Non-Structural Protein 3 of Duck Tembusu Virus Induces Autophagy via the ERK and PI3K–AKT–mTOR Signaling Pathways

Despite autophagy’s pivotal role in the replication of viruses such as duck Tembusu virus (DTMUV), which has caused massive economic losses to the poultry industry in the world, the specific relationships between DTMUV and cellular autophagy remain largely unknown. In response, we investigated the interactions between autophagy and DTMUV, the effects of the structural and non-structural proteins of DTMUV on autophagy, and the autophagy-related signaling pathways induced by DTMUV. Among the results, DTMUV increased the autophagy flux in duck embryo fibroblasts (DEF) and BHK-21 cells, while autophagy facilitated viral replication. After we pharmacologically induced autophagy with rapamycin (RAPA), the replication of DTMUV increased by 15.23-fold compared with the control group of DEF cells. To identify which DTMUV protein primarily induced autophagy, all three structural proteins and seven non-structural proteins of DTMUV were transfected into cells, and the results showed that non-structural protein 3 (NS3) induced significant autophagy in DEF cells. By means of Western blot, immunofluorescence, and transmission electron microscopy, we confirmed that NS3 protein could significantly induce autophagy and autophagy flux. Furthermore, we showed that NS3 induced autophagy in DEF cells through extracellular signal-regulated kinase 2 (ERK2) and phosphatidylinositol-3-kinase (PI3K)/AKT and the mammalian target of rapamycin (mTOR) signaling pathways using specific inhibitors and RNA interference assays. Finally, autophagy induced by NS3 promoted DTMUV replication. These results provide novel insight into the relationship between DTMUV and autophagy, broadening the current understanding of the molecular pathogenesis of DTMUV.


INTRODUCTION
In April 2010, duck Tembusu virus (DTMUV) was identified as the causative agent of egg drop syndrome, a condition among egg-laying and breeder ducks in China characterized by depression, a substantial decrease in egg laying and growth, and signs of neurological degradation (1). Since then, expanding host profiles of DTMUV infection have revealed that it can infect not only ducks but chickens and geese as well (2). Even BALB/c mice infected with DTMUV have shown serious systemic and neurological symptoms (3). Moreover, when positive DTMUV antibodies were detected in the sera of workers at duck farms (4), the virus became known not only for causing tremendous economic losses in the poultry industry but also as a potential zoonotic pathogen that could threaten public health (5).
DTMUV is a single-stranded RNA virus belonging to the Flavivirus genus of the Flaviviridae family; this genus also includes many mosquito-borne flaviviruses, such as dengue virus (DENV), West Nile virus (WNV), Zika virus (ZIKV), and Japanese encephalitis virus (JEV) (6). DTMUV possesses a genome approximately 11 kb long that encodes three structural proteins (C, prM, and E) and seven non-structural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5) (7). Whereas the structural proteins primarily mediate the virus' life cycle and fusion in the formation of viral particles (8,9), the non-structural ones engage in viral replication, virion assembly, and innate immune evasion (10). NS3 is a multifunctional protein with three different activities, which are determined by serine protease, RNA helicase, and triphosphatase, respectively (11). NS3 also plays a non-enzymatic role in autophagy, fatty acid biosynthesis, and actin polymerization, all of which are mediated by its recruitment of host proteins from various cellular pathways (12).
Autophagy represents an intracellular catabolic pathway highly conserved among eukaryotes that entails the removal of long-lived, aggregated, unfolded proteins and damaged organelles, as well as the regulation of growth and senescence (13). Autophagy is monitored by the lipidation rate of microtubule-associated protein 1 light chain 3 (LC3) and the degradation of polyubiquitin-binding protein sequestosome 1 (SQSTM1/p62, and p62 hereafter) (14). When autophagy occurs, LC3 will be converted from LC3-I to LC3-II with phosphatidylethanolamine by E3-like conjugation enzymes, which are located on autophagosomes (15). Autophagy is regulated by many factors, including pathogenic microbial infections (16), hunger, and other adverse environmental factors (17). In addition, a variety of signal pathways are also involved in the regulation of autophagy. At present, there are many studies on adenosine 5′-monophosphate (AMP)-activated protein kinase (AMPK), extracellular signal-regulated kinase 2 (ERK2), AKT-mTOR, and so on (18).
Given the surprisingly close relationship between numerous viruses and autophagy (19), some viruses have evolved mechanisms to inhibit autophagy in infected cells in order to survive in hosts. In WNV, for instance, the capsid protein can inhibit autophagy via the AMPK pathway (20). Other flaviviruses, however, including DENV and JEV, have evolved mechanisms to benefit from autophagy (20). Recent studies have shown that DTMUV infection can induce autophagy in vitro, particularly by promoting viral replication by decreasing the phosphorylation of TANK-binding kinase 1 (TBK1) and inhibiting antiviral immune responses (21). In vivo, autophagy can also facilitate DTMUV replication and thus aggravate the development of pathological symptoms (22). Despite such knowledge, the specific molecular mechanism of autophagy triggered by DTMUV remains unclear. Because those structural and non-structural proteins of DTMUV play important roles in autophagy and viral replication (23), we screened for the viral protein that induces autophagy and studied the autophagy-related pathways that it mediates. Our results suggested that the non-structural protein NS3 can induce autophagy and thus affect viral replication through the ERK2 and PI3K-AKT-mTOR signaling pathways.

Ethics Statement
This study was carried out in accordance with the Guide for the Care and Use of Laboratory Animals of the Shandong Agricultural University.

Cells, Virus, and Drugs
BHK-21 cells were obtained from the China Center for Type Culture Collection (Wuhan, China); the cell transfer algebra is within 10-20 generations. Duck embryo fibroblast (DEF) cells were isolated from 10-day-old duck embryos using trypsin digestion. Due to primary cell reasons, the transfer algebra is only within 1-3 generations. Both cells were cultured in Dulbecco's modified Eagle's medium (DMEM; Gibco, Langley, OK, USA) supplemented with 10% fetal bovine serum (Biological Industries, Beit HaEmek, Israel) at 37°C in 5% CO 2 in a humidified incubator. The DTMUV FX2010 strain (accession: MH414568.1) proliferated on the BHK-21 cells, and the cellular supernatant was collected for subsequent assays. The titer of the FX2020 strain was determined on DEF cells via a 50% tissue culture infectious dose (TCID 50 ) using the Reed-Muench method, in which the TCID 50 of the stock virus was 10 5.4 TCID 50 /100 µl. All drugs used in this study were purchased from MedChemExpress (MCE) company (Princeton, New Jersey,USA). When the cells were treated with 3-MA, cells were cultured in DMEM containing 3% FBS in a humidified incubator at 37°C with 5% CO 2 .

Transmission Electron Microscopy
DEF cells grown to 70%-80% confluence in 6-well plates were infected with PBS or DTMUV FX2010 or transfected with pCMV-HA and pCMV-HA-NS3, respectively, and treated by RAPA as the positive control. The DEF cells of different treatments in each group were collected and centrifuged for 5 min at 800-1,000 r/min, then the supernatant was discarded, cell sediment at the bottom of the centrifuge tube was collected, and the buffer was added. After being centrifuged for 5 min at 5,000 r/ min, the dense adherent cell pellet was collected. Then, we discard the supernatant and inject 2% to 4% glutaraldehyde (or a mixture of paraformaldehyde and glutaraldehyde), which was sent to Shandong Weiya Technology Co., Ltd., for transmission electron microscopy (TEM) observation. Images were obtained with a JSM-7500F transmission electron microscope (JEOL, Tokyo, Japan).

Transfection and RNA Interference
All 10 proteins of DTMUV were cloned into the pCMV-HA vector in order to construct recombinant plasmids, then were subsequently transfected into DEF and BHK-21 cells using Lipofectamine 3000 (Invitrogen, Carlsbad, CA, USA) in accordance with the manufacturer's instructions. Once the cells were collected at 24 h post-transfection (hpt) for Western blot analyses, DEF cells were grown in 6-well plates and transiently transfected with siRNAs ( Table 1) using a transfection reagent Lipofectamine RNAiMAX (Invitrogen, Carlsbad, CA, USA), also in accordance with the manufacturer's instructions. Knockdown efficiencies were determined by Western blot analysis. At 24 hpt, the cells were mock-infected with DMEM or inoculated with the FX2010 strain at a multiplicity of infection (MOI) of 0.3 and harvested at 36 h postinfection (hpi). The infected cells were harvested for the following assays.

mRFP-GFP-LC3 Transfection
BHK-21 cells were seeded onto glass coverslips in 24-well plates, and the mRFP-GFP-LC3 plasmid was subsequently transfected into cells using Lipofectamine 3000 (Invitrogen, Carlsbad, CA, USA) in accordance with the manufacturer's instructions. After being transfected for 24 h, BHK-21 cells were transfected with NS3, infected with virus, or treated with other drugs for 24 h. A laser scanning confocal microscope (Leica, Wetzlar, Germany) was used to observe autophagy flux. Yellow (overlay of mRFP and GFP) fluorescence spots indicated early autophagosomes; red (mRFP alone) fluorescence spots indicated late autolysosomes.

Indirect Immunofluorescence Assay
DEF cells were seeded on coverslips and co-transfected with pEGFP-LC3 and 10 recombinant plasmids as well as empty vectors, respectively. At 24 hpt, the cells were fixed with 4% formaldehyde and permeabilized with 0.1% (v/v) Triton X-100 in PBS. The transfected DEF cells were probed with rabbit-origin anti-HA monoclonal antibody (Abcam, Cambridge, UK), and the HA recombinant proteins were visualized using Cy3 goat anti-rabbit immunoglobulin (IgG; Jackson, West Grove, PA, USA). All probed cells were observed under a Leica SPE confocal microscope (Wetzlar, Germany).

Real-Time Quantitative PCR
Total RNAs were extracted from cells using the GeneJET RNA Purification Kit (Thermo Scientific, Waltham, MA, USA) and reverse-transcribed using the ReverTra Ace qPCR RT Kit (Toyobo, Osaka, Japan) according to the manufacturers' instructions. The specific primer of the DTMUV E gene and reaction conditions were reported previously (24), and the relative quantitative PCR (qPCR) was used to quantify the E gene expression with abundant b-actin mRNA as the internal control. All qPCR tests were performed using the SYBR Green Real-Time PCR Master Mix (Toyobo, Osaka, Japan) using a LightCycler 96 (Roche, Basel, Switzerland).

Western Blot Analysis
Cellular proteins were separated by 8%-12% SDS-PAGE and transferred to polyvinylidene difluoride membranes (Millipore, Bedford, MA, USA) using a semidry transfer apparatus (Bio-Rad, Hercules, CA, USA) in accordance with standard procedures. The primary antibodies used for detecting viral and host proteins included the monoclonal antibody against DTMUV E protein, the HA antibody (3724S; Cell Signaling Technology, Boston, MA, USA), an anti-b-actin IgG (4970T; Cell Signaling Technology), anti-cell autophagy signal pathway proteins, and their phosphorylated protein antibodies (Cell Signaling Technology)-that is, PI3K (4249T), AKT (4691T and p-AKT 4060S), mTOR (2983T and p-mTOR 5536T), and ERK2 (4695T and pERK2 4370T). Autophagy marker proteins LC3 (L8918) and P62 (P0067) were purchased from Sigma (San Francisco, CA, USA). Monoclonal antibody E was obtained from mice, and other antibodies were rabbits. Horseradish peroxidase-conjugated anti-mouse and anti-rabbit antibodies (Jackson, Lancaster, PA, USA) were used as secondary antibodies. Protein bands were visualized using the Clarity Western ECL substrate (Bio-Rad, Hercules, CA, USA).

Statistical Analysis
The data were recorded as the M ± SD of at least three independent experiments. SPSS version 25.0 (SPSS Inc., Chicago, IL, USA) was used for statistical analysis, and p value was calculated with a two-tailed paired or unpaired Student's t test in GraphPad version 8.0 (Prism, San Diego, CA, USA). Values of p < 0.05 were considered to be statistically significant, *p < 0.05; **p < 0.01.

The NS3 of DTMUV Induces Autophagy
To monitor autophagy after DTMUV infection, we analyzed the change of autophagic marker protein LC3. As shown in Figures 1A, B, the expression of LC3-II significantly increased at 24 and 48 hpi in BHK-21 and DEF cells infected with DTMUV, whereas the amount of LC3-II in the mock group did not increase as significantly. The results of Western blot also demonstrated that the accumulation of LC3-II increased with viral replication, especially in the late stages of DEF cell infection. Statistical analysis showed that autophagy levels of the mock group and virus infection group were significantly different (p < 0.01).
To further identify which proteins of DTMUV induced autophagy, we individually cloned all 10 genes (C-NS5) of DTMUV into the pCMV-HA vector and transfected into DEF cells to detect protein expression and autophagy by Western blot. The results indicated that all proteins could be expressed ( Figure 1C). Next, we detected the change in the LC3-II protein and found that the E, NS3, NS4A, and NS4B proteins could significantly increase its amount and decrease the expression of P62, thereby suggesting that they might induce autophagy in DEF cells ( Figure 1C). To provide additional evidence, pEGFP-LC3 and viral protein plasmids were cotransfected DEF cells for 24 h. Afterward, confocal microscopy was used to analyze the punctate accumulation of the fluorescent LC3 and its co-localization between LC3 and viral proteins in the transfected cells. As shown in Figure 1D, a strong, green punctate accumulation of the pEGFP-LC3 protein in the cytosol was observed in the cells expressing NS3 protein, and NS3, marked as red, was entirely located in the cytoplasm in an aggregated manner, whereas the control GFP protein diffusively distributed throughout the cell transfected with pCMV-HA. There was a high degree of co-localization between NS3 and pEGFP-LC3 proteins. According to those results, we speculated that NS3 could induce autophagy in DEF cells.
To study the characteristics of autophagy induced by NS3, we observed the LC3-II protein at 24 and 36 hpt. As shown in Figure 1E, compared with the empty vector group, the content of LC3-II in cells transfected with pCMV-HA-NS3 increased significantly from 24 to 36 hpt (p < 0.05); moreover, the autophagy level induced by NS3 is significantly higher than those of mock-trans and pCMV-HA ( Figure 1E). Further studies showed that NS3 protein could increase the transcription level of autophagy-related gene ATG5 (p < 0.05), and 3-MA could effectively inhibit NS3-induced autophagy in DEF cells 24 h after transfection ( Figure 1F). Because the formation of autophagosomes more directly determines whether NS3 triggers autophagy, we first observed the formation of autophagosome-like vesicles in DEF cells by the TEM method. In this study, we use Rapa treatment in DEF cells as a positive control and found some autophagosome-like vesicles ( Figure 1G) in Rapa-treated DEF cells; a similar phenomenon occurred in the virus-infected group, but just a few in mock cells. Interestingly, we also observed the fusion of autophagosomes and lysosomes in the group transfected with the

NS3 Can Cause Complete Autophagy Flux
To further investigate whether autophagy induced by NS3 was dose-dependent, we transfected pCMV-HA-NS3 and empty vector plasmids with 1, 2, and 3 mg, respectively; the results revealed a significant dose-dependent relationship between autophagy and NS3 protein (Figure 2A). Previous results showed a decline in the P62 protein ( Figures 1A, B), which suggested that DTMUV can cause complete autophagy flux in cells. Bafilomycin A1 disrupts autophagic flux by inhibiting both V-ATPase-dependent acidification and Ca-P60A/SERCAdependent autophagosome-lysosome fusion (25). Therefore, to further investigate whether NS3 can cause complete autophagy flux, DEF cells were treated with Bafilomycin A1 and then transfected NS3 protein. The results showed that after inhibition of autophagy flux, the continued expression and accumulation of LC3-II were caused by autophagy induced by the NS3 protein ( Figure 2B). Statistical analysis showed that LC3-II levels of the NS3-transfection group and NS3 and Bafilomycin A1 co-treatment group were significantly different (p < 0.01). Moreover, we want to study the phenomenon of NS3induced autophagy flux further and more intuitively, as shown in Figure 2C; after transfection with mRFP-GFP-LC3 in BHK-21 cells, we observed that the number of red fluorescence spots indicating late autolysosomes was significantly increased in the NS3 and FX2010 groups compared with the control group. However, the intensity of green fluorescence decreased, indicating that green fluorescence quenching was caused by an acidic environment when virus or NS3 induced autophagy. To sum up, NS3 can cause complete autophagy flux.

NS3 Induces Autophagy by Promoting the Phosphorylation of ERK2
Several studies have demonstrated that autophagy is associated with the ERK1/2 signaling pathway (26). ERK2 is a homologous analogue of ERK1/2 in duck, so we mainly detected the changes of ERK2 in DEF cells infected with DTMUV and transfected with the NS3 plasmid. We found that infection with virus or transfection with NS3 significantly increased the phosphorylation of ERK2 (Thr202 and Tyr204) (p < 0.01), accompanied by the accumulation of the LC3-II protein ( Figures 3A, B). U0126 could inhibit the phosphorylation level of ERK, which can treat the increase of LC3-II induced by virus ( Figure 3B) or NS3. These results suggest that ERK2 is involved in NS3-induced autophagy. Furthermore, we designed siRNAs for ERK2 and verified their effects, which revealed that the interference effect of siRNA317 was the most significant difference (p < 0.01) ( Figure 3C). DEF cells were pretreated with siRNA317 for 24 h and then infected with virus or transfected with NS3 protein. The levels of intracellular autophagy and ERK2 phosphorylation were measured. The results showed that inhibition of ERK2 phosphorylation could reduce the level of virus-induced autophagy ( Figure 3D). In the same way, DEF cells were treated with siRNA317 prior to NS3 transfection. The results revealed that NS3-induced autophagy was repressed in the pretreated cells with siRNA317 ( Figure 3E).
To sum up, NS3 induced autophagy by promoting the phosphorylation of ERK2.

NS3 Induces Autophagy by Inhibiting the Phosphorylation of PI3K-AKT-mTOR
In our study, we found that NS3 protein inhibited the phosphorylation of AKT and mTOR compared with the empty vector, and the expression of PI3K decreased in the NS3 transfection group ( Figure 4A). To further determine the role of this signaling pathway in NS3-induced autophagy, IGF-1, a physiology activator of AKT/mTOR, was selected for treatment, and the function of IGF-1 in DEF cells had been verified, as shown in Figure 4B; it was found that IGF-1 could significantly reduce the increase of autophagy induced by NS3 protein and DTMUV ( Figure 4A). To further determine the role of PI3K in NS3-induced autophagy, we treated DEF cells with LY294002, which can regulate autophagy via PI3K, before transfecting NS3. As shown in Figure 4C, the effect of LY294002 on PI3K expression was also verified in DEF cells. Treatment with LY294002 resulted in decreased ratios of LC3-II in NS3transfected cells compared with the group transfected with NS3 recombinant plasmid alone, thereby demonstrating that LY294002 effectively inhibits autophagy induced by NS3 ( Figure 4D). These results suggest that PI3K is involved in NS3-induced autophagy. To sum up, these results further demonstrated that DTMUV NS3 protein induced autophagy via the PI3K-AKT-mTOR pathway in DEF cells.  as high as that in the mock group and the 3-MA-treated group. At 36 hpi, the expression of the E gene in the RAPA-treated group was 3.2-fold and 10.3-fold higher than that in the mock and 3-MA groups, respectively. As for infection with DTMUV after 48 h, the virus replicated rapidly, and the difference between the RAPA-treated group and the other two groups widened (p < 0.01). In addition, protein samples at 36 h were also collected to detect the expression of E protein; the results showed that the E protein in the RAPA-treated group was significantly higher than that in the other two groups. Consistently, 3-MA inhibited the replication of DTMUV ( Figure 5B) (p < 0.01).
To determine whether autophagy induced by DTMUV NS3 also promotes viral replication, the groups were set up, as shown in Figure 5C, and the Western blot results showed that the overexpression of NS3 significantly promoted virus replication at 36 and 48 hpi compared with the empty vector group (p < 0.05). However, when autophagy induced by NS3 was inhibited by 3-MA or siRNA317, the ability of NS3 to promote replication was strongly inhibited (Figures 5D, E). At the same time, we measured the viral titer, and the results showed that inhibition of NS3-induced autophagy could reduce (p < 0.05) the viral titer of DTMUV ( Figure 5F). Those data suggest that autophagy induced by NS3 promotes the replication of DTMUV.

DISCUSSION
Autophagy is a catabolic pathway used by eukaryotic cells to counteract stress response, promote organelle turnover, and clear aggregated proteins and excess lipids (27), as well as degrade infectious microorganisms and participate in the regulation of immune responses (28). In those ways, autophagy protects cells from damage and maintains cellular homeostasis (29). A complex relationship exists among autophagy, viruses, and their hosts. In this study, we first verified the interaction between DTMUV and autophagy; the results are consistent with the previous report (21). DTMUV infection can induce autophagy, and autophagy can promote virus replication. More importantly, we further studied the molecular mechanism of autophagy induced by DTMUV. Flavivirus encodes 10 proteins, of which 7 nonstructural proteins play important roles in the interactions between virus and host. Studies have shown that the NS4A of a variety of flaviviruses plays a vital role in inducing autophagy, such as DENV (30), WNV (31), and ZIKV (32). When expressed alone, NS4A can significantly induce autophagy and affect the replication and pathogenicity of these viruses. However, the C, M, and NS3 proteins of JEV are also reported as the main proteins that induce autophagy in BHK-21 cells (33). The NS4B protein of hepatitis C virus (HCV) was sufficient to induce the autophagic vacuoles (34). Moreover, the NS3/4A complex and the NS5 of HCV individually were also able to induce autophagy (35). In the current study, further expression of individual DTMUV proteins indicated that E, NS3, NS4A, and NS4B proteins could significantly increase the expression of LC3-II, and we further confirmed that DTMUV NS3 protein played a key role in inducing autophagy of DEF cells by immunofluorescence, Western blot, and TEM experiments, and NS3 had the ability to induce complete autophagic flux in DEF cells. NS3 ranks among the best-characterized non-structural proteins of flaviviruses, which is a multifunctional protein with serine protease, RNA helicase, and triphosphatase activities (36,37). Because the NS2B protein offlavivirus forms a stable complex with NS3 and acts as a cofactor for the NS2B-NS3 serine protease (38), we speculated that autophagy induced by NS3 has nothing to do with hydrolase, although the details warrant further examination. Interestingly, both the NS4A and NS4B proteins of DTMUV can also increase the amount of LC3-II. Considering the key roles of NS4A, 4B in other flavivirus-induced autophagy, especially NS4A, it is necessary to further verify the effect of DTMUV NS4A on autophagy.
Autophagy is a complex physiological metabolic process, which is affected by many factors, for example, PI3K-AKT-mTOR and the mitogen-activated protein (MAP) kinase ERK1/2 (39). In order to further clarify the signal pathway of autophagy induced by NS3 of DTMUV, inhibitors LY294002 and IGF-1-targeted PI3K-AKT-mTOR signal were used, then they decreased the autophagy induced by NS3, indicating that DTMUV NS3 protein could induce the autophagy of DEF cells through the PI3K-AKT-mTOR signaling pathway. PI3K-AKT-mTOR is a classic pathway for flaviviruses to regulate autophagy, and it has been reported that DENV NS4A can activate autophagy in a PI3Kdependent manner (30). Interestingly, ZIKV NS4A and NS4B have been shown to induce the autophagy of human fetal neural stem cells by deregulating the AKT-mTOR signal pathway (40), and HCV could also induce endoplasmic reticulum stress (ERS)mediated unfolded protein response and inhibit the AKT-mTOR pathway to trigger autophagy (41). Besides, it has been reported that HCV NS3 might interact with ATG5 and ATG10 via immunityrelated GTPase family M protein (IRGM) to induce autophagy, and IRGM is critical for HCV-induced autophagy, as its depletion suppressed HCV-induced autophagy (42). In fact, we also identified the host proteins that may interact with DTMUV NS3 by mass spectrometry and did not find IRGM and autophagyrelated proteins but identified a variety of other proteins, such as heat shock protein (HSP) 90a, HSP90b, and HSP70. The specific interactions between them and NS3 and their roles in NS3-induced autophagy will be focused in our further study.
Recent studies have shown that infectious bronchitis virus can induce autophagy by ERK1/2 and play a pro-survival role at the late stage of IBV infection (43). Autophagy can be induced through ERK1/2 in PCV2-infected cells (44). JEV infects mouse microglia resulting in the activation of ERK/MAPKp38/ AP-1/NF-kB signaling cascades, leading to the production of inflammatory cytokines (45), but it is not known whether ERK1/ 2 is related to autophagy induced by JEV. In this study, we found that DTMUV and NS3 protein can induce the phosphorylation of ERK2 in DEF cells, and the use of U0126 and interference RNA-targeted ERK2 can significantly inhibit DTMUV-and NS3-induced autophagy, indicating that ERK2 was required for the NS3-induced autophagy. Moreover, ERK2 regulated inactivated Sendai virus and induced autophagy in HeLa cells by inhibiting the PI3K-AKT-mTOR pathway (46). However, the relationships between the PI3K-AKT-mTOR and ERK2 signaling pathways in our study require further study.
The relationship between virus replication and autophagy is complicated, and the propagation of some viruses is suppressed by autophagy, whereas other viruses can hijack autophagy to promote their replication (47), such as autophagy which positively regulates JEV replication by regulating the early step of virus replication in neuronal cells (48), and autophagy activation has been found to increase the titer of DENV and enhance its pathogenicity in mice (49,50), but it has also been reported that autophagy induced by WNV inhibits virus replication (36). Our results are consistent with previous reports that DTMUV-induced autophagy can enhance self-replication in vivo and in vitro (22), and NS3induced autophagy can indeed promote virus replication. The possible mechanism was that DTMUV inhibited TBK-1 phosphorylation through P62 degradation in DEF cells, which led to the decrease of NF-kB and IRF3 phosphorylation and ultimately inhibited the expression of IFN-I and IL-6 (21).
In sum, the NS3 protein of DTMUV can induce autophagy in DEF cells via the ERK2 and PI3K-AKT-mTOR signaling pathways, while autophagy induced by NS3 can promote viral replication. Those results illuminate the pathogenesis of infection with DTMUV and provide novel insights into the development of effective therapeutic strategies.

DATA AVAILABILITY STATEMENT
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding authors.

AUTHOR CONTRIBUTIONS
JZ performed the most experiments, analyzed data and wrote the manuscript. TZ and GC made great efforts to revise the manuscript, NG, ZG, SC and YY helped construct the pCMV-HA-FX2010 plasmids. KL, SW, YZ and FM performed some western blot experiments. SL and MJ designed some experiments, NL designed the whole study and reviewed the article. All authors contributed to the article and approved the submitted version.