key: cord-0023107-zbysyonv
authors: Zhou, Minmin; Wang, Shaobo; Guo, Jiao; Liu, Yang; Cao, Junyuan; Lan, Xiaohao; Jia, Xiaoying; Zhang, Bo; Xiao, Gengfu; Wang, Wei
title: RNA Interference Screening Reveals Requirement for Platelet-Derived Growth Factor Receptor Beta in Japanese Encephalitis Virus Infection
date: 2021-05-18
journal: nan
DOI: 10.1128/aac.00113-21
sha: 5356163dd5405614950263aa1397038153c94fe8
doc_id: 23107
cord_uid: zbysyonv

Mosquito-borne Japanese encephalitis virus (JEV) causes serious illness worldwide and is associated with high morbidity and mortality. To identify potential host therapeutic targets, a high-throughput receptor tyrosine kinase small interfering RNA library screening was performed with recombinant JEV particles. Platelet-derived growth factor receptor beta (PDGFRβ) was identified as a hit after two rounds of screening. Knockdown of PDGFRβ blocked JEV infection and transcomplementation of PDGFRβ could partly restore its infectivity. The PDGFRβ inhibitor imatinib, which has been approved for the treatment of malignant metastatic cancer, protected mice against JEV-induced lethality by decreasing the viral load in the brain while abrogating the histopathological changes associated with JEV infection. These findings demonstrated that PDGFRβ is important in viral infection and provided evidence for the potential to develop imatinib as a therapeutic intervention against JEV infection.

and RTK inhibitors block multiple steps of the virus life cycle (15) (16) (17) . Using an RTK RNA interference (RNAi) screen library, we identified that platelet-derived growth factor receptor beta (PDGFRb) acted as a proviral gene in JEV infection. Moreover, imatinib, a specific PDGFRb inhibitor, could robustly inhibit JEV infection both in vitro and in vivo. These results contribute to our understanding of the biology of virus entry and potentially provide new host targets for therapeutic intervention.

RTK RNAi library screen identifies PDGFRb as a pro-JEV infection gene. Arrays of four independent small interfering RNAs (siRNAs) targeting 56 RTK genes grouped in a 2 by 2 mix format were transfected into HeLa cells. Forty-eight hours after transfection, the cells were infected with recombinant JEV particles, which were packaged with the structural C, prM, and E proteins and contained a JEV luciferase-reporting replicon (18) . Twenty-four hours after infection, the cell lysates were subjected to luciferase assay (Fig. 1A) . After the primary screening, eight hits with more than 50% reduction in luciferase activity in both composition pools were selected (Fig. 1B) . The synthesized siRNAs with different sequences targeting the eight hits were tested to confirm the primary screening. Only PDGFRb was validated because four synthesized siRNAs in the secondary screen decreased the infectivity to less than 50% (Fig. 1C ). The relatively low 12.5% validation rate was due to the exclusion of invalidated siRNAs in secondary analyses and the ruling out of low gene expression with high cellular background qPCR cycle threshold (C t ; .30) values. Among the eight PDGFRb siRNAs, those that diminished the PDGFRb RNA levels inhibited recombinant JEV infection, whereas siRNAs that did not decrease the RNA levels had no effect on infection (Fig. 1C) .

PDGFRb is important in JEV infection. To verify the results obtained by the luciferase reporter assays, we investigated the effect of PDGFRb siRNA on authentic virulent JEV AT31 and SA14 strains and the attenuated SA14-14-2 strain. The inhibitory effects were investigated at RNA, protein, and virus production levels using qPCR, Western blotting (WB), and plaque assays, respectively. As expected, sharp decreases in RNA levels of both the virulent and attenuated JEV strains were detected ( Fig. 2A, D, and G) . Similarly, expression of the viral nonstructural NS3 protein was inhibited by the knockdown of PDGFRb in all the tested JEV strains (Fig. 2B, E, and H) . Intriguingly, the reduction in viral titers was approximately 2 to 3 log units in the JEV AT31 strain (Fig. 2C) , and an approximately 1-log-unit decrease was found in the SA14 strain (Fig. 2F) , whereas no obvious reduction was detected in the attenuated SA14-14-2 strain (Fig.  2I) . Overall, the results presented in Fig. 2 confirmed that PDGFRb played a critical role in JEV infection and that knockdown of PDGFRb inhibited JEV infection in vitro.

The effect of PDGFRb was further confirmed using CRISPR/Cas9 gene editing by generating a DPDGFRb single-cell clone in HeLa cells and by confirming gene deletion and cell viability ( Fig. 3A and B) . Notably, infections with both JEV AT31 and SA14-14-2 were reduced in DPDGFRb cells, suggesting that both the virulent and attenuated JEV strains were sensitive to PDGFRb (Fig. 3C to E). Moreover, transcomplementation of PDGFRb in DPDGFRb HeLa cells restored infectivity in a dose-dependent manner. As plasmid DNA can stimulate proteins associated with cGAS-STING antiviral signaling, including type I interferons (IFNs) (19) , the knockout (KO) cells were transfected with the empty vector as a control. The plasmid vector exerted limited effects on JEV infection in KO cells (Fig. 3F) .

Imatinib blocks JEV infection in vitro. Imatinib is a tyrosine kinase inhibitor that specifically targets the kinase activity of PDGFRb, ABL, and c-KIT and has been approved for the treatment of chronic myeloid leukemia and gastrointestinal stromal tumors (20-24). As PDGFRb is important in JEV infection, we further tested whether imatinib could inhibit JEV infection. Four cell types were used to evaluate the antiviral Imatinib inhibits JEV infection in vivo. As imatinib exhibited a robust inhibitory effect on JEV infection, we further examined the protective effect of imatinib against JEV-induced lethality in a mouse model. As expected, JEV-infected mice began to show symptoms, including limb paralysis, restriction of movement, piloerection, body stiffening, and whole-body tremor, from day 3 postinfection. Within 21 days postinfection, eight mice in the JEV-infected group (n = 10) succumbed to the infection, with the mortality rate being 80%, whereas imatinib treatment delayed the disease onset and reduced the mortality rate to 10% (n = 10) (Fig. 5A) . Moreover, mice in the imatinib-treated group showed slightly abnormal behavior, similar to the findings for the mice in the imatinib alone group. These results indicated that imatinib provided effective protection against JEV-induced mortality.

To further relate these protective effects to the viral load and histopathological changes in the mouse brains, the viral titer was determined and mouse brain sections were collected and assayed at day 5 postinfection. As shown in Fig. 5B , imatinib treatment significantly reduced the viral load in infected mice compared to that in infected mice with no treatment (P = 0.0032), and no plaques formed in the imatinib group (Fig.  5B) . Similarly, apparent damage to the brain, including meningitis, perivascular cuffing, vacuolar degeneration, and glial nodules, was observed in the JEV-infected group on day 5 postinfection, while imatinib treatment remarkably alleviated these phenomena (Fig. 5C ). Immunohistochemical (IHC) analysis revealed diffuse and coalescing prMstaining density in neurons in the JEV-infected group, whereas it was absent in the imatinib-treated group. These results indicated that the alleviation of histopathological changes was accompanied by a reduction in the viral load as well as a reduction in the rate of mortality, further confirming the potential curative effects of imatinib on viral encephalitis.

As JEV was rapidly cleared from the blood after inoculation and was present in the lymphatic system during the preclinical phase (25) (26) (27) (28) , the effects of imatinib on infection of the brain, blood, and spleen were evaluated at earlier time points (day 1 and 3 postinfection) to detect whether the drug reduced the peripheral viral loads. As shown in Fig. 5D to E, imatinib had little effect on peripheral JEV infection, which confirmed that imatinib protected the mice against JEV-induced lethality by reducing the viral load in the brain.

RTKs are high-affinity cell surface receptors for many polypeptide growth factors, cytokines, and hormones (29, 30) . Generally, ligand binding activates RTKs by inducing receptor dimerization and autophosphorylation of their own kinase domains, thus leading to the activation of intracellular signaling networks (31, 32) . Several RTKs have been reported to play essential roles in viral infection. Among these, the TAM subfamily (Tyro3, Axl, and Mertk) has been postulated to be an entry receptor for flaviviruses (33, 34) . However, it was recently reported that TAM is dispensable for ZIKV infection, as ZIKV was able to infect and replicate in TAM receptor knockout (KO) mice (35) . Intriguingly, WNV and La Crosse virus infections of neurons can be promoted in mice lacking Axl and Mertk (36) . Similarly, the neuroinvasion of JEV was enhanced in mice lacking Axl (37) . In this study, we attempted to identify the critical RTK molecules involved in JEV infection. In the first siRNA library screening, knockdown of either Tyro3 or Axl led to mild reduction of recombinant JEV infection with inhibition of ,50%, whereas knockdown of Mertk slightly promoted recombinant JEV infection. Among the eight primary hits, only PDGFRb was validated with additional siRNAs. Notably, screening was carried out on cell-based high-throughout screening and validation, which might be different from natural infection in vivo. As described above, the absence of Axl and Mertk would increase blood-brain barrier permeability, thus enhancing the infectivity of WNV (36) . Similarly, deficiency of Axl enhances the production of interleukin 1a (IL-1a) and thus accelerates the neuroinvasion of JEV (37) . It is impossible to establish PDGFRb KO mice because deletion of this gene is lethal (38) . Whether PDGFRb serves as a potential receptor of JEV or PDGFRb recruits the intracellular signal network to act as a proviral/antiviral protein, or whether the contribution of PDGFRb to inflammation affects the infectivity of JEV, needs to be further investigated.

However, the validation of PDGFRb still provides a promising target for the development of anti-JEV therapy. To this end, we tested the efficacy of imatinib against JEV infection both in vitro and in vivo. The pharmacokinetic and pharmacodynamic parameters of imatinib have been well characterized (39) . The maximum plasma concentrations (C max ) of imatinib at steady state in patients with gastrointestinal stromal tumors (GISTs) and chronic myelogenous leukemia (CML) have been identified as 2.9 mg/ml (4.1 mM) and 2.3 mg/ml (3.2 mM), respectively (22, 40) , which was comparable to the IC 50 reported in this study. It has been reported that intraperitoneal (i.p.) administration of 50 mg/kg/day imatinib to mice for 22 consecutive days would lead to local toxicity at the i.p. injection site, whereas little organ toxicity was observed (41) . Based on our experience, when repurposing a drug used to treat chronic diseases to combat infectious diseases, it is generally necessary to raise the drug dose to an extremely high level (27, 28, 42, 43) . Intriguingly, the dose used in this in vivo study (30 mg/kg/day, i.p.) was relatively close to the dose used in the clinic for the treatment of GIST (400 to 600 mg/day, orally [p.o.]) and CML (400 to 800 mg/day, p.o.) (21, 37) , suggesting that imatinib may be a potential safe treatment for JEV infection. Our findings that PDGFRb is important for JEV infection and that the approved drug imatinib blocks the infection suggest that an effective repurposing of PDGFRb inhibitor is a possible treatment strategy for JEV infection. JEV AT31 and SA14 strains were generated using the infectious clones of pMWJEAT-AT31 (kindly provided by T. Wakita, Tokyo Metropolitan Institute for Neuroscience) and pACYC-JEV-SA14 (GenBank accession number U14163), respectively, as previously described (18) . Briefly, the infectious clone plasmids were linearized, subjected to in vitro transcription, and delivered to BHK-21 cells via electroporation. Three days later, the supernatant was collected, propagated, and titrated in BHK-21 cells. The SA14-14-2 strain is a commercial vaccine obtained from Keqian Biology (Wuhan, China). JEV recombinant replicon particles were generated as previously described (3) . Briefly, the JEV luciferase-reporting replicon (SA14/U14163-replicon) was linearized, subjected to in vitro transcription, and delivered into BHK-21 cells via electroporation. After 72 h, the cells were transfected with pCAGGS-CprME, and the supernatant was collected 48 h later.

RTK siRNA library screening. The RTK RNAi library contained siRNAs targeting 56 human RTK genes (Qiagen, Dusseldorf, Germany), which included four different pairs of siRNAs for each gene, adding up to 226 pairs of siRNAs in total. Two by two pooled siRNAs were transfected into preseeded cells. Fortyeight hours later, the cells were infected with recombinant JEV particles. The cell lysates were subjected to luciferase activity testing (Promega, Madison, WI, USA) 24 h later. Primary hits were identified as those exhibiting a more than 50% decrease in luciferase activity relative to that of the control in the two different composition pools. Additional PDGFRb siRNAs (Table 1 , synthesized by Gene Pharma, Suzhou, China) were used for knockdown assays with recombinant JEV particles.

Cell viability. CellTiter-Lumi luminescent cell viability assay kit (Beyotime, Shanghai, China) was used to evaluate the cell viability of the KO cell line. Cell counting kit-8 (CCK-8) (GlpBio Technology, Montclair, CA, USA) assay was carried out to evaluate the effect of imatinib on cell viability. Briefly, imatinib at the indicated concentrations was added to preseeded BHK-21, Vero, HeLa, and Huh-7 cells in 96-well plates. Twenty-four hours later, cell viability was measured using the CCK-8 kit, and the light absorption value was read at 450 nm.

Antiviral assay. Cells in 96-well plates were infected with JEV AT31 (MOI: 0.1) for 1 h. Imatinib at the indicated concentrations was added to the cells from 1 h preinfection to 23 h postinfection. The antiviral effects of imatinib were evaluated using an Operetta high-content imaging system (PerkinElmer) (28) . Briefly, cells were fixed with 4% paraformaldehyde. Cells were then permeabilized using phosphate-buffered saline (PBS) with 0.2% Triton X-100 for 15 min and blocked with 5% FBS (Gibco), followed by treatment with the primary anti-JEV prM antibody (3) Imatinib administration to JEV-infected mice. All animal experimental procedures were carried out according to ethical guidelines and were approved by the Animal Care Committee of the Wuhan Institute of Virology (permit number, WIVA25201901).

Adult C3H/He female mice (4 weeks old) (45, 46) were randomly divided into three groups (30 to 36 mice each): JEV-infected, imatinib treatment, and imatinib alone. Mice in the JEV-infected group were administered i.p. injection with 10 7 PFU of JEV strain AT31 in 100 ml PBS, those in the imatinib group were treated with 30 mg/kg imatinib once a day for 21 consecutive days, and those in the imatinibtreated group were treated with 10 7 PFU of JEV strain AT31 on the first day along with 30 mg/kg imatinib once a day for 21 consecutive days. Ten mice in each group were monitored daily to assess behavior and mortality. The remaining mice were sacrificed on days 1, 3, 5, and 21 postinfection, and the brain, liver, and spleen were harvested for analysis.

To detect the viral burden using plaque assay, brain tissues were dissected and ground with 300 ml PBS, and the supernatants containing virus particles after centrifugation were serially diluted 10-fold prior to infecting BHK-21 cells. Viral titers were assessed per gram of tissue using a plaque assay.

To detect the viral burden by qPCR, tissue samples and blood were extracted with the RNAprep pure tissue kit (catalog number DP431; Tiangen, Beijing, China) and RNAprep pure blood kit (Tiangen; catalog number DP433), respectively. The viral burden was calculated on a standard curve produced using serial 10-fold dilutions of plasmids carrying the infectious clone.

For histopathological analysis, brain samples were sectioned and stained with hematoxylin and eosin (Goodbio Technology Co., Wuhan, China). For IHC staining, sections were incubated sequentially with primary anti-JEV prM antibodies (dilution, 1:200) and HRP-conjugated secondary antibodies. Additionally, 3,39-diaminobenzidine (DAB) was used for color development. Pathological changes and IHC staining were analyzed using the Pannoramic Viewer Plus software (3DHISTECH, Budapest, Hungary).

Statistical analysis. Statistical analysis was performed using GraphPad Prism 8 software (GraphPad Inc., La Jolla, CA, USA). Survival data were analyzed using the log-rank test and all other statistical analyses were assessed with the Student's t test.

We thank the Center for Instrumental Analysis and Metrology and Core Facility and Technical Support, Wuhan Institute of Virology, for providing technical assistance. 

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