Abstract
Enterovirus A71 (EV-A71) is a human pathogen causing hand, foot, and mouth disease (HFMD) in children. Its infection can lead to severe neurological diseases or even death in some cases. While being produced in a large quantity during infection, viral proteins often require the assistance from cellular chaperones for proper folding. In this study, we found that heat shock protein A6 (HSPA6), whose function in viral life cycle is scarcely studied, was induced and functioned as a positive regulator for EV-A71 infection. Depletion of HSPA6 led to the reductions of EV-A71 viral proteins, viral RNA and virions as a result of the downregulation of internal ribosomal entry site (IRES)-mediated translation. Unlike other HSP70 isoforms such as HSPA1, HSPA8, and HSPA9, which regulate all phases of the EV-A71 life, HSPA6 was required for the IRES-mediated translation only. Unexpectedly, the importance of HSPA6 in the IRES activity could be observed in the absence of viral proteins, suggesting that HSPA6 facilitated IRES activity through cellular factor(s) instead of viral proteins. Intriguingly, the knockdown of HSPA6 also caused the reduction of luciferase activity driven by the IRES from coxsackievirus A16, echovirus 9, encephalomyocarditis virus, or hepatitis C virus, supporting that HSPA6 may assist the function of a cellular protein generally required for viral IRES activities.
Introduction
The enterovirus A71 (EV-A71) belongs to the genus Enterovirus in the family Picornaviridae. EV-A71 infection often manifests as hand, foot, and mouth disease (HFMD), but occasionally leads to life-threatening neurological complications such as aseptic meningitis, brain stem encephalitis or acute flaccid paralysis (). EV-A71 is currently considered as the most neurotropic enterovirus and a public health issue worldwide (Yi et al., 2017; ).
The RNA genome of EV-A71 is approximate 7.4 kilobases and encodes a single polyprotein. Following the steps of attaching and penetrating via receptor-mediated endocytosis, viral RNA (vRNA) of EV-A71 is released into the cytoplasm by an endosome-dependent uncoating process (; ). The genomic RNA, also functioning as the mRNA, is immediately translated into a polyprotein, which is then processed into 10 different viral proteins including viral RNA polymerase 3Dpol by viral proteases 2Apro, 3Cpro, and 3CDpro. The 3Dpol directs the synthesis of both genomic and antigenomic RNA in a membrane-associated replication complex containing viral proteins or their precursors including 2BC, 2B, 2C, 3A, and 3CDpro as well as host proteins (; ; van der Schaar et al., 2016). The newly synthesized genomic RNA is then packaged into viral particles followed by a maturation process (). Most assembled virions are released upon cell lysis as a result of the viral protein-induced apoptosis (; ); on the other hand, a small portion of the virions can be released via membrane-bound vesicles in a non-lytic manner (; ; ; ; ).
EV-A71 translation is mediated by the internal ribosome entry site (IRES) located at a highly structured 5′ untranslated region of the viral genome. The IRES-mediated translation allows viral proteins to be synthesized while host cap-dependent translation is shut off during viral infection (; ; ; ). Nevertheless, the IRES-mediated translation requires canonical translational initiation factors such as eIF4A, eIF4B, eIF3, eIF2, and eIF1A (), as well as the 2Apro-cleaved eIF4G (; ; ; ; ). In addition to canonical translational factors, several cellular IRES trans-acting factors (ITAFs) modulate IRES activity [reviewed in ]. Up to date ITAFs known to promote the activity of EV-A71 IRES include heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) (; ), poly (rC)-binding proteins 1 and 2 (PCBP1/2) (; ), polypyrimidine tract-binding protein 1 (PTBP1) (Xi et al., 2019), HuR, Ago2 (), the 68-kDa Src-associated protein in mitosis (Sam68) (Zhang et al., 2015), far-upstream element-binding protein 1 (FBP1) (), and DDX3X RNA helicase reported by us ().
When cells are exposed to stress, heat shock proteins (HSPs) are synthesized at increased level to maintain cellular homeostasis. HSP70 is a subfamily of HSP superfamily with approximate 70 kDa molecular weight, which accounts for the majority of molecular chaperones in cells (). There are at least 14 human HSP70 proteins that differ in aspects like expression level, subcellular localization, and inducibility to stress (). They can be classified into “stress-induced,” e.g., HSPA1 (aka HSP72) and HSPA6 (aka HSP70B’), and “constitutively expressed,” e.g., endoplasmic reticulum (ER)-residing HSPA5 (aka GRP78), HSPA8 (aka HSC70), and mitochondrial-residing HSPA9 (aka GRP75). HSP70 proteins, whose binding to client proteins is regulated by ATP hydrolysis, generally do not work alone but cooperate with HSP40 cochaperones (). Other than helping cells to cope with stress, HSP70s also participate positively in diverse steps of the virus replication cycle. For instances, HSPA1 facilitates replication complex formation for hepatitis C virus (HCV) (). HSPA5 assists entry and replication for Japanese encephalitis virus (JEV) () and coxsackievirus A9 (CA-V9) (). HSPA8 has roles in divergent steps during the infection of Dengue virus, Rotavirus or JEV (; Zárate et al., 2003; ). It also regulates EV-A71 IRES-mediated translation by interacting with 2Apro and promoting eIF4G cleavage (). In addition, we reported that HSPA1, HSPA8 and HSPA9 regulate multiple steps of the EV-A71 life cycle including IRES-mediated translation (). These are just few examples to demonstrate the importance of HSP70s in various steps of virus infection processes. In addition to HSP70s, HSP27 facilitates EV-A71 IRES activity by enhancing 2Apro-dependent eIF4G cleavage, a function similar to HSPA8, and hnRNP A1 cytoplasmic translocation ().
Both HSPA1 and HSPA6 (sharing 85% sequence identity) (; ) are stress-induced HSP70s. While the functions of HSPA1 in virus replication cycle have been discussed widely [reviewed in ], there is little information regarding the function of HSPA6 in viral life cycle. HSPA6 is strictly inducible, having low or non-detectable expression levels in most cells (, ), and may share overlapping functions with HSPA1 in response to cellular stresses (; ). The only report showing HSPA6 may have any role in a given virus is its association with the 3′UTR of HCV genome (); however, the meaning of this association is not clear.
In this study, we found that HSPA6 protein was induced during EV-A71 infection. Depletion of HSPA6 led to the reductions of viral proteins, viral RNA, and virion production, indicating that HSPA6 had a positive role in the EV-A71 life cycle. We investigated at which step HSPA6 was involved during EV-A71 infection and found that it was only required for the IRES-mediated translation. Unexpectedly, the negative consequence of HSPA6 depletion in the IRES-mediated translation could be observed in the absence of viral proteins, suggesting that HSPA6 acted on cellular factors to facilitate IRES activity. Alternatively, it may affect viral IRES activity by its mRNA binding activity (). Intriguingly, knockdown of HSPA6 also affected the translation directed by the IRES from coxsackievirus A16 (CV-A16), echovirus 9 virus (echo 9), encephalomyocarditis virus (EMCV), or hepatitis C virus (HCV), supporting that HSPA6 may assist the function of cellular protein(s) generally required for viral IRES activities. This is the first report functionally demonstrated that HSPA6, a novel inducible HSP70 member, impacts a viral life cycle.
Materials and Methods
Cells and Viruses
RD (Human rhabdomyosarcoma; ATCC®, CCL-136TM), HEK293T, HeLa and Huh7 cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM, Gibco) containing 100 unit/ml penicillin, 10 μg/ml streptomycin, 0.25 μg/ml amphotericin B, 2 mM L-glutamine and 10% fetal bovine serum (HyClone) at 37°C with 5% CO2. The EV-A71 genotype C strain (4643/Taiwan/1998), provided by Dr. Shin-Ru Shih (Chang-Gung University, Taiwan), was amplified in RD cells. All experiments using infectious viruses were carried out in biosafety level 2 laboratory, following the guidelines of the Center of Environmental Protection and Safety and Health (National Yang-Ming University, Taiwan).
Plasmids
The detailed construction of R1 replicon has been described previously (). Briefly, for R1 3DD330A, in which Asp330 was mutated to an Ala to disrupt the enzymatic activity, was constructed by PCR-based site-directed mutagenesis using the R1 replicon as a template (). The monocistronic reporter plasmid (IRES-Luc), which contains EV-A71 IRES at the 5′end and drives the translation of the luciferase protein, was described previously (). To construct pFlag-CMV2-HSPA6, HSPA6 gene was amplified from the cDNA of EV-A71 infected RD cells by nested PCR and then cloned into pFlag-CMV2 (Sigma-Aldrich) at NotI and KpnI sites to generate pFlag-HSPA6. A wobble HSPA6 mutation (nucleotides 7–9 GCC→GCA), which resists the action of sgRNA used in knockout cells, was generated by site-direct mutagenesis. HCV IRES-Luc was previously described (). CV-A16 IRES-Luc and Echo 9 IRES-Luc were gifts from Dr. Szu-Hao Kung (National Yang-Ming University, Taiwan) (). EMCV IRES-Luc was generated by inserting firefly Luc gene into the pTM1 plasmid (Addgene).
Antibodies
Commercial antibodies used in this study were mouse anti-EV-A71 VP1 (Abnova), mouse anti-EV-A71 VP0/VP2 (Millipore), mouse anti-HSPA6 (Enzo), sheep anti-mouse IgG conjugated to horse radish peroxidase (HRP) (GE Healthcare) and goat anti-mouse IgG (H+L) conjugated to Alexa Fluor Plus 488 (Invitrogen). The mouse antisera against EV-A71 2C, 3Cpro and 3Dpol were home made using purified recombinant 6× His-tagged proteins from Escherichia coli.
Western Blot Analysis
Cells were lysed in RIPA buffer (pH 7.4, 50 mM Tris–HCl, 150 nM NaCl, 1% NP-40, 0.1% SDS, 0.1% DOC, 2 mM EDTA, 10 mM NaF, 1 mM Na3VO4, 1 mM PMSF, 50 μM leupeptin, 50 μM aprotinin), mixed with cracking buffer (pH 6.8, 250 mM Tris–HCl, 40% glycerol, 20% β-ME, 8% SDS, 0.04% bromophenol blue), and resolved by 7.5 or 10% SDS-polyacrylamide gels. For viral protein detection, 50 μg of lysate was used, while for HSPA6 detection, 75 μg of lysate was used. Gels were then electro-transferred onto polyvinylidene difluoride membranes at 120 V for 3 h for viral proteins or 55 V for 16 h for HSPA6 (transfer buffer: 25 mM Tris, 192 mM glycine, 20% methanol). After blocked in TBS-T [50 mM Tris–HCl (pH 7.6), 150 mM NaCl, 0.1% Tween-20] containing 5% non-fat milk, the membranes were incubated with various primary antibodies. For HSPA6 detection, membrane was incubated with anti HSPA6 antibody (1:100) for 32 h, followed by incubation with secondary antibody for 16 h. Signals were detected with ECL Western blotting detection reagent.
Quantitative RT-PCR (RT-qPCR) and in vitro Transcription
Total RNA was extracted using TRizol (Invitrogen), followed by reverse transcription using Hiscript I reverse transcriptase (Bionovas). 1/12 of the total cDNA was subjected to qPCR with primers specific to 3Dpol (vRNA), GAPDH (internal control), and luciferase reporter plasmids (Supplementary Table 1 for primer sequences) using Fast SYBR Green Master Mix (Applied Biosystems). For generating in vitro transcribed RNA, plasmids IRES-Luc (XbaI), R1 3DD330A (SalI), EMCV IRES-Luc (SalI), and HCV IRES-Luc (SalI), CV-A19 IRES-Luc (ScaI), and Echo 9 IRES-Luc (ScaI), linearized by restriction enzyme specified in the parentheses, were used as templates and transcribed using MEGAscript T7 transcription kit (Invitrogen). 2 μg of the RNA was transfected into cells using Lipofectamine 3,000 reagent (Invitrogen). Cells were harvested for RT-qPCR or luciferase assay at the time point specified in each figure.
Lentivirus-Based HSPA6 Knockdown and Knockout
For HSPA6 knockdown, lentiviruses expressing HSPA6 shRNA (clone 1: GATGTGTCGGTTCTCTCCATT and clone2: GAGCAGTACAAGGCTGAGGAT) were used to infect RD cells. Puromycine (2.5 μg/ml) resistant RD cells were used for subsequent experiments. For HSPA6 knockout, CRISPR/Cas9 system for HSPA6 knockout (sgRNA: GCCCACCGCGAGCTCCCGTG) and its control were purchased from National RNAi Core Facility (Academia Sinica, Taiwan). After puromycin (2.5 μg/ml) selection, clones are amplified from single RD cell isolated by limiting dilution. To validate HSPA6 KO, cells were challenged with heat shock condition (42°C, 2 h) and collected for Western analysis using anti HSPA6 antibody (Enzo).
Virus Titration
The supernatant containing extracellular viruses was collected from the EV-A71 infected RD cell culture and centrifugated at 5,700 × g for 5 min to remove cell debris. Cell associated viruses were prepared from cell lysates collected after freeze-and-thaw cycles and centrifugation at 15,300 × g for 10 min. The infectious viral titer was measured using fifty-percent tissue culture infective dose (TCID50) according to the Reed-Muench method.
Viral Entry Detection
RD cells cultured on poly-L-Lysine coated coverslips were pretreated with 100 μg/ml cycloheximide for 1 h to prevent virus translation before viral infection, and then challenge with EV-A71 (MOI = 300) for another 1 h to allow viral internalization in the presence of cycloheximide. In the JG40 control experiment, JG40 (5 μM) was added together with cycloheximide. The cells were washed three times with PBS and fixed with ice-cold methanol for 3 min. After another PBS wash, the cells were permeabilized with 0.2% Triton X-100 at room temperature for 20 min, and then incubated with blocking buffer (5% FBS and 0.75% BSA in PBS) at room temperature for 1 h. The cells were treated with mouse antibody against EV-A71 VP0/VP2 (Millipore) at room temperature for 2 h, and stained with goat anti-mouse IgG (H + L) conjugated to Alexa Fluor Plus 488 (Invitrogen) at room temperature for 2 h. Cell nuclei were stained with 0.5 nM DAPI, prior to mounting on glass slides. The specimens were observed by confocal microscopy (ZEISS LSM 700). The signal intensity was quantified using Metamorph software.
Luciferase Reporter Assay
The detailed construction of IRES-Luc () and R1 3DD330A () were previously described. 1 μg of in vitro transcribed reporter RNA of IRES-Luc or R1 3DD330A was transfected into HSPA6 KO and knockdown RD cells. HSPA6 shRNA #2 was used for knocking down HSPA6 in the RD cells used in the luciferase assays. The cell lysates were harvested at time points indicated. 2 μg of in vitro transcribed reporter RNA of the CV-A19 IRES-Luc, Echo 9 IRES-Luc and EMCV IRES-Luc were transfected into HeLa cells; and the reporter RNA of HCV IRES-Luc was transfected into Huh7 cells. The cell lysates were harvested at 6 h post transfection. One third of cell lysates were used for luciferase activity using Bright-GloTM Luciferase assay system (Promega). One half of the cell lysates were used for RNA purification, which was subjected to RT-qPCR and then used for the normalization of transfection efficiency. Luciferase activity was normalized with RNA transfected to reflect IRES activity.
Cycloheximide Chase
To monitor the stability of viral proteins, the RD cells were treated with 100 μg/ml cycloheximide (CHX) at 9 h post EV-A71 infection, and then the cell lysates were harvested at 1, 2, 4, and 6 h post cycloheximide treatment. The equal volume of each sample was loaded into SDS-PAGE for Western blot analysis using antisera against non-structural proteins 2C, 3Cpro, and 3Dpol. The signal intensity of each band was quantified by ImageJ software and plotted as the value taken 1 h CHX treatment as 100%. The linear regression curves were charted by GraphPad Prism five software.
Statistics Analysis
All the data analyses and statistical graphs were processed by GraphPad Prism five software. The statistical methods used in this study were unpaired Student’s t-test or one-way ANOVA followed by Dunnett’s post hoc test. A P-value < 0.05 is regarded as statistically significant. (∗∗∗P < 0.001, ∗∗P < 0.01, and ∗P < 0.05).
Results
HSPA6 Is Induced to Support EV-A71 Replication Cycle
In the previous study, we have reported that HSP70 family proteins, including HSPA1, HSPA8 and HSPA9, played positive roles in EV-A71 life cycle (). Here we report that an additional HSP70 member, HSPA6, was induced and reached to a peak at 6 h post infection (hpi) (Figure 1A and Supplementary Figure 1). The HSPA6 protein induction from three biological repeats was quantified (Figure 1A). To understand the importance of this induction, we infected RD cells with a lentivirus carrying the shRNA specific to HSPA6, followed by EV-A7 infection 48 h post lentivirus transduction. While both shRNA clones (#1 and #2) reduced amount of HSPA6 mRNA and protein, shRNA #2 gave a better knockdown efficiency in RD cells (Figure 1B). Both viral RNA (vRNA) levels (Figure 1C) and viral protein production of 3Dpol and VP1 (Figure 1D) were decreased in HSPA6-depleted cells. HSPA6 depletion did not reduce cell viability (Figure 1B). Notably the reduction was proportional to the knockdown efficiency, suggesting a positive role of HSPA6 in EV-A71 life cycle.
FIGURE 1
HSPA6 Is a Positive Regulator for EV-A71 Life Cycle
Because using shRNA only achieved partial depletion of HSPA6 in RD cells (Figure 1B), we therefore generated an HSPA6 knockout (KO) RD clone using the CRISPR/Cas9 approach. HSPA6 protein production was examined among cell lysates prepared from wild-type (WT) and HSPA6 KO RD cells with or without heat treatment. While HSPA6 protein was highly induced in WT RD cells under the heat shock (HS) condition, it became undetectable in HSPA6 KO cells (Figure 2A), indicating HSPA6 was well depleted. To better understand how HSPA6 impacts EV-A71 life cycle, the levels of viral protein, vRNA and viral titer were compared between WT and HSPA6 KO RD cells infected with EV-A71. The results showed that 3Dpol and VP1 proteins were produced at ∼40% in HSPA6 KO cells as compared to those in WT cells (Figure 2B). Cell-associated viral RNA was reduced to 50% in HSPA6 KO cells as well (Figure 2C). Total virions, which included cell-associated and extracellular viral particles, were collected from 3 to 12 hpi at 3-h intervals and then titrated. The data revealed that viral production was reduced in the absence of HSPA6 protein at all-time points and with a biggest difference (∼4.8-fold) at 6 hpi (Figure 2D). Put together, these data indicate that HSPA6 has a positive role in EV-A71 life cycle.
FIGURE 2
To rule out that the reductions in viral protein, vRNA and titer were due to off-target effects of the sgRNA, we conducted rescue experiments. We transfected HSPA6 KO RD cells with a small amount of HSPA6-expressing plasmid (0.2 μg/6 × 105 cells) to restore HSPA6 expression close to its endogenous levels before EV-A71 infection (Figure 2E, compare lanes 1 and 4). The cells were harvested at 6 hpi for the analysis of viral proteins (3Dpol and VP1) and cell associated vRNA, and at 12 hpi for the measurement of total viral titers. The results indicated that ectopic HSPA6 expression in WT RD further increased 3Dpol level (Figure 2E), vRNA (Figure 2F), and viral titer (Figure 2G). More importantly, it also restored these three infection indices in HSPA6 KO RD cells (Figures 2E–G). These data demonstrated that the reduction of viral propagation in HSPA6 KO RD cells was not caused by off-target effects. Thus, we concluded that HSPA6 facilitates EV-A71 life cycle.
HSPA6 Is Not Needed for EV-A71 Internalization
We next investigated at which stage of the EV-A71 life cycle HSPA6 was involved. RD cells were pretreated with cycloheximide (CHX) for 1 h before EV-A71 infection. To study if HSPA6 plays a role in EV-A71 internalization, the CHX treated cells were then infected with EV-A71 for 1 h to allow viral particles internalization and then harvested immediately for immunofluorescence staining using antibody against EV-A71 VP0/VP2. The CHX pre-treatment prevented vRNA translation upon viral entry, therefore any VP0/VP2 signals detected would be from the entering viral particles exclusively. JG40, an EV-A71 inhibitor (), was used as a control. The images of confocal microscopy (Figure 3A) as well as their quantification data (Figure 3B) showed no significant difference in VP0/VP2 signals between WT and HSPA6 KO cells, suggesting that HSPA6 is not needed for EV-A71 entry into RD cells.
FIGURE 3
HSPA6 Is a Positive Regulator for EV-A71 IRES-Mediated Translation
The immediate step following its entry and uncoating is the translation of vRNA mediated by the IRES during EV-A71 life cycle. We first examined if RNA transfection had any impact on HSPA6 protein expression and found that HSPA6 was induced (Supplementary Figure 2). To examine the potential roles of HSPA6 in EV-A71 IRES-mediated translation, an R1 3DD330A mutant replicon (Figure 4A) was firstly used. This replicon contains a luciferase reporter replacing the P1 region of the EV-A71 genome and has a D330A mutation in the 3Dpol region. A PEST (Pro, Glu, Ser, and Thr) sequence was added at the carboxyl terminus of luciferase, which caused rapid degradation of the luciferase protein and therefore minimized protein accumulation. This allows the Luc activity measured to reflect the translational activity at the moment. In addition, the enzymatic mutation of D330A in the 3Dpol region prevents amplification of the replicon () and the lack of P1 structure protein region avoids the formation of new viral particles, thus the luciferase activity would solely reflect translational activity. The in vitro transcribed RNA of R1 3DD330A mutant replicon was transfected into knockdown control (shCtrl) and HSPA6 knockdown RD cells (Figure 4B), or WT and HSPA6 KO RD cells (Figure 4C). The luciferase activity was measured at 3, 6, 9, and 12 h post transfection and normalized with the RNA levels transfected in each cell line. The luciferase activity was significantly lower in both HSPA6 knockdown (Figure 4B) and HSPA6 KO cells (Figure 4C) at each time point as compared to that in control cells. The luciferase activity was reduced to 20 and 31% at 6 h post transfection in HSPA6 knockdown and HSPA6 KO cells, respectively. Since HSPA6 was induced during EV-A71 infection, we first examined the function of HSPA6 in IRES activity during EV-A71 infection. The in vitro transcribed RNA of IRES-Luc, which is a Luc reporter containing no additional viral genes (Figure 4D), was transfected at 6 hpi into EV-A71-infected knockdown control (shCtrl) and HSPA6 knockdown RD cells (Figure 4E), or WT and HSPA6 KO RD cells (Figure 4F). Cells were harvested for luciferase activity measurement at 3, 6, 9, and 12 h post transfection. Similarly, the luciferase activity was significantly lower in both HSPA6 knockdown (Figure 4E) and HSPA6 KO cells (Figure 4F) at each time point as compared to that in control cells. The luciferase activity was reduced to 15 and 30% at 6 h post transfection in HSPA6 knockdown and HSPA6 KO cells, respectively. These results demonstrated that HSPA6 played a positive role in EV-A71 IRES activity during infection. It is known that IRES-mediated translation of EV-A71 could be regulated by either cellular ITAFs or viral proteins (), whose folding is governed by HSP70s (). Thus, we asked whether HSPA6 could stimulate IRES activity without the presence of viral proteins. The in vitro transcribed RNA of IRES-Luc was transfected into cells without EV-A71 infection and luciferase activity was measured at 3, 6, 9, and 12 h post transfection. The results showed that in the absence of EV-A71 viral proteins, comparable patterns of reduction in IRES-mediated luciferase activity were found in both HSPA6 knockdown (Figure 4G) and HSPA6 KO cells (Figure 4H) as those in the presence of EV-A71 infection. The luciferase activity was reduced to 21 and 35% in HSPA6 knockdown and HSPA6 KO cells at 6 h post transfection, respectively, suggesting that HSPA6 possibly modulates IRES activity through regulating cellular factors rather than viral proteins.
FIGURE 4
HSPA6 Depletion Does Not Influence EV-A71 Replication Efficiency
During the infection cycle of positive sense RNA viruses including EV-A71, it is technically difficult to separate the replication period from the translation period because these two steps are tightly linked and overlapped. Depletion of HSPA6 reduced IRES-mediated translation (Figure 4), which would lead to the reduction of viral RNA synthesis naturally due to the decrease in viral protein production. As a consequence, we were unable to determine if HSPA6 has a role in genome replication by simply measuring the vRNA level. However, as a protein chaperone, HSPA6 may affect viral replication through helping proper folding of the viral proteins constituting replication complex. Thus, we investigated whether HSPA6 stabilized replication complex components 2C, 3Cpro, and 3Dpol by CHX chase assay. EV-A71-infected WT RD and HSPA6 KO RD cells were treated with translation inhibitor CHX at 9 hpi. The remaining 2C, 3Cpro, and 3Dpol were chased for another 1, 2, 4, and 6 h and measured by Western analysis (Figures 5A–C and Supplementary Figure 3); in addition, the mean intensity of three sets of experiments for bands specific for 2C, 3Cpro, and 3Dpol was plotted. There were no significant differences in protein stability between 2C (Figure 5A), 3Cpro (Figure 5B), and 3Dpol (Figure 5C) prepared from WT RD and HSPA6 KO RD cells. Consistently, a normalization of cell-associated vRNA levels (Figure 5D) with viral 3Dpol expression (Figure 5E) at 6 hpi, deduced as replication efficiency, showed no differences between WT RD and HSPA6 KO RD cells (Figure 5F). Collectively, these data suggest that HSPA6 does not regulate EV-A71 replication.
FIGURE 5
Knockout of HSPA6 Does Not Reduce Virion Assembly and Release Efficiency of EV-A71
We showed that EV-A71 production was lower in the absence of HSPA6 (Figure 2D) and higher in the presence of additional HSPA6 (Figure 2G). It is possible that other than its roles in IRES-mediated translation, HSPA6 is involved in viral assembly or release. To explore whether HSPA6 affects EV-A71 particles formation, WT RD and HSPA6 KO RD cells were challenged with EV-A71, and the total virions and total viral RNA prepared from cell-associated cells and extracellular viral particles were examined at 9 hpi. As expected, the total production of virions (Figure 6A) and vRNA (Figure 6B) were significantly reduced in HSPA6 KO RD cells since HSPA6 affects viral translation. To separate the effects of HSPA6 knockout on viral assembly from IRES-mediated translation, the ratio of total viral particle over total vRNA (virion/vRNA) was used to represent assembly efficiency. The result showed that the assembly efficiency of EV-A71 is similar in WT RD and HSPA6 KO RD cells (Figure 6C), suggesting that HSPA6 does not regulate EV-A71 virion assembly. Finally, we asked whether HSPA6 was involved in EV-A71 virion release. We considered the ratio of extracellular virion to total virion as release efficiency. The extracellular virion from culture supernatant and total virion at 12 hpi were harvested from WT RD and HSPA6 KO RD cells infected with EV-A71. There were no differences found in viral titers of extracellular virion (Figure 6D), total virion (Figure 6E), and release efficiency (Figure 6F) at 12 hpi between WT RD and HSPA6 KO RD cells. Put together, we concluded that HSPA6 played no role in either EV-A71 assembly and release.
FIGURE 6
Finally, we asked whether HSPA6 was involved in EV-A71 virion release. We considered the ratio of extracellular virion to total virion as release efficiency. The extracellular virion from culture supernatant and total virion were harvested at 12 hpi from WT RD and HSPA6 KO RD cells infected with EV-A71. There were no significant differences found in viral titers of extracellular virion (Figure 6D), total virion (Figure 6E), and release efficiency (Figure 6F) between WT RD and HSPA6 KO RD cells. Put together, we conclude that HSPA6 plays no role in either EV-A71 assembly or release.
HSPA6 Facilitates IRES Activities From Other Viruses
The IRES-Luc activity was reduced comparably in HSPA6-depleted cells in the presence (Figures 4E,F) or absence (Figures 4G,H) of EV-A71 infection, suggesting that HSPA6 facilitated the IRES activity of EV-A71 through chaperoning cellular proteins rather than viral proteins. We then asked if HSPA6 could influence the IRES activities of other viruses. To address this question, individual luciferase reporter driven by the IRES from CV-A16, echovirus 9, EMCV, or HCV was used. The in vitro transcribed reporter RNA was transfected into HSPA6-knockdown HeLa cells except the RNA of HCV IRES-Luc that was transfected into HSPA6-knockdown Huh7 cells. The luciferase activities were examined at 6 h post transfection and normalized with amounts of RNA transfected. Intriguingly, the results showed that the luciferase activity was reduced for all four IRES-Luc constructs in HSPA6-knockdown cells (Figures 7A–D), suggesting that HSPA6 may assist the function of cellular proteins commonly required for these viral IRES activities.
FIGURE 7
Discussion
Viral proteins are made in a large quantity in a short period of time during viral infection. To ensure proper folding of viral proteins, viruses often manipulate cellular chaperone proteins in favor of their own replication. The HSP70s, composed of a large chaperone protein family, play important roles in maintaining cellular homeostasis (). On the other hand, their participation in viral replication cycle is often a result of viral exploitation (; ; Wan et al., 2020). In our previous study, we found that HSPA1, HSPA8 and HSPA9, three major members of HSP70, play multiple functions in the EV-A71 life cycle (). Here we further reported that HSPA6, a scarcely studied HSP70 family member, was also involved in EV-A71 infection. Being a strictly stress-inducible HSP (, ), we found that HSPA6 protein production was induced by EV-A71 infection fittingly and reached a peak at the middle stage (6–9 hpi) of the infection cycle (Figure 1A). The knockout of HSPA6 led to the negative impacts on EV-A71 viral proteins, viral RNA and virions (Figures 2B–D), while the addition of HSPA6 had the positive effects (Figures 2E–G), indicating that HSPA6 was a positive regulator for the EV-A71 life cycle. Unlike other HSP70 isoforms we reported, which usually participate in multiple stages of the EV-A71 life (), HSPA6 was required for the IRES-mediated translation only (Figures 3–6). Surprisingly, HSPA6 regulated the IRES activity in the absence of viral proteins (Figures 4G,H), suggesting that HSPA6 facilitated EV-A71 IRES activity through cellular proteins instead of viral proteins.
An interesting question raised here is how HSPA6 is induced. Viruses could regulate host HSPs at different levels such as transcription, translation, post-translational modification and cellular localization (). Our preliminary data indicated that the HSPA6 mRNA levels were greatly induced after EV-A71 infection (data not shown), suggesting that EV-A71 upregulated HSPA6 at least at the transcription level. The transcription of stress-inducible HSP70s can be controlled by heat shock factors (HSFs). A sequence analysis of HSP6A (HSP70B’) genome has found potential heat-shock elements (HSEs) recognized by HSFs in the promoter region starting at nucleotide residue −72 (transcription initiation site: +1). Additional HSEs located between −647 and +48 were identified in a subsequent study Under unstressed conditions, HSF is maintained as an inert monomeric form through its interactions with chaperones such as HSP90 and HSP70. In response to physiological stresses, HSF is released from chaperone and binds to HSEs in the HSP gene promoters (, ). The nuclear localization activity of HSF can be further regulated by the phosphorylation mode carried out by calcium- or phospholipid-dependent protein kinase C (PKC) or by calcium/calmodulin-dependent protein kinase II (CaMKII) (). Since EV-A71 infection induces calcium influx (; ), we postulate that the calcium related protein kinases are activated upon viral infection to phosphorylate HSFs, leading to their nuclear entry. The binding of activated HSFs to the HSPA6 promoter may account for HSPA6 induction since multiple HSEs are present in its promoter region (; ) (This paragraph has been shortened as requested by editor).
IRES-mediated translation is used by many viruses to avoid the shut off of cap-dependent translation caused by viral infection. Different types of IRES use distinct ITAFs for their individual IRES activities, but may share some common host factors (; ). For example, La protein (also known as Sjogren syndrome antigen B) has been found to regulate type I IRES activities from CV-B3 (), poliovirus (), and hepatitis A virus (); it also regulates type II IRES from EMCV () and type III IRES from HCV (). In this study, we found that HSPA6 was a positive regulator for EV-A71 IRES (type I)-mediated translation independent of viral proteins (Figure 4), suggesting that HSPA6 acts on cellular factors rather than viral proteins to modulate EV-A71 translation. Moreover, we found that two other type I IRESs from CV-A16 and echovirus 9 (Figures 7A,B), type II IRES from EMCV (Figure 7C), and type III IRES from HCV (Figure 7D) were also regulated by HSPA6, further suggesting that HSPA6 may act on a common ITAF or ITAFs. It has been reported that HSPA1 induces La protein production which in turn enhances the IRES-mediated translation of CV-B3 (Wang et al., 2017). Whether HSPA6 affects La protein production/function is unclear. Other examples of ITAFs including PTBP1, PCBP2 and hnRNP D (also known as AUF1) are known to regulate various types of viral IRESs as well [reviewed by ] these ITAFs could therefore be the targets of HSPA6. Alternatively, yet-to-be-identified ITAFs regulated by HSPA6 could be responsible for the enhancement of the IRES activities. Another interesting question is how HSPA6 activates the IRES activity. It has been proposed that HSP70 chaperones enhance IRES activity by various mechanisms. To name a few possibilities, HSPA6 may facilitate the production, the folding and the transport of ITAFs, as well as the final assembly of translation-competent ribonucleoprotein complex. Alternatively, HSPA6 might enhance viral IRESs by its potential RNA binding activity since its association with HCV 3-NT′R was reported ().
Both HSPA1 and HSPA6 are stress-induced HSP70s with high protein sequence homology (; ). While HSPA6 may share overlapping functions with HSPA1, we showed that they have non-redundant function during EV-A71 infection. This is demonstrated by the knockout of HSPA6 still reduced EV-A71 replication via reducing the IRES activity (Figures 2, 4). Consistently, our prior studies also showed that knockdown of HSPA1, in the presence of HSPA6, impaired several stages of EV-A71 life cycle (). In summary, we demonstrated not only that HSPA6 was induced during EV-A71 infection to facilitate its IRES-mediated translation, but also that it played roles in the IRESs from other viruses. There are limited studies about HSPA6, among them only one report showing its association with the 3′UTR of the HCV genome (). We provide the very first report functionally, which demonstrates HSPA6, a novel inducible HSP70 member, impacts a viral life cycle.
Statements
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 author/s.
Author contributions
Y-SS, L-HH, and C-JC conceived the project and wrote the manuscript. Y-SS conducted the experiments. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the Ministry of Science and Technology, Taiwan (MOST 108-2320-B-010-028) to L-HH, and Ministry of Science and Technology, Taiwan (MOST 107-2320-B-010-005), Yen Tjing Ling Medical Foundation (CI-108-31 and CI-110-26), and Far East Memorial Hospital (109DN22 and 110DN24) to C-JC.
Acknowledgments
We thank Shin-Ru Shih of the Chang-Gung University, Taiwan, Szu-Hao Kung of the National Yang-Ming University, Taiwan, and Hiroyuki Shimizu of the National Institute of Infectious Diseases, Musashimurayama, Japan for generously providing materials.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2021.664955/full#supplementary-material
References
1
BaggenJ.ThibautH. J.StratingJ. R. P. M.Van KuppeveldF. J. M. (2018). The life cycle of non-polio enteroviruses and how to target it.Nat. Rev. Microbiol.16368–381. 10.1038/s41579-018-0005-4
2
BasavappaR.SyedR.FloreO.IcenogleJ. P.FilmanD. J.HogleJ. M. (1994). Role and mechanism of the maturation cleavage of VP0 in poliovirus assembly: structure of the empty capsid assembly intermediate at 2.9 A resolution.Protein Sci.31651–1669. 10.1002/pro.5560031005
3
BirdS. W.MaynardN. D.CovertM. W.KirkegaardK. (2014). Nonlytic viral spread enhanced by autophagy components.Proc. Natl. Acad Sci. U.S.A.11113081–13086. 10.1073/pnas.1401437111
4
BolhassaniA.AgiE. (2019). Heat shock proteins in infection.Clin. Chim. Acta49890–100.
5
ChenY. H.DuW.HagemeijerM. C.TakvorianP. M.PauC.CaliA.et al (2015). Phosphatidylserine vesicles enable efficient en bloc transmission of enteroviruses.Cell160619–630. 10.1016/j.cell.2015.01.032
6
ChenY.-J.ChenY.-H.ChowL.-P.TsaiY.-H.ChenP.-H.HuangC.-Y. F.et al (2010). Heat shock protein 72 is associated with the hepatitis C virus replicase complex and enhances viral RNA replication.J. Biol. Chem.28528183–28190. 10.1074/jbc.m110.118323
7
ChoiK.KimJ. H.LiX.PaekK. Y.HaS. H.RyuS. H.et al (2004). Identification of cellular proteins enhancing activities of internal ribosomal entry sites by competition with oligodeoxynucleotides.Nucleic Acids Res.321308–1317. 10.1093/nar/gkh300
8
ChuangC.-K.YangT.-H.ChenT.-H.YangC.-F.ChenW.-J. (2015). Heat shock cognate protein 70 isoform D is required for clathrin-dependent endocytosis of Japanese encephalitis virus in C6/36 cells.J. Gen. Virol.96793–803. 10.1099/jgv.0.000015
9
CongH.DuN.YangY.SongL.ZhangW.TienP. (2016). Enterovirus 71 2B Induces cell apoptosis by directly inducing the conformational activation of the proapoptotic protein Bax.J. Virol.90:9862. 10.1128/jvi.01499-16
10
cordesS.KusovY.HeiseT.Gauss-MullerV. (2008). La autoantigen suppresses IRES-dependent translation of the hepatitis A virus.Biochem. Biophys. Res. Commun.3681014–1019. 10.1016/j.bbrc.2008.01.163
11
Costa-MattioliM.SvitkinY.SonenbergN. (2004). La autoantigen is necessary for optimal function of the poliovirus and hepatitis C virus internal ribosome entry site in vivo and in vitro.Mol. Cell Biol.246861–6870. 10.1128/mcb.24.15.6861-6870.2004
12
DanX.WanQ.YiL.LuJ.JiaoY.LiH.et al (2019). Hsp27 responds to and facilitates enterovirus A71 replication by enhancing viral internal ribosome entry site-mediated translation.J. Virol.93:e02322–18.
13
DaugaardM.RohdeM.JäätteläM. (2007). The heat shock protein 70 family: highly homologous proteins with overlapping and distinct functions.FEBS Lett.5813702–3710. 10.1016/j.febslet.2007.05.039
14
de BreyneS.BonderoffJ. M.ChumakovK. M.LloydR. E.HellenC. U. T. (2008). Cleavage of eukaryotic initiation factor eIF5B by enterovirus 3C proteases.Virology378118–122.10.1016/j.virol.2008.05.019
15
DongQ.MenR.DanX.ChenY.LiH.ChenG.et al (2018). Hsc70 regulates the IRES activity and serves as an antiviral target of enterovirus A71 infection.Antivir. Res.15039–46. 10.1016/j.antiviral.2017.11.020
16
FengZ.HensleyL.McknightK. L.HuF.MaddenV.PingL.et al (2013). A pathogenic picornavirus acquires an envelope by hijacking cellular membranes.Nature496367–371. 10.1038/nature12029
17
GradiA.SvitkinY. V.ImatakaH.SonenbergN. (1998). Proteolysis of human eukaryotic translation initiation factor eIF4GII, but not eIF4GI, coincides with the shutoff of host protein synthesis after poliovirus infection.Proc. Natl. Acad. Sci. U.S.A.9511089–11094. 10.1073/pnas.95.19.11089
18
HaghighatA.SvitkinY.NovoaI.KuechlerE.SkernT.SonenbergN. (1996). The eIF4G-eIF4E complex is the target for direct cleavage by the rhinovirus 2A proteinase.J. Virol.708444–8450. 10.1128/jvi.70.12.8444-8450.1996
19
HansonP. J.ZhangH. M.HemidaM. G.YeX.QiuY.YangD. (2012). IRES-dependent translational control during virus-induced endoplasmic reticulum stress and apoptosis.Front. Microbiol.3:92. 10.3389/fmicb.2012.00092
20
HarrisD.ZhangZ.ChaubeyB.PandeyV. N. (2006). Identification of cellular factors associated with the 3′-nontranslated region of the hepatitis C virus genome.Mol. Cell. Proteomics5:1006. 10.1074/mcp.m500429-mcp200
21
HouH.-Y.LuW.-W.WuK.-Y.LinC.-W.KungS.-H. (2016). Idarubicin is a broad-spectrum enterovirus replication inhibitor that selectively targets the virus internal ribosomal entry site.J. Gen. Virol.971122–1133. 10.1099/jgv.0.000431
22
HungC. T.KungY. A.LiM. L.BrewerG.LeeK. M.LiuS. T.et al (2016). Additive promotion of viral internal ribosome entry site-mediated translation by far upstream element-binding protein 1 and an enterovirus 71-induced cleavage product.PLoS Pathog.12:e1005959. 10.1371/journal.ppat.1005959
23
HussainK. M.LeongK. L. J.NgM. M.-L.ChuJ. J. H. (2011). The essential role of clathrin-mediated endocytosis in the infectious entry of human enterovirus 71.J. Biol. Chem.286309–321. 10.1074/jbc.m110.168468
24
IlnytskaO.SantianaM.HsuN. Y.DuW. L.ChenY. H.ViktorovaE. G.et al (2013). Enteroviruses harness the cellular endocytic machinery to remodel the host cell cholesterol landscape for effective viral replication.Cell Host Microbe14281–293. 10.1016/j.chom.2013.08.002
25
JiangH.WengL.ZhangN.AritaM.LiR.ChenL.et al (2011). Biochemical characterization of enterovirus 71 3D RNA polymerase.Biochim. Biophys. Acta (BBA) Gene Regul. Mechan.1809211–219. 10.1016/j.bbagrm.2011.01.001
26
KimY. K.JangS. K. (1999). La protein is required for efficient translation driven by encephalomyocarditis virus internal ribosomal entry site.J. Gen. Virol.80 (Pt 12)3159–3166. 10.1099/0022-1317-80-12-3159
27
KräusslichH. G.NicklinM. J.ToyodaH.EtchisonD.WimmerE. (1987). Poliovirus proteinase 2A induces cleavage of eucaryotic initiation factor 4F polypeptide p220.J. Virol.612711–2718. 10.1128/jvi.61.9.2711-2718.1987
28
Kuyumcu-MartinezN. M.JoachimsM.LloydR. E. (2002). Efficient cleavage of ribosome-associated poly(A)-binding protein by enterovirus 3C protease.J. Virol.762062–2074. 10.1128/jvi.76.5.2062-2074.2002
29
Kuyumcu-MartinezN. M.Van EdenM. E.YounanP.LloydR. E. (2004). Cleavage of poly(A)-binding protein by poliovirus 3C protease inhibits host cell translation: a novel mechanism for host translation shutoff.Mol. Cell Biol.241779–1790. 10.1128/mcb.24.4.1779-1790.2004
30
LamphearB. J.YanR.YangF.WatersD.LiebigH. D.KlumpH.et al (1993). Mapping the cleavage site in protein synthesis initiation factor eIF-4 gamma of the 2A proteases from human Coxsackievirus and rhinovirus.J. Biol. Chem.26819200–19203. 10.1016/s0021-9258(19)36499-3
31
LeeK. M.ChenC. J.ShihS. R. (2017). Regulation mechanisms of viral IRES-Driven translation.Trends Microbiol.25546–561. 10.1016/j.tim.2017.01.010
32
LeungT. K.RajendranM. Y.MonfriesC.HallC.LimL. (1990). The human heat-shock protein family. Expression of a novel heat-inducible HSP70 (HSP70B’) and isolation of its cDNA and genomic DNA.Biochem. J.267125–132. 10.1042/bj2670125
33
LevengoodJ. D.TolbertM.LiM. L.TolbertB. S. (2013). High-affinity interaction of hnRNP A1 with conserved RNA structural elements is required for translation and replication of enterovirus 71.RNA Biol.101136–1145. 10.4161/rna.25107
34
LiJ.YaoY.ChenY.XuX.LinY.YangZ.et al (2017). Enterovirus 71 3C promotes apoptosis through cleavage of PinX1, a telomere binding protein.Journal of virology91:e02016–16.
35
LinH.-Y.YangY.-T.YuS.-L.HsiaoK.-N.LiuC.-C.SiaC.et al (2013). Caveolar endocytosis is required for human PSGL-1-mediated enterovirus 71 infection.J. Virol.87:9064. 10.1128/jvi.00573-13
36
LinJ.-Y.BrewerG.LiM.-L. (2015). HuR and Ago2 bind the internal ribosome entry site of enterovirus 71 and promote virus translation and replication.PLoS One10:e0140291. 10.1371/journal.pone.0140291
37
LinJ.-Y.ShihS.-R.PanM.LiC.LueC.-F.StollarV.et al (2009). hnRNP a1 interacts with the 5′ untranslated regions of enterovirus 71 and sindbis virus RNA and is required for viral replication.J. Virol.83:6106. 10.1128/jvi.02476-08
38
LozanoG.Martínez-SalasE. (2015). Structural insights into viral IRES-dependent translation mechanisms.Curr. Opin. Virol.12113–120. 10.1016/j.coviro.2015.04.008
39
LuJ. R.LuW. W.LaiJ. Z.TsaiF. L.WuS. H.LinC. W.et al (2013). Calcium flux and calpain-mediated activation of the apoptosis-inducing factor contribute to enterovirus 71-induced apoptosis.J. Gen. Virol.941477–1485. 10.1099/vir.0.047753-0
40
LuoZ.DongX.LiY.ZhangQ.KimC.SongY.et al (2014). PolyC-binding protein 1 interacts with 5′-untranslated region of enterovirus 71 RNA in membrane-associated complex to facilitate viral replication.PLoS One9:e87491. 10.1371/journal.pone.0087491
41
MayerM. P. (2013). Hsp70 chaperone dynamics and molecular mechanism.Trends Biochem. Sci.38507–514. 10.1016/j.tibs.2013.08.001
42
McMinnP. C. (2002). An overview of the evolution of enterovirus 71 and its clinical and public health significance.FEMS Microbiol. Rev.2691–107. 10.1111/j.1574-6976.2002.tb00601.x
43
MeerovitchK.PelletierJ.SonenbergN. (1989). A cellular protein that binds to the 5′-noncoding region of poliovirus RNA: implications for internal translation initiation.Genes Dev.31026–1034. 10.1101/gad.3.7.1026
44
MorimotoR. I. (1993). Cells in stress: transcriptional activation of heat shock genes.Science2591409–1410. 10.1126/science.8451637
45
MorimotoR. I. (1998). Regulation of the heat shock transcriptional response: cross talk between a family of heat shock factors, molecular chaperones, and negative regulators.Genes Dev.123788–3796. 10.1101/gad.12.24.3788
46
MorimotoR. I.KlineM. P.BimstonD. N.CottoJ. J. (1997). The heat-shock response: regulation and function of heat-shock proteins and molecular chaperones.Essays Biochem.3217–29.
47
NainM.MukherjeeS.KarmakarS. P.PatonA. W.PatonJ. C.AbdinM. Z.et al (2017). GRP78 Is an important host factor for japanese encephalitis virus entry and replication in mammalian cells.J. Virol.91:e2274–16.
48
NoonanE. J.PlaceR. F.GiardinaC.HightowerL. E. (2007a). Hsp70B’ regulation and function.Cell Stress Chaperones12393–402. 10.1379/csc-278e.1
49
NoonanE. J.PlaceR. F.RasoulpourR. J.GiardinaC.HightowerL. E. (2007b). Cell number-dependent regulation of Hsp70B’ expression: evidence of an extracellular regulator.J. Cell Physiol.210201–211. 10.1002/jcp.20875
50
PaulA. V.WimmerE. (2015). Initiation of protein-primed picornavirus RNA synthesis.Virus Res.20612–26. 10.1016/j.virusres.2014.12.028
51
RamirezV. P.StamatisM.ShmuklerA.AneskievichB. J. (2015). Basal and stress-inducible expression of HSPA6 in human keratinocytes is regulated by negative and positive promoter regions.Cell Stress Chaperones2095–107. 10.1007/s12192-014-0529-0
52
RayP. S.DasS. (2002). La autoantigen is required for the internal ribosome entry site-mediated translation of Coxsackievirus B3 RNA.Nucleic Acids Res.304500–4508. 10.1093/nar/gkf583
53
RobinsonS. M.TsuengG.SinJ.MangaleV.RahawiS.McintyreL. L.et al (2014). Coxsackievirus B exits the host cell in shed microvesicles displaying autophagosomal markers.PLoS Pathog.10:e1004045. 10.1371/journal.ppat.1004045
54
SaibilH. (2013). Chaperone machines for protein folding, unfolding and disaggregation.Nat. Rev. Mol. Cell Biol.14630–642. 10.1038/nrm3658
55
SantoroM. G.AmiciC.RossiA. (2009). “Role of heat shock proteins in viral infection,” in Prokaryotic and Eukaryotic Heat Shock Proteins in Infectious Disease, Vol. 4edsPockleyA. G.SantoroM. G.CalderwoodS. K. (New York, NY: Springer) 51–84.
56
SantoroM. G.AmiciC.RossiA. (2010). “Role of heat shock proteins in viral infection,” in Prokaryotic and Eukaryotic Heat Shock Proteins in Infectious Disease, edsPockleyA. G.CalderwoodS. K.SantoroM. G. (Dordrecht: Springer Netherlands) 51–84. 10.1007/978-90-481-2976-8_3
57
SilverJ. T.NobleE. G. (2012). Regulation of survival gene hsp70.Cell Stress Chaperones171–9. 10.1007/s12192-011-0290-6
58
SommergruberW.AhornH.KlumpH.SeipeltJ.ZoephelA.FesslF.et al (1994). 2A proteinases of coxsackie- and rhinovirus cleave peptides derived from eIF-4 gamma via a common recognition motif.Virology198741–745. 10.1006/viro.1994.1089
59
StricherF.MacriC.RuffM.MullerS. (2013). HSPA8/HSC70 chaperone protein: structure, function, and chemical targeting.Autophagy91937–1954. 10.4161/auto.26448
60
SuY. S.HsiehP. Y.LiJ. S.PaoY. H.ChenC. J.HwangL. H. (2020). The Heat shock protein 70 family of chaperones regulates all phases of the enterovirus A71 life cycle.Front. Microbiol.11:1656. 10.3389/fmicb.2020.01656
61
SuY.-S.TsaiA.-H.HoY.-F.HuangS.-Y.LiuY.-C.HwangL.-H. (2018). Stimulation of the internal ribosome entry site (IRES)-dependent translation of enterovirus 71 by DDX3X RNA helicase and viral 2A and 3C proteases.Front. Microbiol.9:1324. 10.3389/fmicb.2018.01324
62
SupasornO.TongtaweP.SrimanoteP.RattanakomolP.ThanongsaksrikulJ. (2020). A nonstructural 2B protein of enterovirus A71 increases cytosolic Ca(2+) and induces apoptosis in human neuroblastoma SH-SY5Y cells.J. Neurovirol.26201–213. 10.1007/s13365-019-00824-0
63
SweeneyT. R.AbaevaI. S.PestovaT. V.HellenC. U. (2014). The mechanism of translation initiation on Type 1 picornavirus IRESs.EMBO J.3376–92. 10.1002/embj.201386124
64
TaguwaS.MaringerK.LiX.Bernal-RubioD.Rauch JenniferN.Gestwicki JasonE.et al (2015). Defining Hsp70 subnetworks in dengue virus replication reveals key vulnerability in flavivirus infection.Cell1631108–1123. 10.1016/j.cell.2015.10.046
65
ThompsonS. R.SarnowP. (2003). Enterovirus 71 contains a type I IRES element that functions when eukaryotic initiation factor eIF4G is cleaved.Virology315259–266. 10.1016/s0042-6822(03)00544-0
66
TooI. H. K.YeoH.SessionsO. M.YanB.LibauE. A.HoweJ. L. C.et al (2016). Enterovirus 71 infection of motor neuron-like NSC-34 cells undergoes a non-lytic exit pathway.Sci. Rep.6:36983.
67
TriantafilouK.FradeliziD.WilsonK.TriantafilouM. (2002). GRP78, a coreceptor for coxsackievirus A9, interacts with major histocompatibility complex class I molecules which mediate virus internalization.J. Virol.76:633. 10.1128/jvi.76.2.633-643.2002
68
van der SchaarH. M.MeliaC. E.Van BruggenJ. A. C.StratingJ. R. P. M.Van GeenenM. E. D.KosterA. J.et al (2016). Illuminating the sites of enterovirus replication in living cells by using a split-GFP-tagged viral protein.mSphere1e00104–e00116.
69
WanQ.SongD.LiH.HeM.-L. (2020). Stress proteins: the biological functions in virus infection, present and challenges for target-based antiviral drug development.Signal Transduct. Target. Ther.5125.
70
WangF.QiuY.ZhangH. M.HansonP.YeX.ZhaoG.et al (2017). Heat shock protein 70 promotes coxsackievirus B3 translation initiation and elongation via Akt-mTORC1 pathway depending on activation of p70S6K and Cdc2.Cell Microbiol.19:e12725. 10.1111/cmi.12725
71
XiJ.YeF.WangG.HanW.WeiZ.YinB.et al (2019). Polypyrimidine tract-binding protein regulates enterovirus 71 translation through interaction with the internal ribosomal entry site.Virol. Sin.3466–77. 10.1007/s12250-019-00089-1
72
YiE.-J.ShinY.-J.KimJ.-H.KimT.-G.ChangS.-Y. (2017). Enterovirus 71 infection and vaccines.Clin. Exp. Vaccine Res.64–14. 10.7774/cevr.2017.6.1.4
73
ZárateS.CuadrasM. A.EspinosaR.RomeroP.JuárezK. O.Camacho-NuezM.et al (2003). Interaction of rotaviruses with Hsc70 during cell entry is mediated by VP5.J. Virol.77:7254. 10.1128/jvi.77.13.7254-7260.2003
74
ZhangH.SongL.CongH.TienP. (2015). Nuclear protein Sam68 interacts with the enterovirus 71 internal ribosome entry site and positively regulates viral protein translation.J. Virol.8910031–10043. 10.1128/jvi.01677-15
Summary
Keywords
enterovirus A71 (EV-A71), HSPA6, internal ribosomal entry site, viral IRES, induced HSP70
Citation
Su Y-S, Hwang L-H and Chen C-J (2021) Heat Shock Protein A6, a Novel HSP70, Is Induced During Enterovirus A71 Infection to Facilitate Internal Ribosomal Entry Site-Mediated Translation. Front. Microbiol. 12:664955. doi: 10.3389/fmicb.2021.664955
Received
06 February 2021
Accepted
12 April 2021
Published
07 May 2021
Volume
12 - 2021
Edited by
Shiu-Wan Chan, The University of Manchester, United Kingdom
Reviewed by
Ming-Liang He, City University of Hong Kong, Hong Kong; Marcelo Lopez-Lastra, Pontificia Universidad Católica de Chile, Chile
Updates
Copyright
© 2021 Su, Hwang and Chen.
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*Correspondence: Lih-Hwa Hwang, lhhwang@ym.edu.twChi-Ju Chen, cjchen@ym.edu.tw
This article was submitted to Virology, a section of the journal Frontiers in Microbiology
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