent experiments.
The results are expressed as mean ± SEM. Data were analyzed using a Student's unpaired t-tests. A p < 0.05 was considered to be statistically significant.
Molecular Cloning and Phylogenetic Analysis of OdTBK1
The coding sequence (CDS) of OdTBK1 was obtained by RACE-PCR. The full-length ORF of OdTBK1 is 2,172 bp, encoding 723 amino acids through initial sequence analysis of OdTBK1 prediction. The SMART program predicted that there were Serine/Threonine protein kinases catalytic domain (S_TKc) in N terminus (9-306) and coiled coil domain (CCD) in C terminus (678-704). To investigate the homology of OdTBK1, phylogenetic analyses of TBK1 with several species were conducted by MEGA7 based on the CDS sequences; these members could be divided into mammals, amphibians, mollusks, and fish (Figure 1). OdTBK1 showed high homology with the TBK1 of L. crocea. Additionally, OdTBK1 and the TBK1 homologs of D. rerio and G. morhua shared similar positions on the homology. Meanwhile, multiple alignments of OdTBK1 to the corresponding sequences of other species showed that the N-terminal kinases catalytic domains of TBK from the teleost were conserved (Figure 2).
Figure 1. Phylogenetic tree of various TBK1 members. The tree was depicted on the overall sequences by neighbor-joining method. The 0.1 scale indicates the genetic distance. Accession numbers of TBK1 amino acid sequences are as follows: Odontobutis obscura (dark sleeper), MK637832; Oplegnathus fasciatus (Stone bream), AHX37216.1; Paralichthys olivaceus (bastard halibut), AGL54166.1; Larimichthys crocea (large yellow croaker), AKM77645.1; Salmo salar (Atlantic salmon), AEA42006.1; Gadus morhua (Atlantic cod), ADL60136.1; Danio rerio (zebra fish), NP_001038213.2; Cyprinus carpio (koi), ADZ55455.1; Xenopus tropicalis (Western clawed frog), NP_001135652.1; Crassostrea gigas (Thunberg), APX43288.1; Cuculus canorus (Cuckoo), XP_009554581.1; Mus musculus (Mouse), AAF05990.1; Sus scrofa (Pig), NP_001098762.1; Bos taurus (Bovine), NP_001179684.1; Homo sapiens (Human), AAF05989.1.
Figure 2. Sequence alignment of the amino acid sequence of TBK1 from several species was carried out by Gene Doc. Conserved N-terminal Serine/Threonine protein kinases catalytic domain (S_TKc) was showed in the black box, C-terminal coiled coil domain (CCD) was showed in the gray box.
Tissue-Specific Expression Pattern of OdTBK1
To investigate the mRNA level of OdTBK1 in vivo, total RNA was isolated from brain, pituitarium, eye, gill, heart, liver, muscle, spleen, kidney, and ovary of the black sleeper separately. The tissue distribution pattern of OdTBK1 was monitored by qRT-PCR. Transcripts of OdTBK1 were detected in all ten tissues: the highest level of OdTBK1 was observed in pituitarium, while the lowest level of OdTBK1 appeared in the head kidney. Generally, the expression levels of OdTBK1 were basically the same across tissues (Figure 3). These data demonstrated that OdTBK1 was ubiquitously expressed in the tissues of the dark sleeper.
Figure 3. Expression analysis of OdTBK1 in different tissues. Total RNAs of various tissues in dark sleeper were extracted to examine the transcripts of OdTBK1, β-actin was used as an internal control for normalization to give relative expression. The expression levels in the other tissues are shown as fold induction compared with the head kidney (for which their relative expressions were set to 1). Error bars represents the means ± SEM (n = 3), and the experiments were repeated three time with similar results.
OdTBK1-Mediated IFNs and ISRE Activation
TBK1 is a crucial factor involved in type I IFN response. To clarify whether OdTBK1 activates IFN production, the luciferase report gene assay was employed in the following manner. Co-transfection of the OdTBK1 and IFN promoters occurred in EPC cells, and the activities of these promoters were measured 24 h later. According to the results, OdTBK1 significantly upregulated the activation of the DrIFNϕ1 promoter up to 7.6-fold compared with the empty vector control group (Figure 4A). Similarly, the activation of the DrIFNϕ3 promoter increased by 6.3-fold compared with the control group (Figure 4B). The activation of the fmIFN promoter was also measured, and it was significantly induced about 20-fold compared with the empty vector control group (Figure 4C). Then, ISRE was co-transfected with OdTBK1 in GCO cells to monitor the capacity of OdTBK1 in another fish cell line. Consistent with the result above, ISRE was significantly enhanced 24-fold by OdTBK1 overexpression (Figure 4D). Finally, GcIFN1 was co-transfected with OdTBK1 in the same way, and its activity was also upregulated about 16-fold (Figure 4E). These results demonstrated that OdTBK1 conservatively activated the IFN promoters from different fishes.
Figure 4. (A–E) Activation of DrIFNϕ1, DrIFNϕ3 and ISRE promoters by overexpression of OdTBK1. EPC cells were seeded on 24-well-plates overnight and co-transfected with pCMV-Myc or OdTBK1-Myc and DrIFNϕ1pro-Luc (A), DrIFNϕ3pro-Luc (B), fmIFNpro-Luc (C). GCO cells were treated at the same way and co-transfected with pCMV-Myc or OdTBK1-Myc and gcIFN1pro-Luc (D), ISRE-Luc (E). The luciferase assays were performed 24 h after transfection. The promoter activity is presented as relative light units normalized to Renilla luciferase activity. Error bars represents the means ± SEM (n = 3), and the experiments were repeated three time with similar results. Asterisks indicate significant differences from control (*p < 0.05).
Cytoplasm Localization of OdTBK1
Fluorescence microscopy was used to investigate the subcellular localization of OdTBK1 with or without I:C stimulation or SVCV infection. Poly I:C, an RNA virus mimic, can induce IFN expression significantly. EPC cells transfected with EGFP-N3 were used as a control group. The fluorescent signals of EGFP-N3 were distributed in the cytosol and the nucleus with or without poly I:C stimulation or SVCV infection. Compared with the controls, without stimulation, the green signals of OdTBK1 were detected in the cytosol, with none in the nucleus. After poly I:C stimulation or SVCV infection, green fluorescent signals were also detected only in the cytosol (Figure 5). These data suggested that OdTBK1 was localized in the cytoplasm.
Figure 5. Subcellular localization of OdTBK1. EPC cells seeded onto microscopy cover glass in 6-well plates were transfected with 2 μg EGFP-OdTBK1 or the empty vector. After 24 h, the cells were untreated (null) or transfected with 2 μg poly (I:C) or infected with 4 μl SVCV for 12 h, then the cells were fixed and subjected to confocal microscopy analysis. Green staining represents the OdTBK1 protein signal, and blue staining indicates the nucleus region (original magnification, ×63; oil immersion objective). Bar, 10 μm. All experiments were repeated at least three times, with similar results.
OdTBK1 Acted as a Kinase to Phosphorylate IRF3
As mentioned earlier, IRF3 is a crucial downstream signaling molecule of TBK1. After co-transfection of zebrafish IRF3 (DrIRF3) and OdTBK1, cells were lysed for immunoblotting. Compared with the signal band of DrIRF3 in the control group, band shifts occurred through stimulation with OdTBK1 (Figure 6A). To confirm whether the shifted bands represented phosphorylated IRF3, a dephosphorylation assay was performed in vitro. The shifted bands partially disappeared after being treated with calf intestinal phosphatase (CIP), demonstrating that DrIRF3 can be phosphorylated by OdTBK1 (Figure 6B). To further characterize this process, a truncated OdTBK1 mutant was generated to identify the functional domain that regulates the phosphorylation of DrIRF3. As shown in Figure 6C, the mutant lacking the kinase domain (OdTBK1-ΔN) failed to phosphorylate DrIRF3, suggesting that this domain was indispensable for its kinase activity (Figure 6C). In addition, to validate the association between OdTBK1 and DrIRF3, we transfected expression plasmids for DrIRF3-Myc and OdTBK1-Flag into HEK 293T cells and performed Co-IP assays. The results indicate that OdTBK1 interacted with DrIRF3 (Figure 6D) and was involved in phosphorylation of DrIRF3 via its functional kinase domain.
Figure 6. IRF3 was phosphorylated by OdTBK1. (A) Overexpression of OdTBK1 induces the phosphorylation of DrIRF3 in a dose-dependent manner. HEK 293T cells were seeded in six-well plates overnight and co-transfected with 1 μg DrIRF3-HA (attachment of a HA tag to the N terminus of DrIRF3) and 1 μg empty vector, or OdTBK1-Myc (0.25, 0.5 and 1 μg, respectively) for 24 h. The cell lysates were subjected to IB with the anti-HA, anti-Myc, and anti-β-actin Abs. (B) OdTBK1 mediates the phosphorylation of DrIRF3. HEK 293T cells were seeded in six-well plates overnight and co-transfected with 1 μg DrIRF3-HA and 1 μg empty vector or OdTBK1-Myc for 24 h. The cell lysates (100 μg) were treated with or without CIP (10 U) for 40 min at 37°C. The lysates were then subjected to IB with the anti-HA, anti-Myc, and anti-β-actin Abs. (C) IRF3 was phosphorylated by the N terminus of OdTBK1. HEK 293T cells were seeded in six-well plates overnight and transfected with the indicated plasmids (1 μg each) for 24 h. The cell lysates were subjected to IB with the anti-Myc and anti-β-actin Abs. (D) OdTBK1 associates with DrIRF3. HEK 293T cells seeded into 10-cm2 dishes were transfected with the indicated plasmids (10 μg each). After 24 h, cell lysates were immunoprecipitated (IP) with anti-Flag affinity gel. The immunoprecipitates and cell lysates were then analyzed by IB with anti-Myc and anti-Flag Abs, respectively. All experiments were repeated at least three times with similar results.
OdTBK1 Induced Downstream ISGs Expression
OdTBK1 significantly phosphorylates IRF3, which is a crucial transcriptional factor of IFN, to activate ISGs expression. Therefore, the regulation activity of OdTBK1 was monitored. EPC cells were transfected with OdTBK1 and total RNA was extracted for reverse transcription. qRT-PCR was employed to detect several genes involved in IFN-mediated pathways, such as ifn, mavs, and vig1 (26). The transcription levels of these ISGs increased significantly compared with the control group. The mRNA level of ifn was increased by 61-fold compared with the control group, and that of vig1 was increased by 15-fold (Figures 7A–C). These data indicated that OdTBK1 was capable of activating ISG transcription.
Figure 7. Overexpression of OdTBK1 induces the expressions of ISGs in EPC cells. (A–C) qPCR detection of the transcript levels of ISGs in OdTBK1-overexpressing cells. EPC cells seeded in 6-well plates overnight were transfected with 1.5μg OdIRF3-Myc or empty vector for 24 h. Then total RNAs were extracted to examine the transcripts of ifn (A), mavs (B), and vig1 (C) by qPCR. β-actin was used as an internal control for normalization and the relative expression is represented as fold induction relative to the expression level in control cells (set to 1). Error bars represents the means ± SEM (n = 3), and the experiments were repeated three time with similar results. Asterisks indicate significant differences from control (*p < 0.05).
Antiviral Activity of OdTBK1
Finally, to investigate the role of OdTBK1 in host antiviral immunity, EPC cells were transfected with OdTBK1 and the pCMV-Myc group was used as a control group. These two groups were separately infected with identical titers of SVCV at 24 h post-transfection. At 36 h after the infection, apparent CPE was observed in the control cells, while the CPE of the OdTBK1 group was obviously reduced (Figure 8A). Measurement of the virus titers of the OdTBK1 and control groups suggested that it was reduced over 30-fold in the OdTBK1-overexpressing cells compared with the control cells (Figure 8B). The data above demonstrated that OdTBK1 enhanced the antiviral ability of cells against the virus, which indicated that OdTBK1 participated as a crucial factor in the host antiviral innate immune response.
Figure 8. Antiviral assay on OdTBK1. (A,B) EPC cells seeded in 24-well plates overnight were transfected with 0.5 μg OdTBK1-Myc or pCMV-Myc vector. At 24 h after transfection, the EPC cells were infected with SVCV (MOI = 0.01) per well and incubated at 28°C. The culture media was then harvested to detect the virus titers at 48 h post infection. (A) The cell monolayers were fixed with 4% PFA for 1 h and stained with 1% crystal violet overnight. (B) The viral titers of the supernatants were determined by TCID50 assays on EPC cells. The experiments were performed for three times with similar results.
As a key positive IFN regulator, TBK1 has been extensively studied in mammals, whereas studies of teleost TBK1 are rare. In this study, we describe a fish TBK1 isolated from O. obscura and its kinase function in inducing IFN expression and phosphorylating IRF3. These data demonstrate that TBK1 is conserved in both lower and higher vertebrates.
In our study, phylogentic analysis of the TBK1 amino acid sequences revealed that dark sleeper TBK1 is closely related to that of other fish and is likely an ortholog of mammalian TBK1s. This is consistent with TBK1 being the crucial kinase in IFN response, an essential and pivotal part of antiviral defense. In addition, other RLR factors such as MAVS, MITA, and IRF3 are conserved and functional in fish. Generally, IFN production activated by the RLR axis is necessary for both fish and mammal antiviral processes.
The tissue expression pattern indicated that OdTBK1 was highest in the pituitary, but relatively low in the spleen and head kidney. This is interesting because the pituitary participates in the formation of the hypothalamic–pituitary–interrenal axis for regulating the metabolism, immune response, and growth of fish generally (27, 28). The lower expression level of OdTBK1 in the head kidney and spleen is probably because OdTBK1 is not necessary in immune-relevant tissues of healthy fish. Also, OdTBK1 nay not be involved in adaptive immune processes.
In mammals, the induction of IFN and downstream ISGs symbolizes antiviral post infection response (29, 30). Similar to this, our study revealed that OdTBK1 exhibits a powerful effect on zebrafish and grass carp IFN promoter activation. Overexpression of OdTBK1 up-regulates the expression of fmifn and fmvig1, but not of fmmavs. MAVS belongs to the IFN-related gene and recruits TBK1/IKKε by TRAFs, which means that MAVS is not the TBK1 downstream effector protein (31). Furthermore, fish MAVS has been reported to contribute to IFN antiviral immunity upstream of TBK1 and IRF3/7 (32). These findings explain why TBK1 cannot directly up-regulate the expression of fmmavs.
OdTBK1 was located in the cytoplasm with or without poly I:C and SVCV, indicating that TBK1 activates downstream signal molecules from the cytoplasm and that the cytoplasm is where TBK1 is regulated by upstream molecules. After being stimulated by TBK1, dimerized and phosphorylated IRF3 transfers from the cytoplasm to the nucleus, where it binds to ISRE motifs to initiate the transcription of target genes, including IFN and other ISGs (33). As a critical kinase involved in antiviral immunity, TBK1 activity can be regulated in a variety of ways, such as phosphorylation, ubiquitination, and kinase activity modulation. These modifications occur mainly in the cytoplasm. For instance, E3 ubiquitin ligase TRAF3 mediates lysine 63 (K63)-linked polyubiquitination of TBK1 and facilitates its activation in the cytoplasm (34). These data support the cytoplasmic localization of TBK1 as responsible for its activation and function.
Research has indicated that OdTBK1 exhibited kinase activity that induced the phosphorylation of DrIRF3. We have characterized OdIRF3, but do not yet know whether OdIRF3 can be phosphorylated by OdTBK1. The protein kinase domain of OdTBK1 was indispensable for its kinase activity; the dominant negative mutant TBK1-K38M of human or crucian carp is able to effectively block this activity (20, 33). Future studies are needed to construct the mutant OdTBK1-K38M to determine conservation of the kinase functional site.
In summary, we have identified and characterized OdTBK1 and verified the partial function of TBK1 in host antiviral innate immunity. More research is still needed to understand the molecular mechanisms behind the biological functions and regulation of the TBK1-mediated signaling pathway and to gain insight into the potential role of OdTBK1 in fish.
SL conceived and designed the experiments. SL, JC, ZL, LL, PL, and X-YL performed the experiments and analyzed the data. SL, JC, and ZC wrote the manuscript. All authors reviewed the manuscript.
This work was supported by National Natural Science Foundation of China Grants 31502200 (SL).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: TBK1, IFN, RLRs, antiviral, Odontobutis obscura
Citation: Chen J, Li ZC, Lu LF, Li P, Li X-Y and Li S (2019) Functional Characterization of Dark Sleeper (Odontobutis obscura) TBK1 on IFN Regulation. Front. Immunol. 10:985. doi: 10.3389/fimmu.2019.00985
Received: 15 November 2018; Accepted: 16 April 2019;
Published: 03 May 2019.
Edited by:Stephanie DeWitte-Orr, Wilfrid Laurier University, Canada
Reviewed by:Sarah J. Poynter, University of Waterloo, Canada
Nguyen (Nathan) T. K. Vo, McMaster University, Canada
Copyright © 2019 Chen, Li, Lu, Li, Li and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Shun Li, firstname.lastname@example.org
†These authors have contributed equally to this work