- Open Access
5'PPP-RNA induced RIG-I activation inhibits drug-resistant avian H5N1 as well as 1918 and 2009 pandemic influenza virus replication
- Priya Ranjan1,
- Lakshmi Jayashankar1,
- Varough Deyde1,
- Hui Zeng1,
- William G Davis1,
- Melissa B Pearce1,
- John B Bowzard1,
- Mary A Hoelscher1,
- Victoria Jeisy-Scott1,
- Mayim E Wiens1,
- Shivaprakash Gangappa1,
- Larisa Gubareva1,
- Adolfo García-Sastre2,
- Jacqueline M Katz1,
- Terrence M Tumpey1,
- Takashi Fujita3Email author and
- Suryaprakash Sambhara1Email author
© Ranjan et al; licensee BioMed Central Ltd. 2010
- Received: 25 March 2010
- Accepted: 21 May 2010
- Published: 21 May 2010
Emergence of drug-resistant strains of influenza viruses, including avian H5N1 with pandemic potential, 1918 and 2009 A/H1N1 pandemic viruses to currently used antiviral agents, neuraminidase inhibitors and M2 Ion channel blockers, underscores the importance of developing novel antiviral strategies. Activation of innate immune pathogen sensor Retinoic Acid Inducible Gene-I (RIG-I) has recently been shown to induce antiviral state.
In the present investigation, using real time RT-PCR, immunofluorescence, immunoblot, and plaque assay we show that 5'PPP-containing single stranded RNA (5'PPP-RNA), a ligand for the intracytoplasmic RNA sensor, RIG-I can be used as a prophylactic agent against known drug-resistant avian H5N1 and pandemic influenza viruses. 5'PPP-RNA treatment of human lung epithelial cells inhibited replication of drug-resistant avian H5N1 as well as 1918 and 2009 pandemic influenza viruses in a RIG-I and type 1 interferon dependant manner. Additionally, 5'PPP-RNA treatment also inhibited 2009 H1N1 viral replication in vivo in mice.
Our findings suggest that 5'PPP-RNA mediated activation of RIG-I can suppress replication of influenza viruses irrespective of their genetic make-up, pathogenicity, and drug-sensitivity status.
- A549 Cell
- Influenza Virus
- H5N1 Virus
Annual influenza epidemics caused by influenza A and B viruses result in three to five million cases of severe illness with about 250,000 to 500,000 deaths globally every year. In the United States, complications from influenza infections result in approximately 250,000 hospitalizations and 36,000 deaths in an average year, with majority of the fatalities occurring among the elderly population . Influenza A viruses are further sub typed based on hemagglutinin (HA) and neuraminidase (NA) proteins present on the virion envelope and there are 16 HA and 9 NA types known among influenza A viruses [2, 3]. Frequent minor genetic changes, known as antigenic drift and the emergence of influenza A viruses with novel NA and/or HA subtypes, known as antigenic shift result in epidemics and pandemics respectively. In the 20th century, only viruses of the H1, H2 or H3 and N1 or N2 subtypes have caused sustained epidemics in humans. However, other subtypes namely H7, H9, and H5 which primarily cause infections and death among avian species have crossed the species barrier and caused mild to severe or fatal disease in humans . Since 2003, highly pathogenic avian influenza (HPAI) H5N1 viruses have expanded their geographical distribution and are currently endemic in domestic poultry and wild birds in approximately 60 countries on three continents . As of May 61, 2010, 498 human cases in 15 countries with a 60% mortality rate have been reported . Consequently, these viruses have the potential to cause a pandemic, if they acquire the ability for sustained transmission among humans [7, 8]. In fact we are in the midst of a pandemic as a result of sustained human-to-human transmission by a novel H1N1 virus containing the gene segments from avian, human, and swine influenza viruses to which people lack immunity [9–11].
Vaccination is the primary strategy for reducing the morbidity and mortality associated with human influenza [12–15]. However, the population at risk such as elderly, pediatric, transplant recipients, and others who are immunocompromised with either primary or secondary immunodeficiency disorders remain vulnerable despite vaccination as in case of avian influenza viral infection and children, adolescents, pregnant women, and those with underlying medical conditions as in case of 2009 H1N1 pandemic influenza virus infection . Therefore, the use of antiviral drugs is a crucial public health countermeasure for preventing and treating influenza, particularly in circumstances of increased incidence influenza infections when there is a vaccine mismatch or shortage, when vaccine usage is limited or non-existent, or when there is no effective vaccine available globally in the market as in the case of H5N1 virus infections. Currently, two classes of antiviral drugs are available to treat influenza infections: the M2 ion-channel blockers amantadine and rimantadine and the NA inhibitors oseltamivir and zanamivir [17–20]. However, the emergence of human seasonal, highly virulent H5N1 influenza viruses as well as 2009 H1N1 pandemic influenza viruses that are resistant to one or both the classes of drugs underscores the need for development of new generation drugs as well as other novel preventive and therapeutic strategies [13, 21–28].
The immune system has evolved to recognize and eliminate pathogens. A number of pathogen recognition receptor (PRRs) families are involved in pathogen sensing and can be present in the host as soluble molecules in tissue fluids and serum or as molecules on cell membranes, localized in various cellular compartments, or in the cytosol [29–31]. Recognition of pathogen-associated molecular patterns (PAMPs) by PRRs results in rapid induction of innate immune responses that include production of antiviral cytokines such as the type I interferons (IFN-I) as well as proinflammatory cytokines responsible for impairment of viral replication and induction of adaptive immune responses . The presence of viral RNA or DNA in cytosol is detected by retinoic acid inducible gene-I (RIG-I) and melanoma differentiation-associated gene 5 (MDA-5), DNA-dependent activator of IFN-regulator factors (DAI) or absent in melanoma 2 (AIM2) [33–36]. Several human viruses, including hepatitis C (HCV), vaccinia, Ebola, and influenza have evolved strategies to target and inhibit distinct steps in the early signaling events that lead to IFN-I induction, indicating the importance of IFN-I in the host's antiviral response [37–40]. In case of influenza viruses, we and others have shown that nonstructural protein 1 (NS1) inhibits the function of the RIG-I [41–44]. RIG-I is critical for the induction of an antiviral innate immune response against influenza virus and its C-terminal helicase domain contains the characteristic amino acid signature motif of many RNA binding proteins . The interaction of C-terminal domain with viral RNA either short double stranded RNA or 5'PPP-ssRNA with a panhandle structure facilitates its interaction with IPS-1 (interferon-β promoter stimulator 1) via its N-terminal CARD (caspase-recruitment domain) [42, 46–48]. Recent reports suggest various ligands for RIG-I including ssRNA and dsRNA that may require specific sequences or may not require a triphosphate on their 5'-termini [42, 46–53]. Despite the various reports that describe ligands and mechanisms of RIG-I mediated antiviral response there is no report that suggests that RIG-I activation can inhibit replication of influenza viruses irrespective of their genetic makeup, pathogenecity and drug-resistant status. In the present study, we investigated whether the evolutionarily conserved antiviral strategies such as the stimulation of RIG-I with 5'PPP-RNA inhibit the replication of these influenza viruses.
5'PPP-RNA inhibits the replication of 1918 pandemic virus as well as both wild-type and drug-resistant H5N1
Next we evaluated the prophylactic antiviral potential of 5'PPP-RNA against avian influenza H5N1 viruses with pandemic potential. A549 cells were transfected with 5'PPP-RNA or CIAP-RNA for 0, 24 or 48 hr, and infected with A/Vietnam/1203, an H5N1virus. Viral titers were determined 24 hr post-infection. As shown in Figure 1A(ii), A549 cells treated with 5'PPP-RNA showed antiviral effect after 24 hr of transfection. This effect was not seen in control or in CIAP-RNA transfected A549 cells. This inhibitory effect persisted even after 72 hr (data not shown) suggesting a sustained antiviral effect of 5'PPP-RNA.
Stockpiling of the antiviral drug, oseltamivir is one strategy for pandemic preparedness, but the emergence of oseltamivir-resistant H5N1 viruses would seriously impede these efforts. Hence, we also tested the ability of 5'PPP-RNA to inhibit the replication of drug-resistant A/Vietnam/1203/2004 viruses that include zanamivir- and oseltamivir-sensitive and adamantanes-resistant and adamantanes- and oseltamivir-resistant virus variants, A/VN/30408/2005 (H274Y) and A/VN/HN/30408/2005 (N294S). As shown in Figure 1B(i-iii), 5'PPP-RNA transfection in A549 cells significantly reduced the replication of all the three drug-resistant H5N1 viruses. A549 cells treated with CIAP-RNA did not have any impact on viral replication and viral titers were comparable to control. We also used NHBE cells in our studies with H5N1 infection, and similar antiviral effects of 5'PPP-RNA were observed (data not shown). Seasonal drug-resistant H1N1 and H3N2 and their wild-type counter parts were chosen to measure the efficacy of 5'PPP-RNA treatment on viral replication. Influenza viruses of different HA and NA and members of the same subtype have different replication efficiencies. The replication efficiencies of these viruses were well characterized in MDCK cells. As expected, 5'PPP-RNA treatment of A549 cells inhibited the replication of wild-type and drug-resistant human seasonal H1N1, H3N2 and B viruses (Additional file 1, Figure S1). In all cases, activation of RIG-I pathway by 5'PPP-RNA transfection inhibited viral replication by 1.5 to 3 logs. Furthermore, we investigated if the viruses that grew in the presence of 5'PPP-RNA treatment were escape mutants that developed resistance to type I interferon. As shown in Additional file 2, Figure S2, the viruses that grew in the presence of 5'PPP-RNA are still susceptible to 5'PPP-RNA treatment when tested subsequently.
5'PPP-RNA inhibits 2009 pandemic H1N1 viruses both in vitro and in vivo
5'PPP-RNA induced upregulation of IFNβ and RIG-I
Activation of the innate immune system is critical for the induction and maintenance of host antiviral defenses. However, viruses also have evolved mechanism(s) that circumvent host immune responses. Several studies, including our own have shown independently that non-structural protein (NS1) of influenza A viruses inhibits RIG-I function. We, therefore, investigated the expression of IFNβ and RIG-I as well as NS1 by real-time RT-PCR in 5'PPP-RNA or CIAP-RNA transfected A549 cells that were either uninfected or infected with H5N1 virus at an MOI of 0.1 for 24 hr following transfection. As shown in Figure 3C(i&ii), 5'PPP-RNA induced IFNβ and RIG-I induction remained unchanged in H5N1 infected A549 cells. H5N1 virus infection induced the expression of NS1 by 250-300-fold over uninfected A549 cells [Figure 3(iii)] and did not induce IFNβ and RIG-I and prior treatment with 5'PPP-RNA significantly inhibited viral NS1 expression. Similar effects were observed for 1918 infection in A549 cells (data not shown).
Involvement of RIG-I and type 1 interferon in 5'PPP-RNA induced antiviral effect
In vitro therapeutic potential of 5'PPP-RNA
Three influenza pandemics occurred during the 20th century, with varying degrees of severity; outcomes ranged from the high levels of illness and death observed during the 1918 Spanish flu pandemic (estimates of deaths range from 20 to 100 million) to the much lower levels observed during the pandemics of 1957 and 1968 (approximately one million deaths each) [54, 55]. Furthermore, the spread of highly pathogenic avian influenza viruses since 2004 has also intensified concern over the emergence of novel strains of influenza with pandemic potential as exemplified by the current pandemic caused by a triple reassortant virus . Since the vaccine was not available for use in the first wave of a pandemic, Oseltamivir, a neuraminidase inhibitor became the first choice for prophylactic and therapeutic intervention. The ongoing emergence of seasonal avian H5N1 as well as novel H1N1 pandemic influenza viruses that are resistant to one or other class of antiviral drugs underscores the fragility of the public health strategy to control seasonal influenza infections [28, 56, 57]. To overcome these challenges and improve preparedness against infections with oseltamivir-resistant viruses, developing novel antiviral prophylactic as well as therapeutic approaches that offer a broad spectrum approach and are independent of the genetic makeup of influenza viruses is absolutely critical.
In the present study, we explored the role of in vitro transcribed 5'PPP-RNA, a ligand for cytoplasmic RNA sensor, RIG-I, in antiviral innate immune response against a panel of influenza viruses including drug-resistant, potential pandemic as well as pandemic strains in human lung epithelial cells. The broad-spectrum prophylactic potential of 5'PPP-RNA against influenza viruses is clearly evident from our studies. 5'PPP-RNA significantly inhibited in vitro growth of not only wild-type drug-sensitive and resistant H5N1 strains with comparable efficacy but also highly pathogenic 1918 pandemic strain. We also included 2009 pandemic H1N1 viruses in our studies to see the effect of 5'PPP-RNA both in vitro and in vivo. Data shown Figure 2A clearly indicate that in vitro suppression level of A/California/08/09 was similar to that of other viruses used in this study. Furthermore, 5'PPP-RNA also inhibited A/California/08/09 viral replication in vivo in Balb/c mice. These data suggest that irrespective of type or subtypes, drug-susceptibility status, or in vivo virulence, the replication of influenza viruses was inhibited by 5'PPP-RNA. The dose and frequency of administration of 5'PPP-RNA may influence the extent of inhibition of viral replication.
Treatment with 5'PPP-RNA not only induced the expression of IFN-I but also upregulated RIG-I expression. 5'PPP-RNA induced expression of IFN-I and RIG-I was not affected by subsequent infection with H5N1 (Figure 3C) or 1918 pandemic influenza viruses (data not shown). Induction of these molecular regulators of innate immune pathway may be involved in the sustained action of the 5'PPP-RNA-induced antiviral effect.
Viruses have acquired mechanism(s) to escape host immune surveillance by inhibiting IFN induction pathways. The NS1 protein of Influenza A virus inhibits host antiviral defenses by direct interaction with RIG-I [41–44]. 5'PPP-RNA treated A549 cells infected with H5N1 virus showed significant reduction of NS1 mRNA expression as compared to controls, thereby limiting the ability of the virus to interfere with the host innate immune system. RIG-I-mediated antiviral effect by 5'PPP-RNA lasted for 48 hr which also correlates with sustained induction of IFN-I that lasted more than 48 hr as revealed by time-kinetics studies (data not shown). To test the role of RIG-I, we knocked down RIG-I expression using siRNA, which abrogated 5'PPP-RNA ability to induce IFNβ and to inhibit virus replication. Since, there is a significant increase in IFNβ in addition to RIG-I in 5'PPP-RNA treated lung epithelial cells, we investigated whether this effect is due to the action of IFN-I induced by initial interaction of 5'PPP-RNA with RIG-I. We abrogated the expression of IFNα/β-receptors of A549 cells using siRNA and infected them subsequently with A/New York/02/2001 virus. By knocking down the expression of IFNα/β receptors, we were unable to detect significant level of IFNβ and RIG-I induction following 5'PPP-RNA treatment and inhibitory effect on virus growth (Figure 4A&4B). These findings suggest the direct involvement of RIG-I-induced type I IFN in the 5'PPP-RNA mediated antiviral effect. Our data support the previous findings that IFN can act in an autocrine or paracrine manner to induce its own expression as well as other antiviral modulators to generate an antiviral state . Though type I interferon seems to be key player in antiviral action, systemic or local delivery of IFNβ may be toxic and may result in uncontrolled inflammation . Activation induced type I interferon is self-regulated by feedback mechanisms and prevents side effects.
To evaluate the therapeutic potential of 5'PPP-RNA, we treated pre-infected (with wild-type and drug-resistant A/New York/02/2001) A549 cells with 5'PPP-RNA at different time-points. We observed relatively weak antiviral effect of 5'PPP-RNA, when A549 cells were transfected with 5'PPP-RNA post 8 hr infection. Interestingly, at this time point we also observed significantly low RIG-I and IFNβ expression (Figure 5). These data again suggest the critical role of RIG-I and type I IFN expression which may have been suppressed due to NS1 expression at 8 hr post-infection.
The findings described herein demonstrate that understanding host innate immune functions at the molecular level is a most promising strategy to identify targets, such as RIG-I for developing newer classes of drugs. These novel approaches that boost host antiviral innate immune defenses are broad spectrum in nature, rather than virus-specific as they inhibited replication of wild-type and drug-resistant strains of seasonal and avian viruses as well as pandemic influenza viruses. Since these approaches are based on stimulating host antiviral defenses, the possibility of viruses developing resistance to this approach is remote as these defenses are evolutionarily conserved.
In vitro synthesis of 5'PPP-RNA
5'PPP-RNAs were synthesized using T7 RNA polymerase. Using annealed complimentary oligo nucleotides, a DNA template was constructed that contains a T7 RNA polymerase promoter followed by the sequence of interest (AGCUUAACCUGUCCUUCAA) to be transcribed [60, 61]. Twenty pmol of the DNA template were incubated with 25U T7 RNA polymerase, 40U RNase inhibitor in a buffer containing 40 mM Tris-Hcl (pH 8.0), 10 mM DTT, 2 mM spermidine-HCl, 20 mM MgCl2 and NTPs. DNA template was digested with DNase I and RNA was purified using phenol:chloroform extraction and ethanol precipitation. Size, integrity and single strandness of RNA was analyzed by RNase A digestion followed by gel electrophoresis. Calf intestine alkaline phosphatase (CIAP) treatment was performed to remove tri-phosphate groups from in vitro synthesized RNA. Briefly, 100 μg of in vitro transcribed RNA was treated with 150U of CIAP for 3 hr at 37°C in a buffer containing 50 mM Tris-HCl (pH 8.0), 0.1 mM EDTA and 50U of RNase inhibitor. RNA was purified as described above. Chemically synthesized RNA with same sequence and length that contains an OH-group at its 5'-end was purchased from Dharmacon (Lafayette, CO, USA).
T7 polymerase driven in vitro transcribed 5'-PPP-RNA has been shown to contain dsRNA as well that activates RIG-I [46, 48]. To investigate if our in vitro transcribe 5'PPP-RNA is single stranded RNA (ssRNA) and/or double stranded RNA,(dsRNA) we used RNase A treatment under the conditions that degrades ssRNA, but not dsRNA. This confirmed that in vitro transcribed RNA used in our study was RNA only (Additional file 3, Figure S3).
A549 cells were grown in DMEM (Life Technologies, Grand Island, NY) supplemented with 10% fetal bovine serum (FBS), 100? U/ml penicillin and 100 μg/ml streptomycin. Normal human bronchial epithelial (NHBE) cells (Base, Lonza, Switzerland) were maintained under the conditions and media specified by the supplier.
Seasonal viruses used in this study include the laboratory H1N1 strain A/Puerto Rico/8/34, wild-type H1N1 (A/Texas/36/91 and its oseltamivir-resistant variant H274Y; wild-type A/New York/02/2001 and its H274Y oseltamivir-resistant variant), H3N2 (adamantane-resistant A/Wisconsin/06/94, A30V and A/Wisconsin/12/90, L26F), and B viruses (wild-type B/Memphis/20/96 and its R152K mutant resistant to NA inhibitors zanamivir and oseltamivir), HPAI H5N1 viruses (zanamivir- and oseltamivir-sensitive and adamantane-resistant A/Vietnam/1203/2004 and, adamantane- and oseltamivir-resistant virus variants A/Vietnam/30408/2005 (H274Y), and A/Vietnam/HN30408/2005 (N294S),, 2009 pandemic H1N1 viruses, A/California/08/09 and A/Mexico/4482/09, and the reconstructed 1918 Spanish influenza pandemic virus (H1N1) generated by plasmid-based reverse genetics . All human and avian wild-type and drug-resistant viruses were obtained from the influenza division CDC repository.
5'PPP-RNA treatment and influenza viral infections
Cells were transfected with 2 μg of in vitro transcribed 5'PPP-RNA, chemically synthesized RNA or CIAP-treated RNA using Lipofectamine 2000. This dose was determined by dose-kinetics studies using 1, 2, 4 and 6 μg of RNA. After 24 hr, cells were infected with the different viruses used in this study in a 6-well plate. Unless specified, infection of cells was performed at a multiplicity of infection (MOI) of 0.1 with or without trypsin supplement. Each treatment was carried out in duplicate cultures. After 24 hr, cells were harvested for RNA and protein analysis and cell-culture supernatants were collected and stored at -80°C for determination of viral titer by plaque assay as described previously using MDCK cells. This time-point was determined by kinetics studies using PR8. To study the therapeutic potential of 5'PPP-RNA cells were infected with viruses first for 2, 4 or 8 hr followed by transfection with 5'PPP-RNA. Three independent experiments were performed at different times with each treatment carried out in duplicate cultures.
Real Time RT-PCR
Total RNA was isolated from cells using the RNAeasy kit (Qiagen, Valencia, CA, USA) and real time RT-PCR was conducted using a Stratagene Q3005 PCR machine for mRNA expression of RIG-I, IFNβ, NS1, and β-actin. For each sample, 2 μg of RNA was reverse transcribed using Superscript II Reverse Transcriptase (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's directions. Parallel reactions without reverse transcriptase were included as negative controls. Reverse transcription reactions (1/50th of each reaction) were analyzed in using syber green Q-PCR reagents (Stratagene, La Jolla, CA, USA). PCR condition was kept as 94°C for 15 s, annealing at 56°C for 30 s, and extension at 72°C for 30 s for a total of 45 cycles. The threshold cycle number for cDNA was normalized to that of β-actin mRNA, and the resulting value was converted to a linear scale. Data from three independent experiments were taken account for analysis. All data points fell into a normal distribution and there were no outliers.
Primer sets used for these studies are as follows:
IFNβ: forward 5'- TGG GAG GCT TGA ATA CTG CCT CAA -3'
reverse 5'- TCT CAT AGA TGG TCA ATG CGG CGT -3'
RIG-I: forward 5'- AAA CCA GAG GCA GAG GAA GAG CAA -3'
reverse 5'- TCG TCC CAT GTC TGA AGG CGT AAA -3'
NS1: forward 5'-AGA AAG TGG CAG GCC CTC TTT GTA-3'
reverse 5'-TGT CCT GGA AGA GAA GGC AAT GGT -3'
β-actin: forward 5'- ACC AAC TGG GAC GAC ATG GAG AAA -3'
reverse 5'- TAG CAC AGC CTG GAT AGC AAC GTA -3'
Cells were washed with chilled PBS and then lysed in 100 μl of ice-cold lysis buffer (50 mM Tris-Cl, pH 8.0, 150 mM NaCl, 10% v/v glycerol, 1% v/v Triton X-100, 2 mM EDTA, 1 mM PMSF, 20 μM leupeptin containing aprotinin 0.15 μg/ml) for 20 minutes at 4°C. The protein content of different samples was determined using a protein assay reagent (BioRad, Inc., CA, USA). Equal quantities of solubilized protein were resolved by 10% SDS-PAGE, blotted to nitrocellulose membrane and probed with the indicated primary antibodies. Anti-RIG-I was purchased from Axxora, LLC (San Diego, CA, USA). Anti-β-actin antibody was purchased from Sigma, St. Louis, MO, USA. Antibody signals were detected by chemiluminescence using secondary antibodies conjugated to horseradish peroxidase and an ECL detection kit (Amersham Biosciences, Inc., NJ, USA).
A549 cells grown on cover-slips were mock-transfected or transfected with 2 μg of 5'PPP-RNA or CIAP-RNA for 24 hr. Cell monolayers were then washed with cold PBS and fixed with 2% paraformaldehyde for 15 min at room temperature. Cells were permeablized with 0.05% saponin in PBS for 30 min at room temperature, and then blocked with blocking buffer (1% BSA, 5% normal goat serum and 0.05% saponin in PBS) at room temperature. Cells were incubated with primary antibodies (1 μg/ml) at 4°C overnight, and were washed 3 times with wash buffer (0.05% saponin in PBS). Cell monolayers were further incubated with secondary antibodies (Alexa 594 or 488) in blocking buffer for 1 hr at room temperature followed by three washes with buffer. To stain nuclei, cells were incubated with Hoechst dye (5 μM in PBS containing 0.05% saponin). Cells were further washed (3 times) with PBS, and were mounted on slides using Prolong antifade mounting media (Invitrogen, Carlsbad, CA, USA) and were observed under a Zeiss LSM 510 fluorescence microscope.
In vivo studies
Female Balb/c mice 6-12 weeks old purchased from Jackson Laboratories were intravenously injected 100 μg of 5'PPP-RNA, capped 5'-RNA or PBS complexed with in vivo-jetPEI according to manufacturer's protocol (Polyplus-transfection Inc, San Diego, CA USA) in a volume of 200 μl for 4 days. On day 1, mice were challenged intranasaly with 1000 MID50 of 2009 pandemic virus (A/Mexico/4482/09). A separate group of animals that received only 5'PPP-RNA complexed with in vivo-jetPEI without viral challenge were observed to determine changes in body weight and activity. Lungs from control and treated challenged animals were collected on day 4 to determine viral titers using MDCK cells as described earlier.
To determine the statistical significance among the 5'PPP-RNA or CIAP-RNA treated and untreated groups, we used Analysis of variance and a value of P < 0.05 was considered significant. All data points were included in the analysis and there were no outliers.
We thank Alexander Klimov and Nancy Cox for their advice and critical reading of this manuscript. These studies are funded by a grant awarded to SS by National Vaccine Program Office, and by NIAID grants RO1 AI46954, U19 AI62623, P01 AI058113, U19 AI83025, and CRIP (Center for Research on Influenza Pathogenesis, NIAID contract number HHSN266200700010C to AG-S.
The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the funding agency or Centers for Disease Control and Prevention.
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