key: cord-0881510-4u81tog4
authors: Zhang, Huihui; Song, Xingdong; Li, Tianxu; Wang, Jinchao; Xing, Bin; Zhai, Xinyu; Luo, Jinjian; Hu, Xiaofang; Hou, Xiaolan; Wei, Liangmeng
title: DDX1 from Cherry valley duck mediates signaling pathways and anti-NDRV activity
date: 2021-01-20
journal: Vet Res
DOI: 10.1186/s13567-020-00889-4
sha: acb2c046b28978a066077053d25e87abd6355c1e
doc_id: 881510
cord_uid: 4u81tog4

Novel duck reovirus (NDRV) causes severe economic losses to the duck industry, which is characterized by hemorrhagic spots and necrotic foci of the livers and spleens. DEAD-box helicase 1 (DDX1) plays a critical role in the innate immune system against viral infection. However, the role of duck DDX1 (duDDX1) in anti-RNA virus infection, especially in the anti-NDRV infection, has yet to be elucidated. In the present study, the full-length cDNA of duDDX1 (2223 bp encode 740 amino acids) was firstly cloned from the spleen of healthy Cherry valley ducks, and the phylogenetic tree indicated that the duDDX1 has the closest relationship with Anas platyrhynchos in the bird branch. The duDDX1 mRNA was widely distributed in all tested tissues, especially in the duodenum, liver, and spleen. Overexpression of duDDX1 in primary duck embryo fibroblast (DEF) cells triggered the activation of transcription factors IRF-7 and NF-κB, as well as IFN-β expression, and the expression of the Toll-like receptors (TLR2, TLR3, and TLR4) was significantly increased. Importantly, after overexpressing or knocking down duDDX1 and infecting NDRV in DEF cells, duDDX1 inhibits the replication of NDRV virus and also regulates the expression of pattern recognition receptors and cytokines. This indicates that duDDX1 may play an important role in the innate immune response of ducks to NDRV. Collectively, we first cloned DDX1 from ducks and analyzed its biological functions. Secondly, we proved that duck DDX1 participates in anti-NDRV infection, and innovated new ideas for the prevention and control of duck virus infection.

The new duck reovirus (NDRV) is a double-stranded RNA (dsRNA) virus and a member of the Orthoreovirus genus in the Reoviridae family. The genome of the virus consists of 10 genome segments, L1-3, M1-3 and S1-4 [1] . The encoded NDRV S1 segment is similar to avian reovirus (ARV) [2] , with three partially overlapping open reading frames (ORFs), encoding p10, p18, and σC, respectively [3] . Among them, σC can produce specific neutralizing antibodies, and p17 protein can inhibit the host immune response and affect the regulatory response of interferon.

In the process of virus replication, first, the virusencoded dsRNA-dependent RNA polymerase uses the negative-strand RNA of the viral genome as a template to synthesize mRNA. Subsequently, the viral mRNA completes the capping reaction when it leaves the viral core through the channel formed by the capping enzyme λC [4] . Finally, viral mRNA plays a dual function in the infected cell, synthesizing viral proteins in the ribosome and as a template to synthesize viral genome negativestrand RNA.

NDRV infection mainly causes hemorrhage and necrosis of the liver and spleen, and may also lead to the transfer of intestinal flora1 [5] , which is different from diseases Open Access [6] . Since it was first discovered in China in 2005, it has caused serious economic losses in the duck industry. Although there are many reports about the identification and diagnosis of NDRV [6] [7] [8] , there are few reports about NDRV inducing host antiviral natural immune response.

Pattern recognition receptors (PRRs) are located on multiple types of innate immune cells, and can initiate immune responses to specific pathogen-associated molecular patterns (PAMPs) exclusively present on microbes (such as viruses, bacteria, parasites, and fungi) [9, 10] . PRRs include the Toll-like receptors (TLRs), the retinoic acid-inducble gene I-like receptors (RLRs), the nucleotide oligomerization domain-like receptors (NLRs) and cytosolic DNA sensors [11, 12] . Once PAMPs were recognized, the signal triggered by PRRs will activate downstream signaling pathways to induce type I interferon (IFN-I) and other pro-inflammatory cytokines, thereby establishing an antiviral immune system [13, 14] . IFN-I mainly inhibits the replication and spread of the virus by producing Interferon-stimulated genes (ISGs) [15] .

DEAD-box helicases belong to the helicase superfamily 2 (SF2) and share at least eight conserved sequence motifs (motifs I, Ia, Ib, II, III, IV, V, and VI) spread, and are named DEAD-box helicases because they contain Asp-Glu-Ala-Asp (DEAD) [16] . The DEAD-box helicases core consist of two RecA-related domains. In addition to the helicase core, DEAD-box helicases usually also contains N and C-terminal extensions that provide specificity for RNA and/or protein interactions [17] . DEAD-box helicases play crucial roles in RNA metabolism such as splicing, ribosome biogenesis, RNA transport, degradation and translation [18] .

DEAD-box helicase 1(DDX1), a member of the DEADbox RNA helicases family, and was first discovered in retinoblastoma and neuroblastoma in 1993 [19] . Previous experiments proved that DDX1 can play a role in cell proliferation and RNA metabolism of differentiated cells, especially to elevate the level of DDX1 in neuroectoder [20] . DDX1 can bind to the subunit of NF-κB RelA, and enhance NF-κB-mediated gene expression [21] . In addition, DDX1 can participate in the transfer of RNA between the cytoplasm and the nucleus and the cleavage of tRNA [22, 23] , and DDX1 is a cofactor of the miRNA cleavage processing enzyme Drosha, which can regulate the post-transcriptional maturation of miRNA [23] . DDX1 can also regulate insulin translation after binding to insulin Mrna [24] . It suggesting that DDX1 is involved in multiple cellular processes of RNA metabolism.

Although DDX1 has been studied in human [25] , chicken [20] and mice [26] , it has not been found in ducks. In this study, we cloned the duck-derived DDX1 from Cherry valley duck spleen, analyzed its biological characteristics and its expression in various tissues, and studied the role of duDDX1 in RNA viruses, especially in NDRV infections. It is expected to provide a reference for the in-depth study of duDDX1 in the way to regulate the host's innate immune mechanism.

Cherry valley ducks were purchased from a farm in Tai'an, China. Primary duck embryo fibroblast (DEF) cells were extracted from 10-day-old duck embryos and cultured in DMEM (GIBCO, Grand Island, NY, USA) with 10% fetal bovine serum (GIBCO, Grand Island, NY, USA). DEF cells were incubated at 37 ℃ in a 5% CO 2 incubator. New duck reovirus (NDRV) was previously preserved in the laboratory [27] .

To clone the duck DDX1 (duDDX1), primers DDX1-F and DDX1-R (Table 1) were designed based on the predicted duck sequence from the National Center for Biotechnology Information (NCBI). Total RNA was extracted from duck spleen via TransZol up (Vazyme, Nan jing, China) and reverse transcription into cDNA using a HiScript ® II Q RT SuperMix for qPCR (Vazyme, Nan jing, China).

Amino acid sequences deduced from the nucleotide sequences were aligned using Clustal X and edited with DNAMAN. The structure domain of duDDX1 is identified via SMART program. Sequence homology analysis was conducted using MegAlign (DNAstar, USA). The phylogenetic tree was constructed based on DDX1 from 15 different species, including birds, fishes, and mammals.

Three health ducks (aged 3 weeks) were killed and their tissues including the heart, liver, spleen, lung, kidney, brain, cerebellum, muscle, cecum, ileum, jejunum, duodenum, windpipe, bursal of fabricius, muscular stomach, glandular, stomach, skin, esophagus, pancreas, and brainstem were collected [28] . Twenty-eight health ducks (aged 3 weeks) were randomly divided into two groups, one group was used for an infection experiment in which ducks were intramuscularly inoculated with 0.5 mL virus stocks containing 1.0 × 10 4.5 TCID 50 . The other group was set as the control group and received an intramuscular injection of 0.5 mL sterile PBS [29] . On 1, 3, and 5 days post-infection (dpi), three ducks from each group were killed and their liver and spleen were collected.

Total RNA was extracted for duDDX1 mRNA expression detection from these tissues.

The expression construct pcDNA3.0-duDDX1-Flag was constructed by inserting full-length duDDX1 into the BamH-I and Not-I sites of the pcDNA3.0-Flag vector using Hieff Clone ™ Multi One Step Cloning Kit (Yeasen, Shanghai, China). The primers described in Table 1 .

Quantitative real-time PCR (qRT-PCR) was conducted via indicated primers (Table 1) using the LightCycler ® 96 SW 1.1 real-time PCR system. The qRT-PCR was performed using ChamQ ™ SYBR qPCR Master Mix (Vazyme, Nanjing, China), and performed at a reaction volume of 20 μl according to the manufacturer's instructions. The PCR cycling conditions were: 1 cycle at 95 °C for 300 s, 40 cycles of denaturation at 95 °C for 10 s, 60 °C for 34 s, and 97 °C for 1 s. The relative expression levels of the tested mRNAs were determined using GAPDH as an internal reference using the comparative Ct (2 −ΔΔCT ) method.

DEF cells were cultured in a 6-well plate. When the cells reached approximately 95% confluence, the pcDNA3.0-duDDX1-Flag or empty vector were transfected into the DEF cells, according to the instructions of Nulen Trans ™ Liposomal Transfection Reagent (NULEN BIOTECH, Shanghai, China). At 48 h post-transfection (hpt), cells were lysed with a cell lysis buffer containing Protease inhibitor cocktail (Beyotime, Shanghai, China), and cell proteins were collected. After SDS-PAGE electrophoresis and wet transfer, the target protein was transferred to polyvinylidene fluoride (PVDF) membrane (Solarbio, Beijing, China). Seal with 5% skimmed milk powder for 1 h, and then they were incubated with mouse anti-Flag antibody (Cell Signaling Technology, Shanghai, China) and Goat Anti-Mouse IgG, HRP Conjugated (CWBIO, Beijing, China). After membrane washing, the protein bands were observed with ECL kit (BIO-Rad), and images were collected using the Tanon 5200 imaging system (Tanon, Shanghai, China).

DEF cells were seeded in 24-well plates and cultured until the cells reached approximately 95% confluence, and then co-transfected with the pcDNA3.0-duDDX1-Flag or empty vector (500 ng/well), reporter plasmid (100 ng/ well), and pRL-TK plasmid (50 ng/well) by Nulen Trans ™ Liposomal Transfection Reagent (NULEN BIOTECH, Shanghai, China). Cell extracts were collected at the indicated time points and luciferase activity was measured with a dual-specific luciferase assay kit (Promega). All reporter assays were independently repeated at least three times. Table 1 Primer information table of this 

Three interfering RNA-targeting duDDX1 sequences were purchased from GenePharma (Shanghai, China). According to the instructions of Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA), three interfering RNAs and negative control (NC) were transfected into DEF cells in a 6-well plate. Their interference efficiency were analyzed by qRT-PCR after 36 hpt. The siRNA sequences were listed in Table 2 .

DEF cells were transfected with pcDNA3.0-duDDX1-Flag or empty vector, after 24 hpt, the transfected cells were washed twice and infected with 10 TCID 50 NDRV for 1 h. Or DEF cells were transfected with Si-DDX1 or Si-NC, after 36 hpt, the transfected cells were washed twice and infected with 1 TCID 50 NDRV for 1 h. The virus solution was discarded after the designated time, and add 2 mL of low serum medium (DMEM containing 2% fetal bovine serum) into each well to maintain the cells [27] .

All data were expressed as mean ± SE of three independent experiments. Significance was determined with the student t tests using SPSS software version 17.0 (SPSS Inc., Chicago, IL, USA). P < 0.05 were considered indicative of statistical significance.

The full-length cDNA of duDDX1 contains 2223 bp (GenBank accession number, MT978184) encoded 740 amino acid residues ( Figure 1A ). Using SMART software to analyze the protein domains of duDDX1, it was found that duDDX1 consists of a DEXDc domain (AA 21-444), a HELICc domain (AA 520-610), and a SPRY domain (AA 130-246) ( Figure 1B) . Multiple sequence comparisons indicated that duDDX1 showed relatively high identity with the DDX1 of chicken (98.6%), with 93.2% and 93% identity to pig and human DDX1 proteins, respectively (Figure 2A) . Phylogenetic analysis showed that duDDX1 was branched with birds and showed higher evolutionary relationship than with mammals and fishes ( Figure 2B ).

DuDDX1 mRNA expression is relatively higher in the duodenum, liver, and spleen, while lower in the kidney and esophagus ( Figure 3A ). The results of animal inoculation experiments showed that after NDRV infection, the expression of duDDX1 in the liver was significantly increased 4.3-fold (P < 0.001), while in the spleen decreased 2.8-fold (P < 0.01) ( Figure 3B ).

The western blot results showed that the band of protein expressed in DEF cells transfected with pcDNA3.0-duDDX1-Flag was about 82 KD (Figure 4) , which was consistent with the size of the target protein.

To determine the role of duDDX1 in duck innate immunity response, the pcDNA3.0-duDDX1-Flag or empty vector were transfected into DEF cells, and DEF cells were collected at designated time points for subsequent experiments ( Figure 5 ). Figure 5 shows that the mRNA expression levels of Toll-like receptors (TLR2, TLR3, and TLR4) were up-regulated after 12 hpt versus the control group. The mRNA expression level of TLR3 was up-regulated by 4.1-fold (P < 0.001) at 36 hpt. In addition, the mRNA expression levels of IFN-β and IFN-γ were upregulated both at 12 and 24 hpt versus the control group. The mRNA expression level of IFN-γ was up-regulated by 8.3-fold (P < 0.01) at 36 hpt.

To further demonstrate that duDDX1 is involved in the signaling pathway of IFN-β in DEF cells, we conducted the dual luciferase experiment ( Figure 6 ). The results showed that duDDX1 significantly activated the activity of IFN-β (3.2-fold, P < 0.01), and both IRF-7 and NF-κB promoters were involved in regulating duDDX1-induced IFN-β activation (4.5-fold, P < 0.001).

To analyze the effect of DDX1 on the proliferation of NDRV, DEF cells transfected with pcDNA3.0-duDDX1-Flag or empty vector were infected with NDRV. The changes of viral RNA were measured by qRT-PCR Table 2 The sequences of pSi-RNA. Figure 7A shows that compared with the control group, the copy number of NDRV at 36 h post-infection (hpi) was reduced by 3.0-fold (P < 0.001).

To verify this result, three interfering RNAs of duDDX1 were designed ( Figure 7B ). Figure 7B shows that Si-duDDX1-1 displayed the highest interference efficiency. Therefore, Si-duDDX1-1 was selected as the interfering RNA verify the above experimental results. The results showed that the inhibition of duDDX1 by siRNA interference showed increased NDRV replication ( Figure 7C ).

After overexpression or interference with duDDX1, DEF cells were stimulated by NDRV to investigate the changes in antiviral and innate immune response after NDRV infection.

We found that the Toll-like receptors (TLR2 and TLR4) involved in the antiviral response were up-regulated after viral stimulation (2.1-fold, P < 0.01), while TLR3 was down-regulated 1.7-fold (P < 0.05). The expression levels The neighbor-joining tree was generated using MEGA 7.0 [37] , and a 1000-replicate bootstrap analysis was performed. Scale bar is 0.02. GenBank accession numbers are shown in Table 3 .

of OAS and Mx mRNA were down-regulated by 7.0-fold (P < 0.001) and 5.4-fold (P < 0.001) at 24 hpi, respectively ( Figure 8) . Figure 9 shows that after virus stimulation, IFN-α, IFN-β, and IFN-γ were all up-regulated, and IFN-γ was up-regulated by 3.8-fold (P < 0.001) at 24 hpi. In addition, at 24 and 36 hpi, TLR2 and TLR4 were down-regulated, while TLR3 was up-regulated. At 48 hpi, PKR was up-regulated by 4.5-fold (P < 0.01). Gene knockdown is roughly the opposite of gene overexpression (Figure 9 ).

In this research, the complete DDX1 cDNA was cloned from Cherry valley duck for the first time. DuDDX1 encoded an amino-acid sequence of 740 residues. Based on the predicted amino acid sequence, bioinformatics analysis was performed. Like DDX1 of other species, duDDX1 contains three main domains: DEXDc domain (AA 21-444), HELICc domain (AA 520-610), and SPRY domain (AA 130-246). Multiple sequence alignment revealed that the amino sequence of duDDX1 was highly conserved among various species including mammals, birds and fishes. To investigate the tissue-specific distribution of duDDX1, the abundance of duDDX1 gene in different tissues was analyzed. DuDDX1 mRNA was detected in all test tissues. DuDDX1 is highly expressed in the duodenum, liver, and spleen. However, porcine DDX1 is abundantly expressed in fat, spleen and liver.

These results indicate that the distribution of DDX1 in different species is different. Western blot results show that the pcDNA3.0-duDDX1-Flag eukaryotic expression plasmid was successfully constructed and can be expressed in DEF cells.

To further explore the relationship between duDDX1 and host innate immunity, we found that overexpression duDDX1 in DEF cells up-regulated TLRs (TLR2, TLR3, and TLR4) and IFN-I (IFN-α, IFN-β, and IFN-γ) , however, some cytokines (IL-6, IL-8, IL-1β, and TNF) and RIG-I-like receptors (RIG-I and MDA5) did not change significantly.

In the host's innate immunity, type I IFN is a key cytokine, which can induce a large number of interferonstimulating genes against viruses [30] . Previous studies have confirmed that DDX1 can promote the production of type I IFN. According to reports, the RNA helicase complex composed of DDX1, DDX21 and DHX36 induces type I IFN through TRIF-dependent signaling in myeloid dendritic cells, and they can recognize short poly I: C (0.2-1 kb) and long poly I: C (1.5-8 kb) and reovirus [31, 32] . The non-structural protein 14 (nsp 14) encoded by Transmissible gastroenteritis virus (TGEV) interacts with DDX1 to induce the production of IFN-β [33] . We found that overexpression of duDDX1 can significantly activate the activity of IFN-β, and both IRF-7 and NF-κB promoters are involved in regulating duDDX1-induced IFN-β activation. This suggests that duDDX1 may be involved in inducing the expression of IFN-β.

In general, viral infection triggers the host's innate immune response through activation of PRRs [34] . DDX1 can interact with the nsp 14 protein from severe acute respiratory syndrome coronavirus (SARS-CoV) to enhance Avian infectious bronchitis virus (IBV) replication [35] . In addition, DDX1 can promote the proliferation of hepatitis C virus (HCV) [19] . DDX1 can also interact with the viral protein 3D and inhibit the replication of the foot-and-mouth disease virus [36] . Although DDX1 can inhibit or promote virus replication, however, the role of DDX1 during NDRV infection remains unclear. Our results showed that the replication of NDRV was significantly inhibited in DEF cells overexpressing duDDX1, while it was enhanced in DEF cells knocking down duDDX1, it can be concluded that duDDX1 can inhibit the proliferation of NDRV in vitro. These changes have a certain relationship with the natural immunity caused by the host infection with NDRV virus.

In this study, we cloned the full length CDs of duDDX1, to further study the role of duDDX1 in the host's innate immune response, Cherry valley ducks were infected with NDRV. The expression level of duDDX1 mRNA was up-regulated in the liver, but down-regulated in the spleen. This indicates that DDX1 may be involved in the anti-NDRV immune response, then we further verified it through in vitro cell experiments. By comparing the effects of overexpression or knockdown of duDDX1 on the immune response in DEF cells infected with NDRV, we found that after infection with NDRV virus, the expression of inflammatory cytokines decreased and the expression of TLRs changed significantly, except RIG-I receptors, we speculate that duDDX1 may regulate the expression of TLRs, thereby regulating the expression of interferons and viral stimulating factors. According to reports, NDRV can be recognized by several PRRs that initiate innate immunity [29] , which is similar to our results. As we concluded that duDDX1 can inhibit the replication of NDRV virus. In summary, NDRV has caused a huge economic losses to the breeding industry [8] , therefore, investigating the immune mechanism of duDDX1 defense against NDRV infection will provide a theoretical basis for further understanding of the antiviral innate immune response of ducks and the pathogenesis of inflammatory diseases. The experimental group was DEF cells transfected with pcDNA3.0-duDDX1-Flag, and the control group was DEF cells transfected with empty vector. Cells were collected at 24, 36, and 48 hpt, and the mRNA expression levels of pattern recognition receptors (TLR2, TLR3, and TLR4), pro-inflammatory cytokines (IL-6, IL-8, IL-1β, and TNF), interferons (IFN-α, IFN-β, and IFN-γ) and ISGs (PKR, OAS, and Mx) were analyzed by qRT-PCR. The relative expression of gene mRNA were calculated using the 2 −ΔΔCT method with GAPDH serving as a normalization gene and mean control values as baseline reference. Data are represented as the mean value ± SE of three experiments. A student t test was performed to assess the difference. * P < 0.05; ** P < 0.01; *** P < 0.001.

Overexpression of duDDX1 stimulates IFN-β expression. A dual luciferase reporter gene assay was used to study the IFN-β signaling pathway. PcDNA3.0-duDDX1-Flag or empty vector (500 ng/well) were co-transfected with reporter plasmids (100 ng/well) (A) pGL3-IFN-β; (B) pGL3-IRF-7; (C) pGL-NF-κB with pRL-TK (normalization) (50 ng/well). After 24, 36, and 48 hpt, cells were harvested, and luciferase activity was measured. Relative IFN-β-, IRF-7-, or NF-κB-reporter activation was calculated as fold-change in normalized Firefly luciferase activity with reference to mean control values set to 1. Data were means from three independent experiments and each experiment was analyzed in tri plicate. A student t test was performed to assess the difference. * P < 0.05; ** P < 0.01; *** P < 0.001.

DuDDX1 inhibits NDRV virus activity. A Transfected pcDNA3.0-duDDX1-Flag or empty vector in DEF cells for 24 h and then the cells were infected with 10 TCID 50 /mL NDRV. B SiRNA interference efficiency. DEF cells were transfected with Si-duDDX1-1 as the experimental group or transfected with Si-NC as the control group. The cells were collected at 36 hpt. QRT-PCR was used to detect the expression level of duDDX1 mRNA. C Transfected Si-duDDX1 or Si-NC in DEF cells for 36 h and then the cells were infected with 1 TCID 50 /mL NDRV. The culture supernatant (A, B are the same) were collected, and detected the virus titer at 24, 36, and 48 hpi by qRT-PCR. A student t test was performed to assess the difference. * P < 0.05; ** P < 0.01; *** P < 0.001.

anti-viral molecules after NDRV infection. DEF cells were transfected with pcDNA3.0-duDDX1-Flag as the experimental group, and DEF cells were transfected with empty vector as the control group. The cells were stimulated with 10 TCID 50 /mL NDRV after 24 hpt. At 24, 36, and 48 hpi, cells were collected and analyzed for inducible gene expression. The relative expression of gene mRNA were calculated using the 2 −ΔΔCT method with GAPDH serving as a normalization gene and mean control values as baseline reference. Data are represented as the mean value ± SE of three experiments. A student t test was performed to assess the difference. * P < 0.05; ** P < 0.01; *** P < 0.001.

Knocking-down duDDX1 expression reduces induction of some major innate immune and anti-viral gene expression after NDRV infection. DEF cells were transfected with Si-duDDX1-1 as the experimental group, and DEF cells were transfected with Si-NC as the control group. The cells were stimulated with 1 TCID 50 /mL NDRV after 36 hpt. Cells were collected and analyzed for inducible gene expression at 24, 36, and 48 hpi. The relative expression of gene mRNA were calculated using the 2 −ΔΔCT method with GAPDH serving as a normalization gene and mean control values as baseline reference. Data are represented as the mean value ± SE of three experiments. A student t test was performed to assess the difference. * P < 0.05; ** P < 0.01; *** P < 0.001.

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The authors would thank Tianxu Li 

Authors' contributions HZ wrote the manuscript and performed most of the experiments. TL revised the manuscript. XH, JW and XZ collected the samples and extracted the sample RNA. XS and BX kept animals. JL and XH analyzed the data. LW designed the study and reviewed the manuscript. All authors read and approved the final manuscript.

This work was supported by the National Natural Science Foundation of China (31972664), the China Postdoctoral Science Foundation (2018M632268 and 2019T120404) and the Shandong "Double Tops" Program (515_564013 and SYL2017YSTD11).

We have uploaded the acquired sequence of duDDX1 to GenBank (accession number, MT978184), and other datasets analyzed during the current study are available from the corresponding author on reasonable request.

All animal experiments were performed in accordance with the recommendations of the Shandong Agricultural University Animal Care and Use Committee. The approval number for this study is SDAUA-2019-011.

Written informed consent for publication was obtained from all participants.

The authors declare that they have no competing interests.