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JC, QL and YW designed and performed the experiments. JZ, WX, CC and ZW provided technical assistance. JC, HY, QL and YW wrote the manuscript. JC and HY supervised the entire project.
Type I interferon (IFN) serves as the first line of defense against invading pathogens. Inhibition of IFN-triggered signaling cascade by Zika virus (ZIKV) plays a critical role for ZIKV to evade antiviral responses from host cells. Here we demonstrate that ZIKV nonstructural proteins NS1, NS4B and NS2B3 inhibit the induction of IFN and downstream IFN-stimulated genes through diverse strategies. NS1 and NS4B of ZIKV inhibit IFNβ signaling at TANK-binding kinase 1 level, whereas NS2B-NS3 of ZIKV impairs JAK–STAT signaling pathway by degrading Jak1 and reduces virus-induced apoptotic cell death. Furthermore, co-operation of NS1, NS4B and NS2B3 further enhances viral infection by blocking IFN-induced autophagic degradation of NS2B3. Hence, our study reveals a novel antagonistic system employing multiple ZIKV nonstructural proteins in restricting the innate antiviral responses.
Zika virus (ZIKV), an arbovirus belonging to the Flaviviridae family, was initially isolated from a rhesus monkey in Uganda as early as 1947 . ZIKV infection was previously thought to be asymptomatic, or to cause a mild, flu-like illness . However, ZIKV caught people’s attention during the current wide-spread epidemic in the south Pacific, and south and central America with millions of people infected [3, 4]. Mounting evidence has linked ZIKV infection to serious complications, such as the neurological autoimmune disorder Guillain–Barré syndrome and microcephaly in the newborns of mothers infected during pregnancy [5–7]. In particular, ZIKV was observed to cross the placental barrier to infect human embryonic cortical neural progenitor cells, thus disrupting brain development [8, 9]. Recently, the ZIKV infection has been shown to damage the mouse testes, posing a potential threat to mammalian reproductive system . However, there are no clinically proved vaccines or drugs available to treat ZIKV infection. Hence, there is a pressing need for comprehensive understanding of the molecular pathogenesis of ZIKV to aid in the development of effective vaccines and antiviral therapies.
As an early response to viral infection, type I interferon (IFN) produced by mammalian cells exerts antiviral activity . Activation of IFN signaling initiates from the recognition of pathogen-associated molecular patterns by different pattern recognition receptors . RIG-I-like receptors (RLRs), which recognize cytosolic viral RNA , have emerged as critical sensors for RNA viruses, including ZIKV . The binding of viral RNA triggers conformation changes of RIG-I that exposes its CARD domains for subsequent interaction with mitochondrial antiviral signaling adapter (MAVS) . This in turn allows the recruitment of TANK-binding kinase 1 (TBK1) to the signalosome and phosphorylation of interferon regulatory factor 3 (IRF3) to initiate type I IFN transcriptions . After binding to two IFN receptor subunits (IFNAR1 and IFNAR2), type I IFN transduces the signal through the Janus kinases (Jak1 and Tyk2) and signal transducers of transcription (STAT1 and STAT2), leading to the induction of various IFN-stimulated genes (ISGs), which establishes the antiviral state of the cells .
Recent studies have indicated that several ISGs, such as IFITM1 and IFITM3, can inhibit ZIKV replication . As viruses have co-evolved with hosts, they have gained multiple mechanisms to evade and antagonize host immune responses . The single-stranded positive RNA genome of flaviviruses encodes a polyprotein, which can be processed into three structural (C, prM and E) and seven nonstructural (NS1, NS2A, NS2B, NS3, NS4A, NS4B and NS5) proteins . The nonstructural proteins of flaviviruses have been implicated to be engaged in immune pathogenesis and antagonism [14, 20]. Particularly, the NS5 of ZIKV has recently been reported to target STAT2 for degradation, thus inhibiting type I IFN signaling [21, 22]. However, the roles of the orchestration of ZIKV nonstructural proteins in repressing antiviral immunity are still largely unknown. Here we report that NS1 and NS4B proteins of ZIKV could inhibit type I IFN production at TBK1 level, whereas NS2B-NS3 (NS2B3 for short) inhibited the JAK–STAT signaling downstream of type I IFN by promoting the degradation of Jak1. Meanwhile, NS2B3 also functioned as an inhibitor of virus-induced apoptosis, which may further help virus replication. Interestingly, we found that, although type I IFN restricted ZIKV replication by promoting the autophagic degradation of NS2B3, NS1 and NS4B inhibited type I IFN production to stabilize NS2B3 during viral infection. Taken together, our findings reveal a synergistic effect of NS1, NS4B and NS2B3 of ZIKV in restricting cellular antiviral responses at multiple levels.
Although neural cells are primary hosts for ZIKV, it has been proved that other cell types, such as HeLa and A549 cells, are also permissive for ZIKV [17, 23]. To investigate the role of type I IFN during ZIKV infection, A549 cells were infected with ZIKV (UG MR766 strain). The IFNβ and its downstream ISGs, including IFIT1 and IFIT2, were induced by ZIKV infection (Figure 1a and b). We also assessed the dynamic change of type I IFN in other cell lines, such as HeLa and brain cancer cell lines. The expression of IFNβ and ISGs showed the similar pattern as in A549 cells (Supplementary Figure S1A). As we found that the IFNβ expression induced by ZIKV was relatively low compared with other viruses (Supplementary Figure S1B), we hypothesized that ZIKV would inhibit type I IFN production via unidentified mechanisms. There are seven nonstructural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B and NS5) of ZIKV (Figure 1c). To investigate the roles of nonstructural proteins in IFN antiviral response, we examined the function of these nonstructural proteins in type I IFN signaling. NS1, NS2B3, NS4B and NS5 significantly inhibited IFIT2 expression after Sendai virus (SeV) infection (Supplementary Figure S1C). NS5 of ZIKV has been identified to inhibit type I IFN signaling by degrading STAT2 [21, 22]. Besides NS5, NS1 and NS4B of flavivirus are related to immune pathogenesis and NS3 is a protease crucial for the cleavage of viral proteins with the help of NS2B . So we sought to identify the roles of NS1, NS2B3 and NS4B in the regulation of type I IFN signaling pathway. Overexpression of NS1 or NS4B alone but not NS2B3 inhibited cytoplasmic poly (I:C), poly (dA:dT) as well as SeV-induced IFNβ reporter activation in 293T cells (Figure 1d–f). These results suggest that NS1 and NS4B of ZIKV may evade antiviral immunity by directly blocking type I IFN production.
We then checked how NS1 and NS4B affect type I IFN signaling, and found that both NS1 and NS4B suppressed ISRE-luc and NF-κB-luc activities induced by the two CARD domains of RIG-I (2CARD), MDA5, MAVS, TBK1 and IKKi, but not the active form of IRF3 (IRF3(5D); Figure 2a–d). To further determine whether NS1 and NS4B negatively regulate type I IFN signaling, we established a doxycycline-inducible NS1 or NS4B A549 cell lines using the TetON system. Overexpression of NS1 or NS4B restrained the phosphorylation of TBK1 and IRF3 after SeV infection (Figure 2e). The phosphorylation of p65 and degradation of IκBα were also inhibited by overexpressing NS1 and NS4B (Supplementary Figure S2A and B). Furthermore, the expressions of IFNβ and ISGs after SeV infection were also inhibited by NS1 and NS4B as expected (Figure 2f; Supplementary Figure S2C and D). We next sought to further investigate how NS1 and NS4B inhibit TBK1 phosphorylation. Co-immunoprecipitation analysis indicated that NS1 and NS4B interacted with TBK1 and blocked TBK1 oligomerization (Figure 2g and h). These results suggest that NS1 and NS4B of ZIKV are inhibitors of RLR-induced IFNβ production by targeting TBK1.
Besides antagonizing the production of IFNβ, several flaviviruses were also reported to prevent the induction of antiviral ISGs by targeting the JAK–STAT signaling pathway [24–26]. We next evaluated ZIKV’s effects on IFNAR signaling pathway. As expected, the replication of ZIKV markedly inhibited the mRNA abundance of IFN-stimulated cytokines including ISG15, IFIT1 and IFIT2 in response to IFN treatment (Figure 3a). We found that ZIKV infection induced weak activation of Jak1 and STAT1, and reduced the phosphorylation of Jak1 and STAT1 after IFNβ stimulation (Figure 3b). In addition, ZIKV infection also reduced IFNβ-induced nuclear translocation of STAT1 (Figure 3c). Interestingly, we found that ZIKV infection only reduced the protein level of Jak1 but not STAT1 (Figure 3b), while it had little effect on the mRNA level of Jak1 (Figure 3b). Taken together, our results suggest that ZIKV may block IFN-induced signaling cascade by promoting the degradation of Jak1 protein. In addition, during ZIKV infection, accumulation of ZIKV could enhance its ability to restrict the induction of ISGs at later stage of viral infection (Supplementary Figure S3A), suggesting the possibility that the enrichment of ZIKV nonstructural proteins interfered with the induction of IFN-mediated antiviral program. Using immunoprecipitation assays, we found that ZIKV NS2B3 can interact with endogenous Jak1 (Figure 3d). Moreover, the expression of ISGs such as ISG15, IFIT1, IFIT2 and Viperin was decreased in NS2B3 overexpression cells upon the stimulation of IFNβ (Figure 3e). Furthermore, overexpression of NS2B3 markedly reduced the protein levels of Jak1 but not the levels of STAT1, which consequently inhibited the phosphorylation of Jak1 and STAT1 (Figure 3f), as well as the translocation of STAT1 from the cytoplasm to the nucleus after viral infection (Figure 3g; Supplementary Figure S3B). The degradation of Jak1 can be restored by proteasome inhibitor MG132, suggesting that proteasomal degradation pathway is involved in this process (Figure 3h). The helicase domain of NS2B3 was responsible for the degradation of Jak1 as well as the inhibition of ISGs expression induced by IFNβ and SeV (Figure 3i; Supplementary Figure S3C). In general, we concluded that ZIKV was likely to suppress JAK–STAT signaling by degrading Jak1 through NS2B3.
Programmed cell death such as apoptosis is an integral part of host defensing of invading viruses, which helps to restrain the viral proliferation, and is strongly correlated to IFN signaling . The activation of RLRs can also trigger host cell apoptosis . We next wondered whether ZIKV would affect the apoptosis to assist its replication. We observed that trypan blue-positive HT1080 cells (dead cells) did not increase significantly 24 and 48h post ZIKV infection (Figure 4a), indicating the potential inhibitory functions of ZIKV on apoptotic cell death. ZIKV barely induced the cleavage of caspase 3 and poly ADP ribose polymeraze (PARP) after viral infection (Figure 4b). Furthermore, we found that the cleavage of caspase 3 and PARP induced by cytoplasmic poly (I:C) markedly decreased in the cells, which were pre-infected by ZIKV (Figure 4b). Consistently, cytoplasmic poly (I:C)-induced cell death was inhibited after ZIKV pre-infection (Supplementary Figure S4A). Next, we assessed the functions of NS1, NS2B3 and NS4B in this process. Overexpression of NS2B3, but not NS1 or NS4B, inhibited the IC poly (I:C)-induced cleavage of caspase 3 and PARP (Figure 4c). Consistently, we found that cells overexpressed with NS2B3 were more resistant to cytoplasmic poly (I:C)-induced cell death evidenced by both photographing and trypan blue staining (Figure 4d). This result was further confirmed by Annexin V/propidium iodide staining (Figure 4e). To further investigate whether NS2B3-mediated inhibition of apoptosis is related to NS2B3-mediated degradation of Jak1, we knocked down Jak1 in HT1080 cells and found the cleavage of PARP can still be inhibited by NS2B3 in Jak1 knockdown cells, indicating that NS2B3 inhibits apoptosis in a Jak1-independent manner (Supplementary Figure S4B). Taken together, these data suggest that the NS2B3 of ZIKV attenuates RLR-induced apoptosis.
To better understand the association between ZIKV infection and type I IFN signaling, we set to investigate whether type I IFN restricts ZIKV infection. After IFNβ pretreatment for half an hour, A549 cells were infected with ZIKV. As expected, pretreatment with type I IFN resulted in a marked decrease in the RNA abundance of ZIKV (Figure 5a). Subsequent experiment also showed that IFNβ treatment could promote the degradation of ZIKV NS2B3 but not alter its mRNA level (Figure 5b). As most virus infection including ZIKV resulted in the secretion of IFN, we also determined the expression levels of NS2B3 during SeV infection. Similar with the result of IFNβ treatment, SeV infection can also promote the degradation of NS2B3 (Supplementary Figure S5A). To distinguish the degradation system responsible for the IFN-induced degradation of NS2B3, we treated NS2B3-overexpressing cells with IFN in the presence of proteasome inhibitor MG132 or autophagy inhibitor Bafilomycin A1. We found that IFNβ failed to degrade NS2B3 with the treatment of Bafilomycin A1 rather than MG132 (Figure 5c). Meanwhile, the early-stage autophagy inhibitor 3-methyladenine also blocked the degradation of NS2B3 (Supplementary Figure S5B). Furthermore, IFNβ failed to degrade NS2B3 in Beclin-1 knockout cells, in which the autophagy process is deficient (Figure 5d). Confocal microscopy analysis revealed that the co-localization of NS2B3 and LC3 was enhanced after IFNβ treatment (Supplementary Figure S5C). These results suggest that IFNβ could promote autophagic degradation of NS2B3. Moreover, the degradation of NS2B3 was also in a STAT1-dependent manner (Supplementary Figure S5D). As autophagic cargo receptors are essential for delivering cargoes to the autophagosome for degradation , we next investigated which cargo receptors mediate the delivery of NS2B3 to autolysosome. We found that NS2B3 mainly interacted with p62 rather than other receptors (Figure 5e). As ubiquitin chains serve as the major recognition signal for p62-mediated selective autophagic degradation , we next confirmed that IFNβ dynamically promoted the ubiquitination of NS2B3 as well as the interaction between NS2B3 and p62 (Figure 5f and g). In addition, IFNβ failed to degrade NS2B3 in p62 knockout cells (Figure 5h). Taken together, these results indicated that IFNβ restricted ZIKV replication and promoted the autophagic degradation of NS2B3 in a p62-dependent manner.
Presuming the negative function of ZIKV NS1 and NS4B against IFN production, we speculated whether NS2B3, NS1 and NS4B might co-operate to antagonize virus-triggered IFN immunity. To confirm this hypothesis, we co-transfected these nonstructural proteins in 293T cells followed with SeV infection. As a result, NS2B3 did not affect the inhibitory function of NS1 and NS4B on IFNβ activation (Figure 6a). However, NS1 and NS4B enhanced the inhibitory function of NS2B3 on the induction of several ISGs, including IFIT1, IFIT2, MX1, ISG15 and RIG-I after SeV infection (Figure 6b). To clarify the link between attenuated IFN immunity mediated by ZIKV nonstructural proteins and antiviral response, we also monitored mRNA levels of SeV to quantify the viral replication. 293T cells co-expressing NS2B3 and NS1 as well as NS4B resulted in higher RNA levels of SeV than those only overexpressing NS2B3 or NS1/NS4B alone (Figure 6c). The results were further confirmed by plaque assay after VSV infection. Co-expressing of NS2B3, NS1 and NS4B together resulted in higher VSV titers in supernatants (Figure 6d). These results suggested co-expression of different ZIKV nonstructural proteins rendered the cells more susceptible to viral infection. To determine the mechanism of these findings, we also assessed the SeV-triggered degradation of NS2B3 in NS1 or NS4B co-expressing cells. Interestingly, NS1 or NS4B markedly impaired SeV-induced degradation of NS2B3 (Figure 6e). Collectively, the co-operation between ZIKV NS2B3, NS1 and NS4B further prevents the induction of antiviral ISGs during viral infection, which benefits ZIKV by evading the IFN immune response.
There is no doubt that co-evolution between flaviviruses and their hosts has taken place over a long period of time. Host cells have developed multiple branches of innate immune system to keep the virus invasion and replication under control . Previously, several groups have demonstrated the importance of IFN pathway in restricting different flaviviruses from invasion to replication [14, 31]. Although many studies have reported ISGs such as IFITM family can inhibit the replication of ZIKV , little is known about the relationship between host IFN system and ZIKV replication. Here we show that IFNβ restricts replication of ZIKV and promotes autophagic degradation of NS2B3, which broadens our understanding of the host innate immune protective defense against ZIKV. As the ubiquitination of NS2B3 is enhanced by IFN-β treatment and STAT1 is required for the degradation of NS2B3, the potential IFN-inducible E3 ligases might be involved in this process. Many E3 ligases such as tripartite motif (TRIM) proteins family members, including TRIM5α, TRIM23, TRIM25 and TRIM31, can be upregulated by IFN through STAT1 [32, 33]. Most of these TRIM proteins play critical roles in antiviral responses as well as the host restriction on viral replication [33–37]. In this case, further studies are needed to investigate their functions on NS2B3 ubiquitination as well as degradation.
It has been well documented that different flaviviruses have developed diverse strategies to minimize induction of IFN . Previous studies have identified several strategies for ZIKV to evade the innate immune system. For example, ZIKV NS5 protein could inhibit type I IFN pathway by targeting STAT2 . Here we screened the function of ZIKV nonstructural proteins and showed that they are committed to thwarting the host innate immune response through diverse mechanisms. NS1 and NS4B of ZIKV prevent the activation of RLR-triggered type I IFN induction pathway by targeting TBK1 and subsequently inhibit the synthesis of IFNs. Unlike NS1 and NS4B of ZIKV, NS2B3 does not affect type I IFN production, but impairs JAK–STAT signaling pathway through degrading the tyrosine-protein kinase Jak1 in a proteasome-dependent manner, hence reducing the phosphorylation levels of Jak1 and STAT1. Although the inhibition of ISG expressions may have some feedback effects on IFN production at the later stage of infection in vivo, the effects may vary among different cell types, and they may not be strong enough for the feedback effects of JAK–STAT signaling to affect RIG-I signaling in 293T cells, which possibly accounts for the finding that NS2B3 cannot directly inhibit IFNβ activation in our system. NS2B3 also attenuates RLR-induced apoptotic cell death to ensure the complement of viral cell life cycle (Figure 7). It has been noticed that ZIKV could induce apoptosis of neural progenitor cells [38, 39], so we speculated that ZIKV may distinctively regulate apoptosis signaling in different cells upon different stimulations. Further investigations are required to reveal its detail mechanisms in different cell types.
Until now, most studies about flaviruses infection have focused on delineating the function of single nonstructural protein in the antiviral immunity . Here we show that ZIKV nonstructural proteins NS1 and NS4B inhibit the autophagic degradation of NS2B3, thus work collaboratively to minimize the antiviral immunity. Collaborative effort between multiple viral nonstructural proteins should be given more emphasis and attention during elucidating the mechanism of ZIKV infection.
Taken together, we found that multiple nonstructural proteins of ZIKV negatively modulated antiviral response at various levels by inhibiting type I IFN production and the expression of downstream ISGs. Our findings provide evidence to support the potential synergy between ZIKV nonstructural proteins to build up the antagonistic system against innate antiviral immunity, and shed new light on ZIKV immune evading mechanism to suggest novel targets for developing rational vaccine strategies.
HEK293T, A549, HT1080, HeLa, LN229, U87 and U251 cells were cultured in Dulbecco’s modified Eagle medium (Corning, Manassas, VA, USA) with 10% fetal bovine serum (Genstar, Beijing, China) in a 5% CO2 incubator at 37°C. Recombinant human IFNβ was purchased from Peprotech (Rocky Hill, NJ, USA). Poly (I:C) (LMW) and poly (dA:dT) were purchased from Invivogen (San Diego, CA, USA). Doxycycline (D9891), MG132 (C-2211-5MG), Bafilomycin A1 (H2714) and 3-methyladenine (M9281-100MG) were purchase from Sigma (Shanghai, China).
Cells were either mock-infected or infected with ZIKV (UG MR766 strain), which was kindly provided by Dr Gucheng Zeng, Sun Yat-sen University. Virus was allowed to adsorb at room temperature for 1h before incubation at 37°C for indicated time as previously described . Plaque assays were performed to determine viral titer as previously described . SeV was kindly provided by Dr F Xiao-Feng Qin (Suzhou Institute of Systems Medicine). Cells were infected at different multiplicity of infection (MOI) and time points as indicated.
Plasmids encoding ZIKV NS1, NS2B3 and NS4B were chemically synthesized based on Z1106033 ZIKV strain (NCBI ID: KU312312) and sub-cloned into pcDNA3.1 expression vectors using standard molecular biology techniques. RIG-I (2CARD), MDA5, MAVS, TBK1, IRF3 (5D) and IFNβ, ISRE, NF-κB luciferase reporter plasmids have been previously described . Other plasmids mentioned were acquired by the means of standard PCR techniques. Horseradish peroxidase anti-Flag (M2; A8592) and anti-β-actin (A1978) were purchased from Sigma. Horseradish peroxidase anti-hemagglutinin (HA; 12013819001) was purchased from Roche Applied Science (Shanghai, China). Anti-pTBK1 (5483), anti-TBK1 (3013), anti-pIRF3 (4947s), anti-Jak1 (3344), anti-pJak1 (3331), anti-pSTAT1(9167), anti-C-PARP (5625), anti-C-Caspase 3 (9661), anti-p62 (8025) and anti-Beclin-1 (3738) were acquired from Cell Signaling Technology (Danvers, MA, USA). Anti-IRF3 (sc-9082) and anti-STAT1 (sc-346) were from Santa Cruz Biotechnology (Dallas, TX, USA).
For immunoprecipitation, whole-cell lysates were prepared after transfection, followed incubation overnight with the appropriate anti-Flag beads (Sigma) or anti-HA beads (Sigma). Beads were washed three to five times with low-salt lysis buffer, and immunoprecipitates were eluted with 2× SDS-loading buffer and resolved by SDS-polyacrylamide gel electrophoresis. Proteins were transferred to polyvinylidene fluoride membranes (Bio-Rad, Shanghai, China) and further incubated with appropriate antibodies. LumiGlo Chemiluminescent Substrate System (Millipore, Shanghai, China) was used for protein detection.
293T cells were transfected with a mixture of luciferase reporter (firefly luciferase), pRL-TK (renilla luciferase plasmid), an indicated variety expression plasmid or empty vector (pcDNA3.1) plasmid. Then, the cells were transfected with RIG-I (2CARD), MDA5, MAVS, TBK1 and IRF3 (5D), or stimulated with IC poly (I:C), poly (dA: dT) or infected with SeV. Luciferase activity was measured at 24h after transfection or infection using a luminometer (Thermo Scientific, Shanghai, China) with a dual-luciferase reporter assay system according to the manufacturer’s instructions (Promega, Beijing, China). Data represent relative firefly luciferase activity, normalized to renilla luciferase activity.
Total RNA was extracted using TRIzol reagent (Invitrogen, Shanghai, China) and reverse-transcribed using oligo-dT primers and reverse transcriptase (Vazyme, Nanjing, China). Quantitative real-time PCR was performed using SYBR Green qPCR Mix kit (Genstar) with primers as follows:
IFNβ: Forward: 5′- CCTACAAAGAAGCAGCAA-3′
Reverse: 5′- TCCTCAGGGATGTCAAAG-3′
ISG15: Forward: 5′- TCCTGGTGAGGAATAACAAGGG-3′
Reverse: 5′- GTCAGCCAGAACAGGTCGTC-3′
IFIT2: Forward: 5′- GGAGGGAGAAAACTCCTTGGA-3′
Reverse: 5′- GGCCAGTAGGTTGCACATTGT-3′
IFIT1: Forward: 5′- TCAGGTCAAGGATAGTCTGGAG-3′
Reverse: 5′- AGGTTGTGTATTCCCACACTGTA-3′
MX1: Forward: 5′- GTTTCCGAAGTGGACATCGCA-3′
Reverse: 5′- CTGCACAGGTTGTTCTCAGC-3′
VIPERIN: Forward: 5′- TGGGTGCTTACACCTGCTG-3′
Reverse: 5′- GAAGTGATAGTTGACGCTGGTT-3′
CCL5: Forward: 5′- GGCACGCCTCGCTGTCATCCTCA-3′
Reverse: 5′- CTTGATGTGGGCACGGGGCAGTG-3′
RIG-I: Forward: 5′- TGTTCTCAGATCCCTTGGATG-3′
Reverse: 5′- CACTGCTCACCAGATTGCAT-3′
SeV pRNA: Forward: 5′- GACGCGAGTTATGTGTTTGC-3′
Reverse: 5′- TTCCACGCTCTCTTGGATCT-3′
ZIKV genomic RNA: Forward: 5′- TTGGTCATGATACTGCTGATTGC-3′
Reverse: 5′- CCYTCCACRAAGTCYCTATTGC-3′
RPL13A: Forward: 5′- GCCATCGTGGCTAAACAGGTA-3′
Reverse: 5′- GTTGGTGTTCATCCGCTTGC-3′.
HeLa cells seeded on Glass Bottom culture dishes (Nest Scientific, Jiangsu, China) were fixed with 4% paraformaldehyde for 15min, and then permeabilized in methyl alcohol for 10min at −20°C. After washing with PBS for three times, cells were blocked in 5% fetal goat serum for 1h, and then incubated with primary antibodies diluted in 10% bull serum albumin overnight. The cells were washed, and followed by a fluorescently labeled secondary antibody (Alexa Fluor 488- and Alexa Fluor 568-conjugated antibodies against mouse, rabbit or goat IgG (Biotium, Hayward, CA, USA)). For viral infection, HeLa cells were either mock-infected or infected with ZIKV (MOI=1) for 48h following with or without IFNβ for 30min and fixed with 4% paraformaldehyde, permeablized with methyl alcohol, blocked with 5% fetal goat serum and incubated with the indicated antibodies. The images were photographed by laser scanning confocal microscope (Leica, Wetzlar, Germany).
293T cells transfected with various combinations of plasmids for NS1, NS2B3 and NS4B were infected by VSV for 18h. The virus-containing supernatants were collected. Vero cells were infected with VSV supernatants for 1h at room temperature as described . After washing with PBS, the plate was overlaid with Dulbecco’s modified Eagle medium containing 1% low melting-point agarose and incubate at 37°C for 24h before crystal violet staining.
Data are represented as mean±s.d. when indicated, and two-tailed Student’s t-test was used for statistical analysis. Differences between groups were considered significant when P-value was<0.05.
We thank Dr Gucheng Zeng for the assistance of ZIKV infection experiments. This work was supported by National Key Basic Research Program of China (2015CB859800), National Natural Science Foundation of China (31522018 and 31170832), Guangdong Natural Science Funds for Distinguished Young Scholar (S2013050014772), the Fundamental Research Funds for the Central Universities (15lgjc02), the Training Program for Outstanding Young Teachers in Higher Education institutions of Guangdong Province (YQ2015001), Guangzhou Science and Technology Project (201605030012) and National Key Research Program of China (2016YFD0500300).
(Supplementary information is linked to the online version of the paper on the Cell Discovery website.)
The authors declare no conflict of interest.