MicroRNAs (miRNAs) regulate virus replication through multiple mechanisms. Poliovirus causes a highly debilitating disease and though global efforts to eradicate polio have sharply decreased polio incidence, unfortunately three countries (Afghanistan, Nigeria and Pakistan) remain polio-endemic. We hypothesize that understanding the host factors involved in polio replication will identify novel prophylactic and therapeutic targets against polio and related viruses. In this data set, employing genome wide screens of miRNA mimics and inhibitors, we identified miRNAs which significantly suppressed polio replication. Specifically, miR-134 regulates poliovirus replication via modulation of ras-related nuclear protein (RAN), an important component of the nuclear transport system. MiR-134 also inhibited other Picornaviridae viruses including EV71, a growing concern and a high priority for vaccination in Asian countries like China. These findings demonstrate a novel mechanism for miRNA regulation of poliovirus and other Picornaviridae viruses in host cells, and thereby may provide a novel approach in combating infection and a potential approach for the development of anti-Picornaviridae strategies.
Background and Summary
Poliovirus (PV), a non-enveloped human enterovirus virus of the Picornaviridae family is the etiological agent of poliomyelitis (polio). Poliovirus symptoms include fever, fatigue, headache, limb pain and permanent paralysis in some cases. Global vaccination campaigns utilizing live-attenuated oral polio vaccines have reduced PV in all but three countries (Afghanistan, Nigeria and Pakistan) which still remain PV-endemic. The global use of live-attenuated vaccines has an increased risk of reversion to wild type and shedding by immune-deficient individuals1,2. Though vaccination is effective, treatment of polio is symptomatic. Enterovirus 71 (EV71), a relative of PV, is a major public health burden in the Western Pacific region associated with severe neurologic symptoms of hand, foot and mouth disease (HFMD), a disease most often contracted by children<5 years old3. More than 7 million cases of HFMD were reported in mainland China from 2008–2012. EV71 vaccination programs are challenged by high cost and vaccine availability4. Understanding host gene networks that regulate PV and/or EV71 replication, and development of agents against these targets is a promising strategy to prevent and treat PV while eliminating the issues of reversion and shedding.
RNA interference (RNAi) is an evolutionarily conserved pathway of post transcriptional gene regulation involving small double-stranded non-coding RNAs, microRNAs (miRNAs). The ‘guide’ strand contains a 6 nt ‘seed’ region that binds complementary miRNA recognition elements (MRE) within the 3′ untranslated regions (3′-UTR) of transcripts in a RNA induced silencing complex (RISC) causing degradation of transcripts or blocking gene translation5,6. PV and EV71 can modulate multiple host pathways including RNAi for their own replication7,
HEp-2C cells were reverse-transfected with non-targeting siRNA, miRNA negative controls, or gene specific mimics for 48 h. The gene specific mimics corresponded to 1,208 known miRNAs in the human genome. Cytotoxicity was evaluated via CytoTox-Glo assay (Promega). Mimics which were not cytotoxic were evaluated. Transfected cells were either mock infected (no virus) or infected with Sabin-2 strains of PV (MOI 0.01) or EV71 (MOI 0.01). EV71 was examined in miRNA-transfected cells, but was not used as part of the entire library screen.
We investigated whether miRNA-transfection with miR-134 inhibited EV71 replication. Mimics/inhibitors against the C. elegans miR-67 were used as non-targeting controls while siRNAs targeting the PV capsid (siPol) were used as positive control. Twenty-four hours post-infection, cells were stored at −80 °C. miRNA effects on Sabin-2 replication were evaluated by a PV type-II specific ELISA14,15. Absorbance values were normalized to non-targeting miRNA mimic controls and converted to a z-score. Mimics that resulted in a z-score≤−1.5 s.d. were deemed hits and subjected to validation experiments which utilized miRNA inhibitors targeting the same genes (Table 1). Several miRNAs suppressed PV replication. MiR-134 and miR-138 had the most potent antiviral effect against PV Sabin-2 following transfection (Fig. 1). For this reason, the antiviral effects of miR-134 were evaluated further and the resulting data is outlined here. MiR-138 is currently still under evaluation. Ingenuity pathway analysis (IPA; QIAGEN) was utilized to evaluate protein networks associated with PV replication to predict targets of miR-134 that may be involved in PV replication. TargetScan analysis was used to predict target transcripts via seed region complementarity. IPA and TargetScan analysis revealed many predicted targets, of interest was the nuclear transport system protein (RAN) because it miR-197 inhibited EV72 replication16. We confirmed by qPCR of RAN mRNA and miR-134 transcript levels following miR-mimic transfection (Fig. 2). To confirm RAN’s role in PV replication, RAN was silenced via siRNA i prior to infection with Sabin-2 PV. Silencing inhibited PV replication in both cell lines (Fig. 3). miR-134 also drastically reduced EV71 replication (Fig. 4). It is also possible that miR-134 may regulate other host genes required for PV replication, which is supported by the evidence that one miRNA can regulate large numbers of target mRNAs17. Hits from primary screen were validated using miRNA specific inhibitors. These findings demonstrate miRNA regulation of PV and EV71 and may provide a novel approach in combating infection.
Cell culture and viruses
HEp-2 is an adherent human epidermoid carcinoma cell line that support PV replication. Caco-2 cells, a colorectal adenocarcinoma (HTB-37) adherent epithelial cell line derived from human colon tissue, were used in conjunction with HEp-2 cells to evaluate the antiviral effects of miR-134 against PV replication. Effects of target gene silencing on poliovirus replication can be detected 24–48 h post-infection (pi), and were utilized for the miRNA screen. Human muscle rhabdomyosarcoma (RD) cells are an adherent cell which supports enterovirus 71 (EV 71) replication and are routinely utilized to determine enterovirus titers post-miRNA transfection. All cell lines were cultured under the same conditions. All experiments were completed with cells at the same passage. As part of this study we investigated whether miRNA-transfection with miR-134 also inhibited replication of EV71, a familial relative of PV, in an effort to evaluate whether viruses within the same family exhibiting similar replication pathways would also be affected by miR-134. These experiments utilized the same negative control miRNA and siRNA as the PV evaluation18.
Briefly, cells were cultured in Dulbecco’s modified eagle medium (DMEM; Hyclone) supplemented with 10% heat-inactivated fetal bovine serum (FBS) under cell culture conditions (37 °C, 5% CO2). Cells were passaged 24 h prior to transfection. Briefly, cell culture media was removed and cells washed with 1X PBS to remove excess media and FBS. Following washing, cells were detached from the culture flask via addition and incubation with 0.05% Trypsin. Cells were incubated with trypsin under cell culture conditions until cells detached from the flask surface. Trypsin was neutralized with equal volumes of cell culture media containing 10% FBS. Trypsonized cells were removed from the cell culture flask and transferred to a 50 ml conical tube. Cell suspension was pelleted via centrifugation (1 min at 1,200×g). Supernatant was discarded and cells were resuspended in cell culture media containing 10% FBS by pipetting. Resuspended cells were then transferred back to the cell culture flask at the appropriate concentration and incubated under cell culture conditions. Master cell stocks were cultivated and stored at −80 °C. Passage numbers were kept consistent throughout all experiments to reduce variability. HEp-2Cand Caco-2 cells were utilized at P164 and P46, respectively.
The Sabin-2 PV vaccine strain was used throughout this study. This strain of PV is propagated in the African Green Monkey Kidney cell line Vero-P, the approved cell line for polio vaccine production. Cell stocks were obtained from the Centers of Disease Control and Prevention (CDC, Atlanta) who in turn obtained stocks from the Serum Institute of India (SI). Vero-P stocks were cultured under cell culture conditions at 37 °C, 5% CO2 in Dulbecco’s modified Eagle’s medium (DMEM; Hyclone, GE Healthcare) supplemented with 10% heat inactivated fetal bovine serum (FBS; Hyclone, GE Healthcare). Master cell stocks were cultivated and stored at −80 °C. Passage number were kept consistent throughout all experiments to reduce variability. Viral stocks were cultivated, viral titers determined by plaque assay and 50% cell culture infectious dose (CCID50), aliquoted and stored at −80 °C until use19.
Primary screening and miRNA mimic transfection
The primary miRNA mimic screen included a library of 1,208 miRNA mimics (GE Dharmacon-Thermo Scientific; CS-001010 Human Mimics Lot 10100 and CS-001015 Supplement Human Mimic 16.0 Lot 11144). Screening was completed in triplicate using a 96-well plate format with HEp-2C cells (103 cells per well). HEp-2C cells were reverse transfected to a final mimic concentration of 25 nM. The Dharmacon miRIDIAN microRNA mimic negative control (miR-NTC; CN-001000-01) was used as a negative control and a siRNA targeting the poliovirus capsid-coding region (siPol) (CDC, provided by Dr Steve Oberste) was utilized to monitor silencing effects on poliovirus replication in all assays. A cytoxicity transfection control siRNA (siTOX) (GE Healthcare Dharmacon TOX Transfection Control, Cat. # D0015000120) was utilized to visually confirm effective productive transfection. Cells successfully transfected with siTOX undergo apoptosis resulting in cell death. Briefly, mimics were incubated at room temperature for 20 min in 0.3% (0.3 ul per well) of DharmaFECT transfection reagent 4 (DF4) (Dharmacon-Thermo Scientific) prepared in serum-free medium (Opti-MEM, Invitrogen Inc.) prior to addition of cells in Dulbecco’s modified Eagle’s medium (DMEM, Invitrogen) supplemented with 10% calf serum. Cells were cultured for 48 h at 37 °C, 5% CO2. Forty-eight hours post-transfection, media was removed, cells were washed with phosphate buffer saline (PBS; Hyclone, GE Healthcare) and infected with Sabin 2 at an MOI=0.01 Virus was diluted in DMEM containing 2% calf serum and 1% penicillin-streptomycin. Twenty-four hours post-infection, HEp-2C cells were removed from the culture incubator and stored at −80 °C until evaluated.
Validation screening and removal of false positives
Following the primary miRNA screen, in an effort to reduce false positives relative to transfection variability, individual miRNA inhibitors (GE Dharmacon Thermo-Fisher; IH-001010 Human Inhibitor Lot 09168 and IH-001015 Supplement Human Hairpin Inhibitor Library 16.0) were utilized to validate miRNA hits produced as part of the primary miRNA mimic screen. Hits producing an opposite phenotype as compared to the miRNA mimics screen were taken into future studies. The miRNA mimics are the focus of this study; therefore, the brief screening of the miRNA inhibitors was not included here and only used as a form of phenotype validation. Briefly, individual miRNA inhibitors corresponding to miRNA hits produced as part of the primary mimic screen were reverse-transfected into HEp-2 cells as previously described. At 48 h post-transfection, cells were infected with Sabin-1, Sabin-2 or Sabin-3 strains (MOI=0.01). Cells were incubated and replication assessed as previously stated. Messenger RNA levels for each gene were evaluated following transfection by qPCR.
Validation screens were completed to further confirm the anti-virus effects of the identified miRNA mimics using ELISA assay. For the list of 108 anti-polio miRNA mimics identified from the primary miRNA mimics screening (Table 1), we compared the phenotypes with the miRNA inhibitor data. Following miRNA inhibitor experiments, hits that did not result in opposing phenotypes when compared to their mimic counterparts were excluded. The miRNA mimics which lead to cell death were also excluded. We also identified 29 miRNA mimics that when transfected into cells lead to decreased poliovirus replication (Fig. 5). From this data, miRNA-134 was selected for further investigation in this study.
Polio Type II specific antibody-capture ELISA
A PV type-II specific ELISA was used to determine miRNA effects on Sabin-2 replication. Antibody-capture ELISA for detection of poliovirus was described previously14,15. Briefly, 2HB high-binding 96-well plates (NUNC; 1424561-PK) were coated with 50 ul of the PV type II specific monoclonal antibody (HYB294-06, mouse; Thermo Scientific Pierce) diluted in carbonate-bicarbonate buffer (pH 9.6). Plates were incubated for 16 h (overnight) at 4 °C in a moist chamber. Antibody-coated plates were washed with 0.05% phosphate buffered saline with Tween 20 (PBST). Following washing, plates were blocked with 100 μl blocking buffer (1x PBS containing 0.5% Gelatin and 0.25% Tween) for 60 min at 37 °C. Block was removed and plates were washed 4x with PBST. Fifty microliters of cell lysate was transferred from the thawed infected transfection plate to the antibody-coated plates. Inoculated plates were incubated for 60 min at 37 °C in a moist chamber. Subsequently, plates were washed 4x with PBST and 50 ul of HRP-substrate solution (SureBlue TMB) was added and incubated for 15 min at 37 °C. The reaction was halted by the addition of 50 ul H2SO4 stop solution. Absorbance was evaluated at a wavelength of 450 nm with a plate spectrophotometer (Tecan). Absorbance values were normalized to non-targeting miRNA mimic controls and converted to a z-score. Z-scores were used to determine whether hits are positive according to methods describe previously20. Hits with a z-score≤−1.5 s.d. were subjected to validation experiments in HEp-2C cells.
Poliovirus (PV) and enterovirus 71 (EV71) plaque assays
PV and EV71 viral titers were determined post-transfection by either a HEp-2 or RD cell-based plaque assay, respectively19,21. Briefly, 1.2×106 cells were seeded in each well of six well plates and incubated overnight under standard cell culture conditions. The next day culture media was removed and cells were washed with minimal essential medium (MEM; Hyclone, GE Healthcare, USA) supplemented with 2% fetal bovine serum (FBS). Next, samples were serially diluted 10-fold in MEM with 2% FBS and added to washed plates. Plates were incubated at 37 °C, 5% CO2 for 1 h. The inoculum was removed and plates were overlaid with 0.9% nutrient agarose gel in MEM supplemented with 2% FBS, followed by incubation in a 37 °C incubator with 5% CO2 for 3 days. Agarose overlay was removed and cells fixed with 10% formaldehyde in PBS. Plaques were visualized by staining with crystal violet. Virus titers were expressed as PFU ml−1.
RNA isolation and qRT-PCR
Cells were homogenized and total RNA was extracted using RNAzol RT reagent (Molecular Research Center) according to the manufacturer’s instruction. The concentration of the purified RNA was determined by NanoDrop spectrophotometer (Thermo Scientific). To examine mature miR-134-5 expression, 300 ng total RNA was reverse-transcribed to cDNA using the miRNA 1st-Strand cDNA synthesis kit (Agilent Technologies) according to the manufacturer’s protocol. For the RAN gene, 300 ng total RNA was reverse-transcribed to cDNA using the AffinityScript QPCR cDNA synthesis kit (Agilent Technologies). For the quantification of individual genes, cDNAs were diluted in water and quantified using Brilliant III Ultra-Fast SYBR Green QPCR Master Mix (Agilent Technologies) in an Agilent Mx3005P instrument. Primers specific for miR-134-5p (forward, 5′-TGTGACTGGTTGACCA-3′; reverse, universal primer) RAN (forward, 5′-GAAGCTCATTGGAGACCCTAAC-3′; reverse, 5′-CAACCTCTAAGTCGTGCTCATAC-3′) were used. The gene expression levels were normalized to 18s rRNA gene as an internal control.
Ingenuity pathway analysis and TargetScan analysis
QIAGEN’s Ingenuity pathway analysis (IPA; QIAGEN Redwood City; www.qiagen.com/ingenuity) was utilized to evaluate protein networks associated with PV replication in an effort to predict targets of miR-134 that may be involved in poliovirus infection and replication. TargetScan analysis (Whitehead Institute for Biomedical Research; http://www.targetscan.org/) was used to predict target transcripts via seed region complementarity. Pathway analysis and TargetScan analysis revealed many predicted targets, of interest was the nuclear transport system protein (RAN) because it has been previously published that another microRNA, miR-197, inhibited enterovirus 71 replication by targeting the RAN protein16.
Data normalization and statistical analysis
The current screen was examined using Z’-factor (1>Z’>0.5: Excellent assay; 0.5>Z’>0: acceptable) to evaluate its quality. The majority of our screen fell into a Z’ factor (0.5<Z’<1.0) which reflects high-quality of the primary screen. Afterwards, the primary screen data was normalized to the entire plate and generated the mean (μ) of the data to zero and the standard deviation (s.d.) to 1. To achieve a high-quality and robust screen, we used siTOX (GE Healthcare Dharmacon TOX™ Transfection Control, Cat. # D0015000120) to monitor the transfection efficiency; we also used a siRNA targeting poliovirus (CDC, provided by Dr Steve Oberste) to monitor silencing effects on poliovirus replication (see transfection control section). A non-targeting siRNA (GE Healthcare Dharmacon: Cat. # D-001810-0X) used as a negative control. All experiments were performed in at least two independent replicates with each experiment consisting of duplicates for each miRNA targeting a specific mRNA transcript for the gene of interest. ELISA absorbance values were normalized by correcting the raw data. The mean of the replicates where calculated and standardized using Z-score analysis. The mean of the wells treated with experimental miRNAs for each miRNA were compared to the mean of negative control treated wells. The Z-score was calculated by finding the difference between the normalized score and the mean of the population and dividing this by the standard deviation of the population. Positive hits from the primary screen are scored by Z-score>1.5 s.d.
All results are presented as means±s.e. Statistical analysis was done using the one-way ANOVA with Turkey’s multiple comparison at 95% confidence level. P-values<0.05 were considered statistically significant.
Data record 1
The miRNA mimic screen data presented is available at PubChem under NCBI PubChem BioAssay AID 1224906 (Data Citation 1: NCBI PubChem BioAssay 1224906). In this RNAi screen, miRNA mimics corresponding to 1,208 known miRNAs in the human genome were screened in HEp-2 cells for their regulatory effects against Sabin-2 poliovirus. One hundred eight miRNAs resulted in a substantial reduction of poliovirus replication relative to non-targeting control (z-scores≤−1.5). Forty-six miRNAs resulted in a substantial increase of poliovirus replication relative to non-targeting control (z-scores≥1.5) (Table 2). Included within this dataset are the hits which resulted in a standard z-score≤−0.5 and z-score≥0.5 compared to non-targeting control.
Data record 2
The miRNA inhibitor data is available at PubChem under NCBI PubChem BioAssay AID 1224851 (Data Citation 2: NCBI PubChem BioAssay 1224851). The top miRNA hits from the mimic screening assays were re-screened in HEp-2 cells, to eliminate false-positive hits. In this case, miRNA inhibitors were tested to determine if they induced a phenotype which correlated with that of the miRNA mimic results. Included within this dataset are the z-scores of all miRNAs inhibitors tested.
To establish a highly efficient miRNA transfection protocol in a high-throughput screening (HTS) fashion, we first investigated four individual DharmaFECT transfection reagents (DF1-4). We identified that DF4 is the most effective in gene silencing for both HEp-2. Further we performed the titration of the concentration of DF4 in both cell lines. In the case with 0.3% DF4 concentration, the GAPDH silencing was achieved >90%, and cell toxicity was not observed in either microscopy examination or MTT assay.
Cytotoxicity as a result of miRNA transfection was evaluated by CytoTox-Glo assay (Promega) according to manufacturer instructions. Briefly, HEp-2 cells were reverse transfected with miRNA mimics as described previously22. Forty-eight hours post-transfection cellular toxicity was evaluated. Values were normalized to siTOX control (100% cytotoxic). MiRNAs which elicited greater than 20% toxicity were excluded as is standard practice. In this study, we focused on the miRNA mimics screening, and observed some miR-induced cell death. Toxic miRNAs that lead to cell death including miR-1275, miR-129-3P, miR509, miR-1909, miR323-5P, miR-4265, miR-3661 were excluded from further studies. For the list of hits identified from miRNA mimics screening, we did not observe significant cell death for the corresponding miRNA inhibitors.
A high-quality RNAi screen integrates both excellent experimental design and computational strategies for quality control. A clear distinction between a positive control and a negative reference is paramount. In the current miRNA screen in HEp-2 cell line, a positive control siRNA specifically targeting poliovirus (Poliovirus-specific (VP1 & 3D) and a negative control (non-targeting siRNA) were clearly distinguished from each other in all 96-well plates transfected with siRNAs. siTOX (GE Healthcare Dharmacon TOX Transfection Control, Cat. # D0015000120) was used to serve as another indicator for transfection efficiency and a mock control used as background normalization.
As part of developing a screening assay with low variation and a strong signal to background ratio we conducted pilot studies to optimize screening conditions. These conditions included optimizing titration of miRNA and siRNAs used to determine the most effective concentrations. Assay responses to negative and positive miRNA and siRNA controls were also evaluated and optimized to determine baseline values and standard deviation value for the calculation of Z-scores. Z-scores were subsequently used to determine hits for further screening. Transfection efficiency was optimized via transfection with miRIDIAN microRNA Mimic housekeeping positive Control #2 (GAPDH) (Cat. # CP-001000-02) as well as the inclusion of siTOX transfection control as previously mentioned. MRNA transcription levels were evaluated by qPCR following miRNA transfection and compared to GAPDH control to confirm miRNA mediated mRNA knockdown. Positive controls for poliovirus screening were carefully selected and optimized (Fig. 6)23. The culmination of this data suggests high transfection efficiency, low variability and substantial positive control values concluding that our screening procedure is robust.
How to cite this article: Orr-Burks, N. L. et al. MicroRNA screening identifies miR-134 as a regulator of poliovirus and enterovirus 71 infection. Sci. Data 4:170023 doi: 10.1038/sdata.2017.23 (2017).
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Orr-Burks, N., Shim, B., Wu, W., Bakre, A., & Tripp, R. NCBI PubChem BioAssay 1224851 (2017)
We would like to thank Dr Steve Oberste, CDC, for providing the poliovirus strains used in these studies. The authors would like to thank the Georgia Research Alliance for supporting the studies.
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